Emerging infectious disease: Difference between revisions
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An '''emerging infectious disease''' ('''EID''') is an [[infectious disease]] whose incidence has increased recently (in the past 20 years), and could increase in the near future.<ref name=NIOSH>{{cite web |title=Emerging Infectious Diseases - NIOSH Workplace Safety and Health Topic |url=https://www.cdc.gov/niosh/topics/emerginfectdiseases/default.html |website=www.cdc.gov |publisher=[[Centers for Disease Control and Prevention]] |archiveurl=https://web.archive.org/web/20200418131812/https://www.cdc.gov/niosh/topics/emerginfectdiseases/default.html |archivedate=18 April 2020 |language=en-us |date=17 October 2018}}</ref> Such diseases do not respect national boundaries.<ref name=NIOSH/> The minority that are capable of developing [[Virulence|efficient transmission]] between humans can become major [[Public health|public]] and [[Global health|global]] concerns as potential causes of [[epidemic]]s or [[pandemic]]s.<ref name=Woolhouse2005/> Their many impacts can be [[economic]] and [[societal]], as well as clinical.<ref name=Morens2013>{{cite journal |vauthors=Morens DM, Fauci AS |authorlink2=Anthony Fauci |title=Emerging infectious diseases: threats to human health and global stability |journal=PLoS Pathogens |volume=9 |issue=7 |pages=e1003467 |date=2013 |pmid=23853589 |pmc=3701702 |doi=10.1371/journal.ppat.1003467}}</ref> |
An '''emerging infectious disease''' ('''EID''') is an [[infectious disease]] whose incidence has increased recently (in the past 20 years), and could increase in the near future.<ref name=NIOSH>{{cite web |title=Emerging Infectious Diseases - NIOSH Workplace Safety and Health Topic |url=https://www.cdc.gov/niosh/topics/emerginfectdiseases/default.html |website=www.cdc.gov |publisher=[[Centers for Disease Control and Prevention]] |archiveurl=https://web.archive.org/web/20200418131812/https://www.cdc.gov/niosh/topics/emerginfectdiseases/default.html |archivedate=18 April 2020 |language=en-us |date=17 October 2018}}</ref> Such diseases do not respect national boundaries.<ref name=NIOSH/> The minority that are capable of developing [[Virulence|efficient transmission]] between humans can become major [[Public health|public]] and [[Global health|global]] concerns as potential causes of [[epidemic]]s or [[pandemic]]s.<ref name=Woolhouse2005/> Their many impacts can be [[economic]] and [[societal]], as well as clinical.<ref name=Morens2013>{{cite journal |vauthors=Morens DM, Fauci AS |authorlink2=Anthony Fauci |title=Emerging infectious diseases: threats to human health and global stability |journal=PLoS Pathogens |volume=9 |issue=7 |pages=e1003467 |date=2013 |pmid=23853589 |pmc=3701702 |doi=10.1371/journal.ppat.1003467}}</ref> |
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Emerging infections account for at least 12% of all human [[pathogen]]s.<ref>{{cite journal | author = Taylor L. | year = 2001 | title = Risk factors for human disease emergence | url = | journal = Philosophical Transactions of the Royal Society B | volume = 356 | issue = 1411| pages = 983–9 | pmid = 11516376 | doi=10.1098/rstb.2001.0888 | pmc=1088493|display-authors=etal}}</ref> EIDs can be caused by newly identified [[microbe]]s, including [[Novel virus|novel]] species or strains of [[virus]]<ref>{{cite journal |author=Fauci AS |title=Emerging and reemerging infectious diseases: the perpetual challenge |journal=Academic Medicine|volume=80 |issue=12 |pages=1079–85 |year=2005 |pmid=16306276 |doi=10.1097/00001888-200512000-00002}}</ref> (e.g. [[novel coronavirus]]es, [[ebolavirus]]es, [[HIV]]). Some EIDs [[Evolution|evolve]] from a known pathogen, as occurs with new strains of [[influenza]]. EIDs may also result from spread of an existing disease to a new population in a different geographic region, as occurs with [[List of West Nile virus outbreaks|West Nile fever outbreaks]]. Some known diseases can also emerge in areas undergoing ecologic transformation (as in the case of [[Lyme disease]]<ref name=Kilpatrick2017>{{cite journal |vauthors=Kilpatrick AM, Dobson AD, Levi T, et al |title=Lyme disease ecology in a changing world: consensus, uncertainty and critical gaps for improving control |journal=Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences |volume=372 |issue=1722 |pages= |date=2017 |pmid=28438910 |pmc=5413869 |doi=10.1098/rstb.2016.0117 |url=}}</ref>). Others can experience a resurgence as a '''re-emerging infectious disease''', like [[tuberculosis]]<ref name=Porta2014>{{cite book |editors=Miquel Porta, Sