Antibiotic resistance

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Antibiotic resistance tests: The bacteria in the culture on the left are susceptible to the antibiotics contained in the white paper discs. The bacteria in the culture on the right are resistant to most of the antibiotics.

Antibiotic resistance is a form of drug resistance whereby some (or, less commonly, all) sub-populations of a microorganism, usually a bacterial species, are able to survive after exposure to one or more antibiotics; pathogens resistant to multiple antibiotics are considered multidrug resistant (MDR) or, more colloquially, superbugs.[1]

Antibiotic resistance is a serious and growing phenomenon in contemporary medicine and has emerged as one of the pre-eminent public health concerns of the 21st century, in particular as it pertains to pathogenic organisms (the term is especially relevant to organisms that cause disease in humans). In the simplest cases, drug-resistant organisms may have acquired resistance to first-line antibiotics, thereby necessitating the use of second-line agents. Typically, a first-line agent is selected on the basis of several factors including safety, availability, and cost; a second-line agent is usually broader in spectrum, has a less favourable risk-benefit profile, and is more expensive or, in dire circumstances, may be locally unavailable. In the case of some MDR pathogens, resistance to second- and even third-line antibiotics is, thus, sequentially acquired, a case quintessentially illustrated by Staphylococcus aureus in some nosocomial settings. Some pathogens, such as Pseudomonas aeruginosa, also possess a high level of intrinsic resistance.

It may take the form of a spontaneous or induced genetic mutation, or the acquisition of resistance genes from other bacterial species by horizontal gene transfer via conjugation, transduction, or transformation. Many antibiotic resistance genes reside on transmissible plasmids, facilitating their transfer. Exposure to an antibiotic naturally selects for the survival of the organisms with the genes for resistance. In this way, a gene for antibiotic resistance may readily spread through an ecosystem of bacteria. Antibiotic-resistance plasmids frequently contain genes conferring resistance to several different antibiotics. This is not the case for Mycobacterium tuberculosis, the bacteria that causes Tuberculosis, since evidence is lacking for whether these bacteria have plasmids.[2] Also M. tuberculosis lack the opportunity to interact with other bacteria in order to share plasmids.[2][3]

Genes for resistance to antibiotics, like the antibiotics themselves, are ancient.[4] However, the increasing prevalence of antibiotic-resistant bacterial infections seen in clinical practice stems from antibiotic use both within human medicine and veterinary medicine. Any use of antibiotics can increase selective pressure in a population of bacteria to allow the resistant bacteria to thrive and the susceptible bacteria to die off. As resistance towards antibiotics becomes more common, a greater need for alternative treatments arises. However, despite a push for new antibiotic therapies, there has been a continued decline in the number of newly approved drugs.[5] Antibiotic resistance therefore poses a significant problem.

The growing prevalence and incidence of infections due to MDR pathogens is epitomised by the increasing number of familiar acronyms used to describe the causative agent and sometimes the infection; of these, MRSA is probably the most well-known, but others including VISA (vancomycin-intermediate S. aureus), VRSA (vancomycin-resistant S. aureus), ESBL (Extended spectrum beta-lactamase), VRE (Vancomycin-resistant Enterococcus) and MRAB (Multidrug-resistant A. baumannii) are prominent examples. Nosocomial infections overwhelmingly dominate cases where MDR pathogens are implicated, but multidrug-resistant infections are also becoming increasingly common in the community.

There were low levels of preexisting antibiotic-resistant bacteria before the widespread use of antibiotics,[6] [7] evolutionary pressure from their use has played a role in the development of multidrug-resistant varieties and the spread of resistance between bacterial species.[8] In medicine, the major problem of the emergence of resistant bacteria is due to misuse and overuse of antibiotics.[9] In some countries, antibiotics are sold over the counter without a prescription, which also leads to the creation of resistant strains. Other practices contributing to resistance include antibiotic use in livestock feed.[10][11] Household use of antibacterials in soaps and other products, although not clearly contributing to resistance, is also discouraged (as not being effective at infection control).[12] Unsound practices in the pharmaceutical manufacturing industry can also contribute towards the likelihood of creating antibiotic-resistant strains.[13] The procedures and clinical practice during the period of drug treatment are frequently flawed — usually no steps are taken to isolate the patient to prevent re-infection or infection by a new pathogen, negating the goal of complete destruction by the end of the course.[14] (see Healthcare-associated infections and Infection control)

Certain antibiotic classes are highly associated with colonisation with "superbugs" compared to other antibiotic classes. A superbug, also called multiresistant, is a bacterium that carries several resistance genes.[15] The risk for colonisation increases if there is a lack of susceptibility (resistance) of the superbugs to the antibiotic used and high tissue penetration, as well as broad-spectrum activity against "good bacteria". In the case of MRSA, increased rates of MRSA infections are seen with glycopeptides, cephalosporins, and especially quinolones.[16][17] In the case of colonisation with Clostridium difficile, the high-risk antibiotics include cephalosporins and in particular quinolones and clindamycin.[18][19]

Of antibiotics used in the United States in 1997, half were used in humans and half in animals.[20]

Natural occurrence[edit]

There is evidence that naturally occurring antibiotic resistance is common.[21] The genes that confer this resistance are known as the environmental resistome.[21] These genes may be transferred from non-disease-causing bacteria to those that do cause disease, leading to clinically significant antibiotic resistance.[21]

In 1952, an experiment conducted by Joshua and Esther Lederberg showed that penicillin-resistant bacteria existed before penicillin treatment.[22] While experimenting at the University of Wisconsin-Madison, Joshua Lederberg and his graduate student Norton Zinder also demonstrated preexistent bacterial resistance to streptomycin.[23] In 1962, the presence of penicillinase was detected in dormant Bacillus licheniformis endospores, revived from dried soil on the roots of plants, preserved since 1689 in the British Museum.[24][25][26] Six strains of Clostridium, found in the bowels of William Braine and John Hartnell (members of the Franklin Expedition) showed resistance to cefoxitin and clindamycin.[27] It was suggested that penicillinase may have emerged as a defense mechanism for bacteria in their habitats, such as the case of penicillinase-rich Staphylococcus aureus, living with penicillin-producing Trichophyton, however this was deemed circumstantial.[26] Search for a penicillinase ancestor has focused on the class of proteins that must be a priori capable of specific combination with penicillin.[28] The resistance to cefoxitin and clindamycin in turn was attributed to Braine's and Hartnell's contact with microorganisms that naturally produce them or random mutation in the chromosomes of Clostridium strains.[27] Nonetheless there is evidence that heavy metals and some pollutants may select for antibiotic-resistant bacteria, generating a constant source of them in small numbers.[29]

In medicine[edit]

In 1945, in his Nobel lecture "Penicillin," Alexander Fleming warned against the use of sub‐therapeutic doses of antibiotics – "bought by anyone in the shops" without a prescription:

"The time may come when penicillin can be bought by anyone in the shops. Then there is the danger that the ignorant man may easily underdose himself and by exposing his microbes to non‐lethal quantities of the drug make them resistant. Here is a hypothetical illustration. Mr. X. has a sore throat. He buys some penicillin and gives himself, not enough to kill the streptococci but enough to educate them to resist penicillin. He then infects his wife. Mrs. X gets pneumonia and is treated with penicillin. As the streptococci are now resistant to penicillin the treatment fails. Mrs. X dies. Who is primarily responsible for Mrs. X’s death?"[30]

Inappropriate prescribing of antibiotics has been attributed to a number of causes, including people insisting on antibiotics, physicians prescribing them as they feel they do not have time to explain why they are not necessary, and physicians not knowing when to prescribe antibiotics or else overly cautious for medical legal reasons.[31] For example, a third of people believe that antibiotics are effective for the common cold,[32] and the common cold is the most common reasons antibiotics are prescribed[33] even though antibiotics are completely useless against viruses.

The number of persons inappropriately prescribed antibiotics is a greater factor in the increasing rates of bacterial resistance rather than non-compliance with antibiotic protocol among those prescribed the drugs. However, the non-compliance rate is high.[34] A single dose of antibiotics leads to a greater risk of resistant organisms to that antibiotic in the person for up to a year.[35]

Antibiotic resistance has been shown to increase with duration of treatment; therefore, as long as a clinically effective lower limit is observed (that depends upon the organism and antibiotic in question), the use by the medical community of shorter courses of antibiotics is likely to decrease rates of resistance, reduce cost, and have better outcomes due to fewer complications such as C. difficile infection and diarrhea.[36][37][38][39][40][41][42][43] In some situations a short course is inferior to a long course.[44] One study found that with one antibiotic a short course was more effective, but with a different antibiotic, a longer course was more effective.[45]

Advice to always complete a course of antibiotics is not based on strong evidence, and some researchers discourage the use of the prescription label that states “Finish all this medication unless otherwise directed by prescriber.” Often, antibiotics can be safely stopped 72 hours after symptoms resolve.[46] However, some infections require treatment long after symptoms are gone, and in all cases, an insufficient course of antibiotics may lead to relapse (with an infection that is now more antibiotic resistant).[47] Doctors must provide instructions to patients so they know when it is safe to stop taking a prescription, since patients may feel better before the infection is eradicated. Some researchers advocate doctors' using a very short course of antibiotics, reevaluating the patient after a few days, and stopping treatment if there are no longer clinical signs of infection.[48]

A large number of people do not finish a course of antibiotics primarily because they feel better (varying from 10% to 44%, depending on the country).[49] Compliance with once-daily antibiotics is better than with twice-daily antibiotics.[50] Patients taking less than the required dosage or failing to take their doses within the prescribed timing results in decreased concentration of antibiotics in the bloodstream and tissues, and, in turn, exposure of bacteria to suboptimal antibiotic concentrations increases the frequency of antibiotic resistant organisms.[51]

Antibiotic-tolerant states may depend on physiological adaptations without direct connections to antibiotic target activity or to drug uptake, efflux, or inactivation.

Poor hand hygiene by hospital staff has been associated with the spread of resistant organisms,[52] and an increase in hand washing compliance results in decreased rates of these organisms.[53]

The improper use of antibiotics and therapeutic treatments can often be attributed to the presence of structural violence in particular regions. Socioeconomic factors such as race and poverty affect the accessibility of and adherence to drug therapy. The efficacy of treatment programs for these drug-resistant strains depends on whether or not programmatic improvements take into account the effects of structural violence.[54]

Role of other animals[edit]

The emergence of antibiotic-resistant microorganisms in human medicine is primarily the result of the use of antibiotics in humans, although the use of antibiotics in animals is also partly responsible.[55]

Antibiotic drugs are used in animals that are intended for human consumption, such as cattle, pigs, chickens, fish, etc. Traditionally, there has been extensive use of antibiotics in animal husbandry. Many of these drugs are not considered significant drugs for use in humans, because of their lack of either efficacy or purpose in humans (such as the use of ionopores in ruminants[56]), or because that drug has gone out of use in humans (such as the decline in use of sulfa drugs due to widespread allergic reactions and antibiotic resistance among human pathogens). Historically, regulation of antibiotic use in food animals has been limited to limiting drug residues in meat, egg, and milk products, rather than concern over the development of antibiotic resistance. This mirrors the primary concerns in human medicine, where, in general, researchers and doctors were more concerned about effective but non-toxic doses of drugs rather than antibiotic resistance.

The resistant bacteria in animals due to antibiotic exposure can be transmitted to humans via three pathways, those being through the consumption of animal products (milk, meat, eggs, etc.), from close or direct contact with animals or other humans, or through the environment.[57] In first pathway, many food preservation methods are available in order to eliminate, decrease, or prevent the growth of bacteria. Evidence for the transfer of antibiotic- resistant microorganisms from animals to humans has been scant, and most evidence shows that pathogens of concern in human populations originated in humans and are maintained there, with rare cases of transference to humans.[58][59] The use of antibiotics in animals can be divided in different use patterns depending on what is its purpose. The most accepted classification discriminates the use of antibiotics as therapeutic, prophylactic, metaphylactic, and growth promotion.[60] The first three options are considered valid for therapeutic purposes in contrast with the fourth option that is considered as with non-therapeutic purposes. All these patterns predispose the exhibition of mechanisms of bacterial resistance due the proper use or misuse of antibiotics, since antibiotic resistance is a natural evolutionary process.

The World Health Organization concluded that inappropriate use of antibiotics in animal husbandry is an underlying factor that contributes to the emergence and spread of antibiotic-resistant germs, and the use of antibiotics as growth promoters in animal feeds should be prohibited, in the absence of risk assessments. Regarding this matter, the OIE has added to the Terrestrial Animal Health Code a series of guidelines with recommendations to its members for the creation and harmonization of national antimicrobial resistance surveillance and monitoring programs,[61] monitoring of the quantities of antibiotics used in animal husbandry,[62] and recommendations to ensure the proper and prudent use of antibiotic substances. Another guideline introduced in the terrestrial Animal Health Code is the implementation of methodologies that help to establish risk factors associated with this worldwide concern. The OIE concluded that risk assessments should be performed in order to assess, manage and define the possible health risks of antibiotic resistance in human and animal populations.[63]

In the world, the use of antibiotics in animals is widely accepted. As in human medicine, antibiotics can be bought without prescription and can be used in pets and livestock without veterinary supervision. Bacteria remaining in these animals are likely to be resistant to the antibiotics used, and may be passed into the environment by the excretion and secretion of materials such as milk, feces, urine, saliva, semen, lochia, etc. The actual impact of these resistant organisms depends on their specific type and the animal or organism they henceforth infect. Some organisms, such as tetanus, are toxic regardless of their antibiotic-resistant status. (It is useful to remember that antibiotics are not used in treatment of all diseases caused by bacteria. Tetanus, as an example, is prevented by vaccine and is extremely difficult to treat once symptoms appear.)

In 1998, European Union health ministers voted to ban four antibiotics widely used to promote animal growth (despite their scientific panel's recommendations). Regulation banning the use of antibiotics in European feed, with the exception of two antibiotics in poultry feeds, became effective in 2006.[64] In Scandinavia, there is evidence that the ban has led to a lower prevalence of antimicrobial resistance in (nonhazardous) animal bacterial populations.[65] However, a corresponding change in antibiotic-resistance cases among humans has not yet been demonstrated.

In the United States[edit]

In the United States, the United States Department of Agriculture (USDA) and the Food and Drug Administration (FDA) collect data on antibiotic use in animals and humans.[66] In research studies, occasional animal-to-human spread of drug-resistant organisms has been demonstrated. Antibiotics and other drugs are used in U.S. animal feed to promote animal health.[11][67] In particular, poultry feed and water is a common route of administration of drugs, due to unacceptable death and distress when drugs are administered by handling animals individually. In general, animals that appear ill are not permitted to be slaughtered for human consumption in the United States.

Growing U.S. consumer concern about using antibiotics in animal feed has led to a niche market of "antibiotic-free" animal products, but this small market is unlikely to change entrenched, industry-wide practices.[68]

In 2001, the Union of Concerned Scientists estimated that greater than 70% of the antibiotics used in the U.S. are given to food animals (for example, chickens, pigs, and cattle), in the absence of disease.[69] The amounts given are termed "sub-therapeutic", i.e., insufficient to combat disease. Despite no diagnosis of disease, the administration of these drugs (most of which are not significant to human medicine) results in decreased mortality and morbidity and increased growth in the animals so treated. It is theorized that sub-therapeutic dosages kills some, but not all, of the bacterial organisms in the animal — likely leaving those that are naturally antibiotic-resistant. Studies have shown, however, that, in essence, the overall population levels of bacteria are unchanged; only the mix of bacteria is affected.[citation needed]

Thus, the actual mechanism by which sub-therapeutic antibiotic feed additives serve as growth promoters is unclear. Some people have speculated that animals and fowl may have sub-clinical infections, which are cured by low levels of antibiotics in feed, thereby allowing the creatures to thrive; but no convincing evidence has been advanced for this theory. As the bacterial load in an animal is essentially unchanged by use of antibiotic feed additives, the mechanism of growth promotion is possible to be something other than "killing off the bad bugs."

In 2000, the FDA announced their intention to revoke approval of fluoroquinolone use in poultry production because of substantial evidence linking it to the emergence of fluoroquinolone-resistant Campylobacter infections in humans. The final decision to ban fluoroquinolones from use in poultry production was made in 2006 because of challenges from the food animal and pharmaceutical industries.[70] Fluroquinolones have been banned from extra-label use in food animals in the USA since 2007. However, they remain widely used in companion and exotic animals.

In 2001, National Hog Farmer magazine warned U.S. producers that C. difficile "is sweeping the industry, killing many piglets" (Neutkens D; "New Clostridium Claiming Baby Pigs"). In 2006, a study by the USDA's National Animal Health Monitoring System further investigated the prevalence of C. difficile in hog farms. The study, which covered hog farms of a size typical of those comprising 94% of US swine, found the prevalence of C. difficile was "relatively low (11.4%)" and that there was no difference in region or in size of farm.[71] Human infection with C. difficile (either drug-resistant or not) is most commonly associated with the use of strong antibiotics in hospitalized humans, and is not associated with humans in contact with farm animals.

During 2007, two federal bills (S. 549[72] and H.R. 962[73]) aimed at phasing out "nontherapeutic" antibiotics in U.S. food animal production. The Senate bill, introduced by Sen. Edward "Ted" Kennedy, died. The House bill, introduced by Rep. Louise Slaughter, died after being referred to Committee.

In the United States, evidence of emergence of antibiotic-resistant bacterial strains in livestock was determined by the FDA in 1977. However, the long-established practice of permitting OTC sales of antibiotics (including penicillin and other drugs) to lay animal owners for administration to their own animals continued in all states. In March 2012, the United States District Court for the Southern District of New York, ruling in an action brought by the Natural Resources Defense Council and others, ordered the FDA to revoke approvals for the use of antibiotics in livestock that violated FDA regulations.[74] On April 11, 2012 the FDA announced a voluntary program to phase out unsupervised use of drugs as feed additives and convert approved over-the-counter uses for antibiotics to prescription use only, requiring veterinarian supervision of their use and a prescription.[75][76] In December 2013, the FDA announced the commencement of these steps to phase out the use of antibiotics for the purposes of promoting livestock growth.[77]

Environmental impact[edit]

Antibiotics have been polluting the environment since their introduction through human waste (medication, farming), animals, and the pharmaceutical industry.[78] Along with antibiotic waste, resistant bacteria follow, thus introducing antibiotic-resistant bacteria into the environment. As bacteria replicate quickly, the resistant bacteria that enter the environment replicate their resistance genes as they continue to divide. In addition, bacteria carrying resistance genes have the ability to spread those genes to other species via horizontal gene transfer. Therefore, even if the specific antibiotic is no longer introduced into the environment, antibiotic-resistance genes will persist through the bacteria that have since replicated without continuous exposure.[78]

A study done of the Poudre River implicated wastewater treatment plants, as well as animal-feeding operations in the dispersal of antibiotic-resistance genes into the environment.[79] This research was done using molecular signatures in order to determine the sources, and the location at the Poudre River was chosen due to lack of other anthropogenic influences upstream. The study indicates that monitoring of antibiotic-resistance genes may be useful in determining not only the point of origin of their release but also how these genes persist in the environment. In addition, studying physical and chemical methods of treatment may alleviate pressure of antibiotic-resistance genes in the environment, and thus their entry back into human contact.

Mechanisms of antibiotic resistance[edit]

Schematic representation of how antibiotic resistance evolves via natural selection. The top section represents a population of bacteria before exposure to an antibiotic. The middle section shows the population directly after exposure, the phase in which selection took place. The last section shows the distribution of resistance in a new generation of bacteria. The legend indicates the resistance levels of individuals.
Diagram depicting antibiotic resistance through alteration of the antibiotic's target site, modeled after MRSA's resistance to penicillin. Beta-lactam antibiotics permanently inactivate PBP enzymes, which are essential for bacterial life, by permanently binding to their active sites. MRSA, however, expresses a PBP that does not allow the antibiotic into its active site.

Antibiotic resistance can be a result of horizontal gene transfer,[80] and also of unlinked point mutations in the pathogen genome at a rate of about 1 in 108 per chromosomal replication. The antibiotic action against the pathogen can be seen as an environmental pressure. Those bacteria with a mutation that allows them to survive live to reproduce. They then pass this trait to their offspring, which leads to the evolution of a fully resistant colony.

The four main mechanisms by which microorganisms exhibit resistance to antimicrobials are:

  1. Drug inactivation or modification: for example, enzymatic deactivation of penicillin G in some penicillin-resistant bacteria through the production of β-lactamases.
  2. Alteration of target site: for example, alteration of PBP—the binding target site of penicillins—in MRSA and other penicillin-resistant bacteria
  3. Alteration of metabolic pathway: for example, some sulfonamide-resistant bacteria do not require para-aminobenzoic acid (PABA), an important precursor for the synthesis of folic acid and nucleic acids in bacteria inhibited by sulfonamides, instead, like mammalian cells, they turn to using preformed folic acid.
  4. Reduced drug accumulation: by decreasing drug permeability or increasing active efflux (pumping out) of the drugs across the cell surface[81]

There are three known mechanisms of fluoroquinolone resistance. Some types of efflux pumps can act to decrease intracellular quinolone concentration.[82] In Gram-negative bacteria, plasmid-mediated resistance genes produce proteins that can bind to DNA gyrase, protecting it from the action of quinolones. Finally, mutations at key sites in DNA gyrase or topoisomerase IV can decrease their binding affinity to quinolones, decreasing the drug's effectiveness.[83] Research has shown the bacterial protein LexA may play a key role in the acquisition of bacterial mutations giving resistance to quinolones and rifampicin.[84]

Antibiotic resistance can also be introduced artificially into a microorganism through laboratory protocols, sometimes used as a selectable marker to examine the mechanisms of gene transfer or to identify individuals that absorbed a piece of DNA that included the resistance gene and another gene of interest. A recent study demonstrated that the extent of horizontal gene transfer among Staphylococcus is much greater than previously expected—and encompasses genes with functions beyond antibiotic resistance and virulence, and beyond genes residing within the mobile genetic elements.[85]

For a long time, it has been thought that, for a microorganism to become resistant to an antibiotic, it must be in a large population. However, recent findings show that there is no necessity of large populations of bacteria for the appearance of antibiotic resistance. We know now that small populations of E.coli in an antibiotic gradient can become resistant. Any heterogeneous environment with respect to nutrient and antibiotic gradients may facilitate the development of antibiotic resistance in small bacterial populations and this is also true for the human body. Researchers hypothesize that the mechanism of resistance development is based on four SNP mutations in the genome of E.coli produced by the gradient of antibiotic. These mutations confer the bacteria emergence of antibiotic resistance.

A common misconception is that a person can become resistant to certain antibiotics. It is a strain of microorganism that can become resistant, not a person's body.[86][87]

Resistant pathogens[edit]

Staphylococcus aureus[edit]

Staphylococcus aureus (colloquially known as "Staph aureus" or a "Staph infection") is one of the major resistant pathogens. Found on the mucous membranes and the human skin of around a third of the population, it is extremely adaptable to antibiotic pressure. It was one of the earlier bacteria in which penicillin resistance was found—in 1947, just four years after the drug started being mass-produced. Methicillin was then the antibiotic of choice, but has since been replaced by oxacillin due to significant kidney toxicity. Methicillin-resistant Staphylococcus aureus (MRSA) was first detected in Britain in 1961, and is now "quite common" in hospitals. MRSA was responsible for 37% of fatal cases of sepsis in the UK in 1999, up from 4% in 1991. Half of all S. aureus infections in the US are resistant to penicillin, methicillin, tetracycline and erythromycin.

This left vancomycin as the only effective agent available at the time. However, strains with intermediate (4-8 μg/ml) levels of resistance, termed glycopeptide-intermediate Staphylococcus aureus (GISA) or vancomycin-intermediate Staphylococcus aureus (VISA), began appearing in the late 1990s. The first identified case was in Japan in 1996, and strains have since been found in hospitals in England, France and the US. The first documented strain with complete (>16 μg/ml) resistance to vancomycin, termed vancomycin-resistant Staphylococcus aureus (VRSA) appeared in the United States in 2002.[88] However, in 2011, a variant of vancomycin has been tested that binds to the lactate variation and also binds well to the original target, thus reinstating potent antimicrobial activity.[89]

A new class of antibiotics, oxazolidinones, became available in the 1990s, and the first commercially available oxazolidinone, linezolid, is comparable to vancomycin in effectiveness against MRSA. Linezolid-resistance in S. aureus was reported in 2001.[90]

Community-acquired MRSA (CA-MRSA) has now emerged as an epidemic that is responsible for rapidly progressive, fatal diseases, including necrotizing pneumonia, severe sepsis, and necrotizing fasciitis.[91] MRSA is the most frequently identified antimicrobial drug-resistant pathogen in US hospitals. The epidemiology of infections caused by MRSA is rapidly changing. In the past 10 years[when?], infections caused by this organism have emerged in the community. The two MRSA clones in the United States most closely associated with community outbreaks, USA400 (MW2 strain, ST1 lineage) and USA300, often contain Panton-Valentine leukocidin (PVL) genes and, more frequently, have been associated with skin and soft tissue infections. Outbreaks of CA-MRSA infections have been reported in correctional facilities, among athletic teams, among military recruits, in newborn nurseries, and among men that have sex with men. CA-MRSA infections now appear endemic in many urban regions and cause most CA-S. aureus infections.[92]

Streptococcus and Enterococcus[edit]

Streptococcus pyogenes (Group A Streptococcus: GAS) infections can usually be treated with many different antibiotics. Early treatment may reduce the risk of death from invasive group A streptococcal disease. However, even the best medical care does not prevent death in every case. For those with very severe illness, supportive care in an intensive-care unit may be needed. For persons with necrotizing fasciitis, surgery often is needed to remove damaged tissue.[93] Strains of S. pyogenes resistant to macrolide antibiotics have emerged; however, all strains remain uniformly susceptible to penicillin.[94]

Resistance of Streptococcus pneumoniae to penicillin and other beta-lactams is increasing worldwide. The major mechanism of resistance involves the introduction of mutations in genes encoding penicillin-binding proteins. Selective pressure is thought to play an important role, and use of beta-lactam antibiotics has been implicated as a risk factor for infection and colonization. S. pneumoniae is responsible for pneumonia, bacteremia, otitis media, meningitis, sinusitis, peritonitis and arthritis.[94]

Multidrug-resistant Enterococcus faecalis and Enterococcus faecium are associated with nosocomial infections.[95] Among these strains, penicillin-resistant Enterococcus was seen in 1983, vancomycin-resistant Enterococcus in 1987, and linezolid-resistant Enterococcus in the late 1990s.[citation needed]

Pseudomonas aeruginosa[edit]

Pseudomonas aeruginosa is a highly prevalent opportunistic pathogen. One of the most worrisome characteristics of P. aeruginosa is its low antibiotic susceptibility, which is attributable to a concerted action of multidrug efflux pumps with chromosomally encoded antibiotic resistance genes (for example, mexAB-oprM, mexXY, etc.) and the low permeability of the bacterial cellular envelopes.[96] Pseudomonas aeruginosa has the ability to produce HAQs and it has been found that HAQs have prooxidant effects, and overexpressing modestly increased susceptibility to antibiotics. The study experimented with the Pseudomonas aeruginosa biofilms and found that a disruption of relA and spoT genes produced an inactivation of the Stringent response (SR) in cells with nutrient limitation, which provides cells be more susceptible to antibiotics.[97]

Clostridium difficile[edit]

Clostridium difficile is a nosocomial pathogen that causes diarrheal disease in hospitals world wide.[98][99] Clindamycin-resistant C. difficile was reported as the causative agent of large outbreaks of diarrheal disease in hospitals in New York, Arizona, Florida and Massachusetts between 1989 and 1992.[100] Geographically dispersed outbreaks of C. difficile strains resistant to fluoroquinolone antibiotics, such as ciprofloxacin and levofloxacin, were also reported in North America in 2005.[101]

Salmonella and E. coli[edit]

Infection with Escherichia coli and Salmonella can result from the consumption of contaminated food and water. When both bacteria are spread, serious health conditions arise. Many people are hospitalized each year after becoming infected, with some dying as a result. Since 1993, some strains of E. coli have become resistant to multiple types of fluoroquinolone antibiotics.[citation needed]

Acinetobacter baumannii[edit]

On November 5, 2004, the Centers for Disease Control and Prevention (CDC) reported an increasing number of Acinetobacter baumannii bloodstream infections in patients at military medical facilities in which service members injured in the Iraq/Kuwait region during Operation Iraqi Freedom and in Afghanistan during Operation Enduring Freedom were treated. Most of these showed multidrug resistance (MRAB), with a few isolates resistant to all drugs tested.[102][103]

Klebsiella pneumoniae[edit]

Klebsiella pneumoniae carbapenemase (KPC)-producing bacteria are a group of emerging highly drug-resistant Gram-negative bacilli causing infections associated with significant morbidity and mortality whose incidence is rapidly increasing in a variety of clinical settings around the world. Carbapenem antibiotics (heretofore often the treatment of last resort for resistant infections) are generally not effective against KPC-producing organisms.[104]

Mycobacterium tuberculosis[edit]

Tuberculosis is increasing across the globe, especially in developing countries, over the past few years. TB resistant to antibiotics is called MDR TB (Multidrug Resistant TB). Globally, MDR TB causes 150,000 deaths annually.[105] The rise of the HIV/AIDS epidemic has contributed to this.[106]

TB was considered one of the most prevalent diseases, and did not have a cure until the discovery of Streptomycin by Selman Waksman in 1943.[107] However, the bacteria soon developed resistance. Since then, drugs such as isoniazid and rifampin have been used. M. tuberculosis develops resistance to drugs by spontaneous mutations in its genomes. Resistance to one drug is common, and this is why treatment is usually done with more than one drug. Extensively Drug-Resistant TB (XDR TB) is TB that is also resistant to the second line of drugs.[106][108]

Resistance of Mycobacterium tuberculosis to isoniazid, rifampin, and other common treatments has become an increasingly relevant clinical challenge. (For more on Drug-Resistant TB, visit the Multi-drug-resistant tuberculosis page.)

Neisseria gonorrhoeae[edit]

Neisseria gonorrhoeae is a sexually-transmitted pathogen that can cause pelvic pain, pain on urination, penile, and vaginal discharge, as well as systemic symptoms in human infection. The bacteria was first identified in 1879,[109] although some Biblical scholars believe that references to the disease can be found as early as Parshat Metzora of the Old Testament.[110]

Treatment with penicillin in the 1940s proved helpful, but by the 1970s resistant strains predominated. Resistance to penicillin has developed through two mechanisms: chomasomally mediated resistance (CMRNG) and penicillinase-mediated resistance (PPNG). CMRNG involves stepwise mutation of penA, which codes for the penicilin-binding protein (PBP-2); mtr, which encodes an efflux pump to remove penicilin from the cell; and penB, which encodes the bacterial cell wall porins. PPNG involves the acquisition of a plasmid-borne beta-lactamase.[111] Fluoroquinolones were a useful next-line treatment until resistance was achieved through efflux pumps and mutations to the gyrA gene, which encodes DNA gyrase.[111] Third-generation cephalosporins have been used to treat gonorrhoea since 2007, although resistant strains have emerged. Strains of Neisseria gonorrhoea have also been found to be resistant to tetracyclines and aminoglycosides. Neisseria gonorrheoea has a high affinity for horizontal gene transfer, and as a result, the existence of any strain resistant to a given drug could spread easily across strains. Today, injectable ceftriaxone is used, sometimes in combination with azithromycin or doxycycline.[112][113]

Alternatives[edit]

Prevention[edit]

Rational use of antibiotics may reduce the chances of development of opportunistic infection by antibiotic-resistant bacteria due to dysbacteriosis. Our immune systems will cure minor bacterial infections on their own. If we give it the chance without relying on antibiotics to cure a small infection, it will be less likely to become immune or resistant to the antibiotic. It is also important to note that antibiotics will not cure viral infections. Taking an antibiotic unnecessarily to treat a viral infection can lead to the resistance of antibiotics[114] In one study, the use of fluoroquinolones is clearly associated with Clostridium difficile infection, which is a leading cause of nosocomial diarrhea in the United States,[115] and a major cause of death, worldwide.[116]

Vaccines do not have the problem of resistance because a vaccine enhances the body's natural defenses, whereas an antibiotic operates separately from the body's normal defenses. Nevertheless, new strains that escape immunity induced by vaccines may evolve; for example, an updated influenza vaccine is needed each year.

While theoretically promising, antistaphylococcal vaccines have shown limited efficacy, because of immunological variation between Staphylococcus species, and the limited duration of effectiveness of the antibodies produced. Development and testing of more effective vaccines is underway.[117]

The Australian Commonwealth Scientific and Industrial Research Organization (CSIRO), realizing the need for the reduction of antibiotic use, has been working on two alternatives. One alternative is to prevent diseases by adding cytokines instead of antibiotics to animal feed.[118] These proteins are made in the animal body "naturally" after a disease and are not antibiotics, so they do not contribute to the problem of antibiotic resistance. Furthermore, studies on using cytokines have shown they also enhance the growth of animals like the antibiotics now used, but without the drawbacks of nontherapeutic antibiotic use. Cytokines have the potential to achieve the animal growth rates traditionally sought by the use of antibiotics without the contribution of antibiotic resistance associated with the widespread nontherapeutic uses of antibiotics currently used in the food animal production industries. In addition, CSIRO is working on vaccines for diseases.[118]

Phage therapy[edit]

Phage therapy, an approach that has been extensively researched and used as a therapeutic agent for over 60 years, especially in the Soviet Union, represents a potentially significant but currently underdeveloped approach to the treatment of bacterial disease.[119] Phage therapy was widely used in the United States until the discovery of antibiotics, in the early 1940s. Bacteriophages or "phages" are viruses that invade bacterial cells and, in the case of lytic phages, disrupt bacterial metabolism and cause the bacterium to lyse. Phage therapy is the therapeutic use of lytic bacteriophages to treat pathogenic bacterial infections.[120] [121] [122]

Bacteriophage therapy is an important alternative to antibiotics in the current era of multidrug-resistant pathogens. A review of studies that dealt with the therapeutic use of phages from 1966 to 1996 and few latest ongoing phage therapy projects via internet showed: Phages were used topically, orally or systemically in Polish and Soviet studies. The success rate found in these studies was 80–95%, with few gastrointestinal or allergic side-effects. British studies also demonstrated significant efficacy of phages against Escherichia coli, Acinetobacter spp., Pseudomonas spp., and Staphylococcus aureus. US studies dealt with improving the bioavailability of phage. Phage therapy may prove as an important alternative to antibiotics for treating multidrug-resistant pathogens.[123]

Discovery of the structure of the viral protein PlyC is allowing researchers to understand the way it kills a significant range of pathogenic bacteria.[124]

Research[edit]

Development pipeline[edit]

Since the discovery of antibiotics, research and development (R&D) efforts have provided new drugs in time to treat bacteria that became resistant to older antibiotics, but in the 2000s there has been concern that development has slowed enough that seriously ill patients may run out of treatment options.[125] Another concern is that doctors may become reluctant to perform routine surgeries due to the increased risk of harmful infection.[126] Backup treatments can have serious side-effects; for example, treatment of multi-drug-resistant tuberculosis can cause deafness and insanity.[127] The potential crisis at hand is the result of a marked decrease in industry R&D.[128] Poor financial investment in antibiotic research has exacerbated the situation.[128] In 2011, Pfizer, one of the last major pharmaceutical companies developing new antibiotics, shut down its primary research effort, citing poor shareholder returns relative to drugs for chronic illnesses.[129]

In the United States, drug companies and the administration of President Barack Obama have been proposing changing the standards by which the FDA approves antibiotics targeted at resistant organisms.[126][130] On 12 December 2013, the Antibiotic Development to Advance Patient Treatment (ADAPT) Act of 2013 was introduced in the U.S. Congress. The ADAPT Act aims to fast-track the drug development in order to combat the growing public health threat of 'superbugs'. Under this Act, FDA can approve antibiotics and antifungals needed for life-threatening infections based on data from smaller clinical trial. The CDC will reinforce the monitoring of the use of antibiotics that treat serious and life-threatening infections and the emerging resistance, and make the data publicly available. The FDA antibiotics labeling process, 'Susceptibility Test Interpretive Criteria for Microbial Organisms' or 'breakpoints' is also streamlined to allow the most up-to-date and cutting-edge data available to healthcare professionals under the new Act.[131][132]

The U.S. National Institutes of Health plans to fund a new research network on the issue up to $62 million from 2013 to 2019.[133] Using authority created by the Pandemic and All Hazards Preparedness Act of 2006, the Biomedical Advanced Research and Development Authority in the U.S. Department of Health and Human Services announced that it will spend between $40 million and $200 million in funding for R&D on new antibiotic drugs under development by GlaxoSmithKline.[134]

Mechanism[edit]

In research published on October 17, 2008 in Cell, a team of scientists pinpointed the place on bacteria where the antibiotic myxopyronin launches its attack, and why that attack is successful. The myxopyronin binds to and inhibits the crucial bacterial enzyme RNA polymerase. The myxopyronin changes the structure of the switch-2 segment of the enzyme, inhibiting its function of reading and transmitting DNA code. This prevents RNA polymerase from delivering genetic information to the ribosomes, causing the bacteria to die.[135]

In 2012, a team of the University of Leipzig modified a peptide found in honeybees. It is effective against 37 types of bacteria.[136]

One major cause of antibiotic resistance is the increased pumping activity of microbial ABC transporters, which diminishes the effective drug concentration inside the microbial cell. ABC transporter inhibitors that can be used in combination with current antimicrobials are being tested in clinical trials and are available for therapeutic regimens.[137]

Applications[edit]

Antibiotic resistance is an important tool for genetic engineering. By constructing a plasmid that contains an antibiotic-resistance gene as well as the gene being engineered or expressed, a researcher can ensure that, when bacteria replicate, only the copies that carry the plasmid survive. This ensures that the gene being manipulated passes along when the bacteria replicates.

In general, the most commonly used antibiotics in genetic engineering are "older" antibiotics that have largely fallen out of use in clinical practice. These include:

In industry, the use of antibiotic resistance is disfavored, since maintaining bacterial cultures would require feeding them large quantities of antibiotics. Instead, the use of auxotrophic bacterial strains (and function-replacement plasmids) is preferred.

See also[edit]

Footnotes[edit]

  1. ^ name=cdcgetsmart>"Antibiotic Resistance Questions & Answers". Get Smart: Know When Antibiotics Work. Centers for Disease Control and Prevention, USA. 30 June 2009. Retrieved 20 March 2013. 
  2. ^ a b Zainuddin, ZF; Dale, JW (1990). "Does Mycobacterium tuberculosis have plasmids?". Tubercle 71 (1): 43–9. PMID 2115217. 
  3. ^ Louw, G. E.; Warren, R. M.; Gey Van Pittius, N. C.; McEvoy, C. R. E.; Van Helden, P. D.; Victor, T. C. (2009). "A Balancing Act: Efflux/Influx in Mycobacterial Drug Resistance". Antimicrobial Agents and Chemotherapy 53 (8): 3181–9. doi:10.1128/AAC.01577-08. PMC 2715638. PMID 19451293. 
  4. ^ D'Costa et al. 2011, pp. 457–461.
  5. ^ Donadio et al. 2010, pp. 423–430.
  6. ^ Caldwell & Lindberg 2011.
  7. ^ Nelson 2009, p. 294.
  8. ^ Hawkey & Jones 2009, pp. i3-i10.
  9. ^ WHO (January 2002). "Use of antimicrobials outside human medicine and resultant antimicrobial resistance in humans". World Health Organization. Archived from the original on 13 May 2004. 
  10. ^ Ferber, Dan (4 January 2002). "Livestock Feed Ban Preserves Drugs' Power". Science 295 (5552): 27–28. doi:10.1126/science.295.5552.27a. PMID 11778017. 
  11. ^ a b Mathew, AG; Cissell, R; Liamthong, S (2007). "Antibiotic resistance in bacteria associated with food animals: a United States perspective of livestock production". Foodborne Pathog. Dis. 4 (2): 115–33. doi:10.1089/fpd.2006.0066. PMID 17600481. 
  12. ^ CDC. "Antibiotic Resistance Questions & Answers" [Are antibacterial-containing products (soaps, household cleaners, etc.) better for preventing the spread of infection? Does their use add to the problem of resistance?]. Atlanta, Georgia, USA.: Centers for Disease Control and Prevention. Archived from the original on 8 November 2009. Retrieved November 17, 2009. 
  13. ^ Larsson, DG.; Fick, J. (Jan 2009). "Transparency throughout the production chain -- a way to reduce pollution from the manufacturing of pharmaceuticals?". Regul Toxicol Pharmacol 53 (3): 161–3. doi:10.1016/j.yrtph.2009.01.008. PMID 19545507. 
  14. ^ Healthcare-associated Infections
  15. ^ "Antibiotic resistance". Sciencedaily.com. Retrieved 2013-06-12. 
  16. ^ Tacconelli, E; De Angelis, G; Cataldo, MA; Pozzi, E; Cauda, R (January 2008). "Does antibiotic exposure increase the risk of methicillin-resistant Staphylococcus aureus (MRSA) isolation? A systematic review and meta-analysis". J. Antimicrob. Chemother. 61 (1): 26–38. doi:10.1093/jac/dkm416. PMID 17986491. 
  17. ^ Muto, CA.; Jernigan, JA.; Ostrowsky, BE.; Richet, HM.; Jarvis, WR.; Boyce, JM.; Farr, BM. (May 2003). "SHEA guideline for preventing nosocomial transmission of multidrug-resistant strains of Staphylococcus aureus and enterococcus". Infect Control Hosp Epidemiol 24 (5): 362–86. doi:10.1086/502213. PMID 12785411. 
  18. ^ Vonberg, Dr Ralf-Peter. "Clostridium difficile: a challenge for hospitals". European Center for Disease Prevention and Control. Institute for Medical Microbiology and Hospital Epidemiology: IHE. Archived from the original on 11 June 2009. Retrieved 27 July 2009. 
  19. ^ Kuijper, EJ; van Dissel, J.; Wilcox, MH (Aug 2007). "Clostridium difficile: changing epidemiology and new treatment options". Current Opinion in Infectious Diseases 20 (4): 376–83. doi:10.1097/QCO.0b013e32818be71d. PMID 17609596. 
  20. ^ editors, Ronald Eccles, Olaf Weber, (2009). Common cold (Online-Ausg. ed.). Basel: Birkhäuser. p. 240. ISBN 978-3-7643-9894-1. 
  21. ^ a b c Wright, GD (October 2010). "Antibiotic resistance in the environment: a link to the clinic?". Current Opinion in Microbiology 13 (5): 589–94. doi:10.1016/j.mib.2010.08.005. PMID 20850375. 
  22. ^ "Mutations are random". University of California. Retrieved Aug 14, 2011. 
  23. ^ Richard William Nelson. Darwin, Then and Now: The Most Amazing Story in the History of Science, iUniverse, 2009, p. 294
  24. ^ Wayne W. Umbreit, Advances in Applied Microbiology, vol. 11, Academic Press, 1970, p. 80
  25. ^ M. R. Pollock. "Origin and Function of Penicillinase: a Problem in Biochemical Evolution",British Medical Journal, 14 Oct 1967, p. 76
  26. ^ a b New Scientist, Jun 8, 1972, p. 546
  27. ^ a b New Scientist, Feb 11, 1989, p. 34
  28. ^ Pollock, p. 77
  29. ^ Abigail A. Salyers, Dixie D. Whitt. Revenge of the microbes: how bacterial resistance is undermining the antibiotic miracle, ASM Press, 2005, p. 34
  30. ^ http://www.nobelprize.org/nobel_prizes/medicine/laureates/1945/fleming-lecture.pdf
  31. ^ Arnold, SR; Straus, SE (2005). "Interventions to improve antibiotic prescribing practices in ambulatory care". In Arnold, Sandra R. Cochrane Database of Systematic Reviews (4): CD003539. doi:10.1002/14651858.CD003539.pub2. PMID 16235325. 
  32. ^ McNulty, CA; Boyle, P; Nichols, T; Clappison, P; Davey, P (August 2007). "The public's attitudes to and compliance with antibiotics". J. Antimicrob. Chemother. 60 Suppl 1: i63–8. doi:10.1093/jac/dkm161. PMID 17656386. 
  33. ^ editors, Ronald Eccles, Olaf Weber, (2009). Common cold (Online-Ausg. ed.). Basel: Birkhäuser. p. 234. ISBN 978-3-7643-9894-1. 
  34. ^ Pechère, JC (September 2001). "Patients' interviews and misuse of antibiotics". Clin. Infect. Dis. 33 Suppl 3: S170–3. doi:10.1086/321844. PMID 11524715. 
  35. ^ Costelloe, Ceire; Metcalfe, Chris; Lovering, Andrew; Mant, David; Hay, Alastair D (May 2010). "Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: systematic review and meta-analysis". BMJ (BMJ) 340: c2096. doi:10.1136/bmj.c2096. 
  36. ^ Li, JZ; Winston, LG; Moore, DH; Bent, S (September 2007). "Efficacy of short-course antibiotic regimens for community-acquired pneumonia: a meta-analysis". Am. J. Med. 120 (9): 783–90. doi:10.1016/j.amjmed.2007.04.023. PMID 17765048. 
  37. ^ Bignardi, G.E. (31 August 1998). "Risk factors for Clostridium difficile infection". Journal of Hospital Infection 40 (1): 1–15. doi:10.1016/S0195-6701(98)90019-6. PMID 9777516. 
  38. ^ Runyon, BA; McHutchison, JG; Antillon, MR; Akriviadis, EA; Montano, AA (June 1991). "Short-course versus long-course antibiotic treatment of spontaneous bacterial peritonitis. A randomized controlled study of 100 patients". Gastroenterology 100 (6): 1737–42. PMID 2019378. 
  39. ^ Singh, Nina; PAUL ROGERS, CHARLES W. ATWOOD, MARILYN M. WAGENER and VICTOR L. YU (1 August 2000). "Short-course Empiric Antibiotic Therapy for Patients with Pulmonary Infiltrates in the Intensive Care Unit A Proposed Solution for Indiscriminate Antibiotic Prescription". Am. J. Respir. Crit. Care Med. 162 (2): 505–511. doi:10.1164/ajrccm.162.2.9909095. PMID 10934078. 
  40. ^ Gleisner, Ana L.M; Argenta, Rodrigo; Pimentel, Marcelo; Simon, Tatiana K; Jungblut, Carlos F; Petteffi, Leonardo; de Souza, Rafael M; Sauerssig, Mauricio; Kruel, Cleber D.P; Machado, Adão R.L (30 April 2004). "Infective complications according to duration of antibiotic treatment in acute abdomen". International Journal of Infectious Diseases 8 (3): 155–162. doi:10.1016/j.ijid.2003.06.003. PMID 15109590. 
  41. ^ Pichichero, Michael E.; Cohen, Robert (1997). "Shortened course of antibiotic therapy for acute otitis media, sinusitis and tonsillopharyngitis". The Pediatric Infectious Disease Journal 16 (7): 680–95. doi:10.1097/00006454-199707000-00011. PMID 9239773. 
  42. ^ Dellinger, E. Patchen; Wertz, MJ; Lennard, ES; Oreskovich, MR (1986). "Efficacy of Short-Course Antibiotic Prophylaxis After Penetrating Intestinal Injury". Archives of Surgery 121 (1): 23–30. doi:10.1001/archsurg.1986.01400010029002. PMID 3942496. 
  43. ^ Perez-Gorricho, B; Ripoll, M; Pace Study, Group (2003). "Does short-course antibiotic therapy better meet patient expectations?". International Journal of Antimicrobial Agents 21 (3): 222–8. doi:10.1016/S0924-8579(02)00360-6. PMID 12636982. 
  44. ^ Keren, R.; Chan, E. (2002). "A Meta-analysis of Randomized, Controlled Trials Comparing Short- and Long-Course Antibiotic Therapy for Urinary Tract Infections in Children". Pediatrics 109 (5): E70–0. doi:10.1542/peds.109.5.e70. PMID 11986476. 
  45. ^ Casey, JR; Pichichero, ME (2005). "Metaanalysis of short course antibiotic treatment for group a streptococcal tonsillopharyngitis". The Pediatric infectious disease journal 24 (10): 909–17. PMID 16220091. 
  46. ^ McCormack, J.; Allan, G. M. (2012). "A prescription for improving antibiotic prescribing in primary care". BMJ 344: d7955. doi:10.1136/bmj.d7955. PMID 22302779. 
  47. ^ "Should you stop an antibiotic course early?" (PDF). Retrieved 2013-03-12. 
  48. ^ Marc Bonten, MD; Eijkman-Winkler Institute for Medical Microbiology, Infectious Diseases, and Inflammation; Utrecht, the Netherland | http://hicsigwiki.asid.net.au/images/4/41/Should_you_stop_an_antibiotic_course_early_if_you_feel_better_R._Everts.pdf
  49. ^ Pechère, JC; Hughes, D; Kardas, P; Cornaglia, G (March 2007). "Non-compliance with antibiotic therapy for acute community infections: a global survey". Int. J. Antimicrob. Agents 29 (3): 245–53. doi:10.1016/j.ijantimicag.2006.09.026. PMID 17229552. 
  50. ^ Kardas, P (March 2007). "Comparison of patient compliance with once-daily and twice-daily antibiotic regimens in respiratory tract infections: results of a randomized trial". J. Antimicrob. Chemother. 59 (3): 531–6. doi:10.1093/jac/dkl528. PMID 17289766. 
  51. ^ Thomas, JK; Forrest, A; Bhavnani, SM; Hyatt, JM; Cheng, A; Ballow, CH; Schentag, JJ (March 1998). "Pharmacodynamic Evaluation of Factors Associated with the Development of Bacterial Resistance in Acutely Ill Patients during Therapy". Antimicrob. Agents Chemother. 42 (3): 521–7. PMC 105492. PMID 9517926. 
  52. ^ Girou, E; Legrand, P; Soing-Altrach, S; Lemire, Astrid; Poulain, Celine; Allaire, Alexandra; Tkoub‐Scheirlinck, Latifa; Chai, Steeve Ho Tam et al. (October 2006). "Association between hand hygiene compliance and methicillin-resistant Staphylococcus aureus prevalence in a French rehabilitation hospital". Infect Control Hosp Epidemiol 27 (10): 1128–30. doi:10.1086/507967. PMID 17006822. 
  53. ^ Swoboda, SM; Earsing, K; Strauss, K; Lane, S; Lipsett, PA (February 2004). "Electronic monitoring and voice prompts improve hand hygiene and decrease nosocomial infections in an intermediate care unit". Crit. Care Med. 32 (2): 358–63. doi:10.1097/01.CCM.0000108866.48795.0F. PMID 14758148. 
  54. ^ Farmer, Paul E., Bruce Nizeye, Sara Stulac, and Salmaan Keshavjee. 2006. Structural Violence and Clinical Medicine. PLoS Medicine, 1686–1691.
  55. ^ The Resistance Phenomenon in Microbes and Infectious Disease Vectors: Implications for Human Health and Strategies for Containment: Workshop Summary. Institute of Medicine (US) Forum on Emerging Infections; Knobler SL, Lemon SM, Najafi M, et al., editors. Washington (DC): National Academies Press (US); 2003.[1]
  56. ^ Hersom, Matt. "Application of Ionophores in Cattle Diets". AN285 Department of Animal Sciences. University of Florida IFAS Extension. Retrieved 14 March 2013. 
  57. ^ Schneider, K; Garrett, L (June 19, 2009). "Non-therapeutic Use of Antibiotics in Animal Agriculture, Corresponding Resistance Rates, and What Can be Done About It". Center for Global Development. 
  58. ^ Hurd HS, Doores S, Hayes D, Mathew A, Maurer J, Silley P, Singer RS, Jones RN. “Public health consequences of macrolide use in food animals: a deterministic risk assessment “. J Food Prot. 2004 May;67(5):980-92
  59. ^ Hurd HS, Malladi S. “A stochastic assessment of the public health risks of the use of macrolide antibiotics in food animals”. Risk Anal. 2008 Jun;28(3):695-710. doi: 10.1111/j.1539-6924.2008.01054.x
  60. ^ Joint FAO/OIE/WHO Expert Workshop on Non-Human Antimicrobial Usage and Antimicrobial Resistance: Scientific assessment [2]
  61. ^ OIE,Terrestrial Animal Health Code
  62. ^ OIE,Terrestrial Animal Health Code
  63. ^ OIE,Terrestrial Animal Health Code
  64. ^ Castanon, J.I. (2007). "History of the use of antibiotic as growth promoters in European poultry feeds". Poult. Sci. 86 (11): 2466–71. doi:10.3382/ps.2007-00249. PMID 17954599. 
  65. ^ Bengtsson, B.; Wierup, M. (2006). "Antimicrobial resistance in Scandinavia after ban of antimicrobial growth promoters". Anim. Biotechnol. 17 (2): 147–56. doi:10.1080/10495390600956920. PMID 17127526. 
  66. ^ "GAO-11-801, Antibiotic Resistance: Agencies Have Made Limited Progress Addressing Antibiotic Use in Animals". gao.gov. Retrieved 2014-01-25. 
  67. ^ Sapkota, AR; Lefferts, LY; McKenzie, S; Walker, P (May 2007). "What Do We Feed to Food-Production Animals? A Review of Animal Feed Ingredients and Their Potential Impacts on Human Health". Environ. Health Perspect. 115 (5): 663–70. doi:10.1289/ehp.9760. PMC 1867957. PMID 17520050. 
  68. ^ Baker, R (2006). "Health management with reduced antibiotic use — the U.S. experience". Anim. Biotechnol. 17 (2): 195–205. doi:10.1080/10495390600962274. PMID 17127530. 
  69. ^ "Executive summary from the UCS report "Hogging It: Estimates of Antimicrobial Abuse in Livestock"". Union of Concerned Scientists. January 2001. 
  70. ^ Nelson, JM.; Chiller, TM.; Powers, JH.; Angulo, FJ. (Apr 2007). "Fluoroquinolone-resistant Campylobacter species and the withdrawal of fluoroquinolones from use in poultry: a public health success story". Clin Infect Dis 44 (7): 977–80. doi:10.1086/512369. PMID 17342653. 
  71. ^ APHIS. "Clostridium difficile on U.S. Swine Operations". Retrieved 24 October 2013. 
  72. ^ "US Senate Bill S. 549: Preservation of Antibiotics for Medical Treatment Act of 2007". 
  73. ^ US House Bill H.R. 962: "Preservation of Antibiotics for Medical Treatment Act of 2007". 
  74. ^ John Gever (March 23, 2012). "FDA Told to Move on Antibiotic Use in Livestock". MedPage Today. Retrieved March 24, 2012. 
  75. ^ Gardiner Harris (April 11, 2012). "U.S. Tightens Rules on Antibiotics Use for Livestock". The New York Times. Retrieved April 12, 2012. 
  76. ^ "FDA's Strategy on Antimicrobial Resistance — Questions and Answers". U.S. Food and Drug Administration. April 11, 2012. Retrieved April 12, 2012. "“Judicious use” is using an antimicrobial drug appropriately and only when necessary; Based on a thorough review of the available scientific information, FDA recommends that use of medically important antimicrobial drugs in food-producing animals be limited to situations where the use of these drugs is necessary for ensuring animal health, and their use includes veterinary oversight or consultation. FDA believes that using medically important antimicrobial drugs to increase production in food-producing animals is not a judicious use." 
  77. ^ Tavernise, Sabrina. "F.D.A. to Phase Out Use of Some Antibiotics in Animals Raised for Meat". The New York Times. Retrieved 11 December 2013. 
  78. ^ a b Martinez, J. L., & Olivares, J. (2012). Envrironmental Pollution By Antibiotic Resistance Genes. In P. L. Keen, & M. H. Montforts, Antimicrobial Resistance in the Environment (pp. 151- 171). Hoboken, N.J.: John Wiley & Sons.
  79. ^ Pruden, A., & Arabi, M. (2012). Quantifying Anthropogenic Impacts on Environmental Reservoirs of Antibiotic Resistance. In P. L. Keen, & M. H. Montforts, Antimicrobial Resistance in the Environment (pp. 173-202). Hoboken, N.J.: John Wiley & Sons.
  80. ^ Ochiai, K.; Yamanaka, T; Kimura, K; Sawada, O (1959). "Inheritance of drug resistance (and its transfer) between Shigella strains and Between Shigella and E.coli strains". Hihon Iji Shimpor, (in Japanese) 34: 1861. 
  81. ^ Li, X; Nikadio, H (2009). "Efflux-Mediated Drug Resistance in Bacteria: an Update". Drug 69 (12): 1555–623. doi:10.2165/11317030-000000000-00000. PMC 2847397. PMID 19678712. 
  82. ^ Morita, Y; Kodama, K; Shiota, S; Mine, T; Kataoka, A; Mizushima, T; Tsuchiya, T (July 1998). "NorM, a Putative Multidrug Efflux Protein, of Vibrio parahaemolyticus and Its Homolog in Escherichia coli". Antimicrob. Agents Chemother. 42 (7): 1778–82. PMC 105682. PMID 9661020. 
  83. ^ Robicsek, A; Jacoby, GA; Hooper, DC (October 2006). "The worldwide emergence of plasmid-mediated quinolone resistance". Lancet Infect Dis 6 (10): 629–40. doi:10.1016/S1473-3099(06)70599-0. PMID 17008172. 
  84. ^ Cirz, RT; Chin, JK; Andes, DR; de Crécy-Lagard, V; Craig, WA; Romesberg, FE (2005). "Inhibition of Mutation and Combating the Evolution of Antibiotic Resistance". PLoS Biol. 3 (6): e176. doi:10.1371/journal.pbio.0030176. PMC 1088971. PMID 15869329. 
  85. ^ Chan, CX; Beiko, RG; Ragan, MA (August 2011). "Lateral Transfer of Genes and Gene Fragments in Staphylococcus Extends beyond Mobile Elements". J Bacteriol 193 (15): 3964–3977. doi:10.1128/JB.01524-10. PMC 3147504. PMID 21622749. 
  86. ^ "CDC: Get Smart: Know When Antibiotics Work". Cdc.gov. Retrieved 2013-06-12. 
  87. ^ "APUA: General Background: Antibiotic Resistance, A Societal Problem". Tufts.edu. Retrieved 2013-06-12. 
  88. ^ Bozdogan, B. Ü.; Esel, D.; Whitener, C.; Browne, F. A.; Appelbaum, P. C. (2003). "Antibacterial susceptibility of a vancomycin-resistant Staphylococcus aureus strain isolated at the Hershey Medical Center". Journal of Antimicrobial Chemotherapy 52 (5): 864–868. doi:10.1093/jac/dkg457. PMID 14563898.  edit
  89. ^ Xie et al.; Pierce, Joshua G.; James, Robert C.; Okano, Akinori; Boger, Dale L. (2011). "A Redesigned Vancomycin Engineered for Dual d-Ala-d-Ala and d-Ala-d-Lac Binding Exhibits Potent Antimicrobial Activity Against Vancomycin-Resistant Bacteria". J. Am. Chem. Soc. 133, 133 (35): 13946–9. doi:10.1021/ja207142h. PMC 3164945. PMID 21823662. 
  90. ^ Tsiodras, Sotirios; Gold, Howard S; Sakoulas, George; Eliopoulos, George M; Wennersten, Christine; Venkataraman, Lata; Moellering, Robert C; Ferraro, Mary Jane. "Linezolid resistance in a clinical isolate of Staphylococcus aureus". The Lancet 358 (9277): 207–208. doi:10.1016/S0140-6736(01)05410-1. PMID 11476839. 
  91. ^ Boyle-Vavra, S; Daum, RS (2007). "Community-acquired methicillin-resistant Staphylococcus aureus: the role of Panton-Valentine leukocidin". Lab. Invest. 87 (1): 3–9. doi:10.1038/labinvest.3700501. PMID 17146447. 
  92. ^ Maree, CL; Daum, RS; Boyle-Vavra, S; Matayoshi, K; Miller, LG (2007). "Community-associated Methicillin-resistant Staphylococcus aureus Isolates and Healthcare-Associated Infections". Emerging Infect. Dis. 13 (2): 236–42. doi:10.3201/eid1302.060781. PMC 2725868. PMID 17479885. 
  93. ^ CDCP (2005-10-11). "Group A Streptococcal (GAS) Disease (strep throat, necrotizing fasciitis, impetigo) -- Frequently Asked Questions". Centers for Disease Control and Prevention. Archived from the original on 19 December 2007. Retrieved 2007-12-11. 
  94. ^ a b Albrich, W; Monnet, DL; Harbarth, S (2004). "Antibiotic selection pressure and resistance in Streptococcus pneumoniae and Streptococcus pyogenes". Emerging Infect. Dis. 10 (3): 514–7. doi:10.3201/eid1003.030252. PMC 3322805. PMID 15109426. 
  95. ^ Hidron, AI; Edwards, JR; Patel, J; Horan, Teresa C.; Sievert, Dawn M.; Pollock, Daniel A.; Fridkin, Scott K.; National Healthcare Safety Network Team; Participating National Healthcare Safety Network Facilities (November 2008). "NHSN annual update: antimicrobial-resistant pathogens associated with healthcare-associated infections: annual summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2006-2007". Infect Control Hosp Epidemiol 29 (11): 996–1011. doi:10.1086/591861. PMID 18947320. 
  96. ^ Poole,, K. (2004). "Efflux-mediated multiresistance in Gram-negative bacteria". Clinical Microbiology and Infection 10 (1): 12–26. doi:10.1111/j.1469-0691.2004.00763.x. PMID 14706082. 
  97. ^ Nguyen, D.; Joshi-Datar, A.; Lepine, F.; Bauerle, E.; Olakanmi, O.; Beer, K.; McKay, G.; Siehnel, R.; Schafhauser, J.; Wang, Y.; Britigan, B. E.; Singh, P. K. (2011). "Active Starvation Responses Mediate Antibiotic Tolerance in Biofilms and Nutrient-Limited Bacteria". Science 334 (6058): 982–6. doi:10.1126/science.1211037. PMID 22096200. 
  98. ^ Gerding, D.N.; Johnson, S.; Peterson, L.R.; Mulligan, M.E.; Silva, J. Jr. (1995). "Clostridium difficile-associated diarrhea and colitis". Infect. Control. Hosp. Epidemiol. 16 (8): 459–477. doi:10.1086/648363. PMID 7594392. 
  99. ^ McDonald, L (2005). "Clostridium difficile: responding to a new threat from an old enemy". Infect. Control. Hosp. Epidemiol. 26 (8): 672–5. doi:10.1086/502600. PMID 16156321. 
  100. ^ Johnson, S.; Samore, M.H.; Farrow, K.A; Killgore, George E.; Tenover, Fred C.; Lyras, Dena; Rood, Julian I.; Degirolami, Paola et al. (1999). "Epidemics of diarrhea caused by a clindamycin-resistant strain of Clostridium difficile in four hospitals". New England Journal of Medicine 341 (23): 1645–1651. doi:10.1056/NEJM199911253412203. PMID 10572152. 
  101. ^ Loo, V; Poirier, L; Miller, M; Oughton, Matthew; Libman, Michael D.; Michaud, Sophie; Bourgault, Anne-Marie; Nguyen, Tuyen et al. (2005). "A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality". N Engl J Med 353 (23): 2442–9. doi:10.1056/NEJMoa051639. PMID 16322602. 
  102. ^ Centers for Disease Control and Prevention (CDC) (2004). "Acinetobacter baumannii infections among patients at military medical facilities treating injured U.S. service members, 2002-2004". MMWR Morb. Mortal. Wkly. Rep. (Centers for Disease Control and Prevention (CDC)) 53 (45): 1063–6. PMID 15549020. 
  103. ^ "Medscape abstract on Acinetobacter baumannii: Acinetobacter baumannii: An Emerging Multidrug-resistant Threat". "membership only website" 
  104. ^ Arnold, Ryan S.; Thom, Kerri A.; Sharma, Saarika; Phillips, Michael; Kristie Johnson, J.; Morgan, Daniel J. (2011). "Emergence of Klebsiella pneumoniae Carbapenemase-Producing Bacteria". Southern Medical Journal 104 (1): 40–5. doi:10.1097/SMJ.0b013e3181fd7d5a. PMC 3075864. PMID 21119555. 
  105. ^ "Antimicrobial Resistance Still Poses a Public Health Threat: A Conversation With Edward J. Septimus, MD, FIDSA, FACP, FSHEA, Clinical Professor of Internal Medicine at Texas A&M Health Science Center". Agency for Healthcare Research and Quality. 2013-04-17. Retrieved 2013-09-26. 
  106. ^ a b Lobue, Philip (2009). "Extensively drug-resistant tuberculosis". Current Opinion in Infectious Diseases 22 (2): 167–73. doi:10.1097/QCO.0b013e3283229fab. PMID 19283912. 
  107. ^ Herzog, Basel (1998). "History of Tuberculosis". Respiration 65 (1): 5–15. doi:10.1159/000029220. PMID 9523361. 
  108. ^ Gao, Qian; Li, Xia (2010). "Transmission of MDR tuberculosis". Drug Discovery Today: Disease Mechanisms 7: e61. doi:10.1016/j.ddmec.2010.09.006. 
  109. ^ Ligon, B. Lee (October 2005). "Albert Ludwig Sigesmund Neisser: Discoverer of the Cause of Gonorrhea". Seminars in Pediatric Infectious Diseases 16 (4): 336–341. 
  110. ^ Rosner, Fred (1995). Medicine in the Bible and the Talmud : selections from classical Jewish sources (Augm. ed. ed.). Hoboken, NJ: KTAV Pub. House. ISBN 0-88125-506-8. 
  111. ^ a b Tapsall (2001) Antimicrobial resistance in Niesseria gonorrhoeae. World Health Organization.
  112. ^ Deguchi T, Nakane K, Yasuda M, Maeda S (September 2010). "Emergence and spread of drug resistant Neisseria gonorrhoeae". J. Urol. 184 (3): 851–8; quiz 1235. doi:10.1016/j.juro.2010.04.078. PMID 20643433. 
  113. ^ Centers for Disease Control and Prevention, (CDC) (Aug 10, 2012). "Update to CDC's Sexually Transmitted Diseases Treatment Guidelines, 2010: Oral Cephalosporins No Longer a Recommended Treatment for Gonococcal Infections.". MMWR. Morbidity and mortality weekly report 61 (31): 590–4. PMID 22874837. 
  114. ^ "Evolution of Antibiotic Resistance". PBS.org. WGBH Educational Foundation and Clear Blue Sky Productions, Inc. Retrieved 11 June 2013. 
  115. ^ McCusker, ME; Harris, AD; Perencevich, E; Roghmann, MC (2003). "Fluoroquinolone Use and Clostridium difficile–Associated Diarrhea". Emerging Infect. Dis. 9 (6): 730–3. doi:10.3201/eid0906.020385. PMC 3000134. PMID 12781017. 
  116. ^ Frost, F; Craun, GF; Calderon, RL (1998). "Increasing hospitalization and death possibly due to Clostridium difficile diarrheal disease". Emerging Infect. Dis. 4 (4): 619–25. doi:10.3201/eid0404.980412. PMC 2640242. PMID 9866738. 
  117. ^ "Immunity, Infectious Diseases,and Pandemics—What You Can Do". HomesteadSchools.com. Retrieved 2013-06-12. 
  118. ^ a b "Science,Technology,genetics,research on biotechnology: December 2009". Biotechnolo.blogspot.com. Retrieved 2013-06-12. 
  119. ^ Keen, E. C. (2012). "Phage Therapy: Concept to Cure". Frontiers in Microbiology 3. doi:10.3389/fmicb.2012.00238.  edit
  120. ^ Chanishvili, N; Chanishvili, T; Tediashvili, M.; Barrow, P.A. (2001). "Phages and their application against drug-resistant bacteria". J. Chem. Technol. Biotechnol. 76 (7): 689–699. doi:10.1002/jctb.438. 
  121. ^ Jikia, D.; Chkhaidze, N.; Imedashvili, E.; Mgaloblishvili, I.; Tsitlanadze, G.; Katsarava, R.; Glenn Morris, J.; Sulakvelidze, Alexander (2005). "The use of a novel biodegradable preparation capable of the sustained release of bacteriophages and ciprofloxacin, in the complex treatment of multidrug-resistant Staphylococcus aureus-infected local radiation injuries caused by exposure to Sr90". Clinical & Experimental Dermatology 30 (1): 23–6. doi:10.1111/j.1365-2230.2004.01600.x. PMID 15663496. 
  122. ^ Weber-Dabrowska, B; Mulczyk, M; Górski, A (June 2003). "Bacteriophages as an efficient therapy for antibiotic-resistant septicemia in man". Transplant. Proc. 35 (4): 1385–6. doi:10.1016/S0041-1345(03)00525-6. PMID 12826166. 
  123. ^ Mathur, MD; Vidhani, S; Mehndiratta, PL; Bhalla, P; Reddy, B S N (2003). "Bacteriophage therapy: an alternative to conventional antibiotics". J Assoc Physicians India 51 (8): 593–6. doi:10.1258/095646202760159701. PMID 12194741. 
  124. ^ Scientists discover possible antibiotics alternative - Australian Broadcasting Corporation — Retrieved 29 July 2012.
  125. ^ CMO Annual Report
  126. ^ a b Obama Administration Seeks To Ease Approvals For Antibiotics : Shots - Health News : NPR
  127. ^ Moldova Grapples With Whether To Isolate TB Patients : NPR
  128. ^ a b Walsh, Fergus. "BBC News — Antibiotics resistance 'as big a risk as terrorism' - medical chief". Bbc.co.uk. Retrieved 2013-03-12. 
  129. ^ Gever, John (2011-02-04). "Pfizer Moves May Dim Prospect for New Antibiotics". MedPage Today. Retrieved 2013-03-12. 
  130. ^ Ledford, Heidi (2012). "FDA under pressure to relax drug rules". Nature 492 (7427): 19. doi:10.1038/492019a. PMID 23222585. 
  131. ^ Press Release (12 December 2013). "Green, Gingrey Introduce ADAPT Act to Safeguard Public Health". U.S. Congress. 
  132. ^ "Antibiotic Development to Advance Patient Treatment Act of 2013". U.S. Congress. 12 December 2013. 
  133. ^ NIH to fund clinical research network on antibacterial resistance
  134. ^ PHE
  135. ^ Mukhopadhyay, J.; Das, K.; Ismail, S.; Koppstein, D.; Jang, M.; Hudson, B.; Sarafianos, S.; Tuske, S.; Patel, J., Jansen, R., Irschik, H., Arnold, E., Ebright, R.H. (2008). "The RNA polymerase "switch region" is a target for inhibitors". Cell 135 (2): 295–307. doi:10.1016/j.cell.2008.09.033. PMC 2580802. PMID 18957204. 
  136. ^ "Modified Bee Peptide Slays Deadly Bacteria | Chemical & Engineering News". Cen.acs.org. 2012-05-29. Retrieved 2013-03-12. 
  137. ^ Ponte-Sucre, A, ed. (2009). ABC Transporters in Microorganisms. Caister Academic Press. ISBN 978-1-904455-49-3. [page needed]

References[edit]

Books
  • Caldwell, Roy; Lindberg, David, eds. (2011). "Understanding Evolution" [Mutations are random]. University of California Museum of Paleontology. Retrieved Aug 14, 2011. 
  • Nelson, Richard William (2009). Darwin, Then and Now: The Most Amazing Story in the History of Science (Self Published). iUniverse. p. 294. 
Journals

External links[edit]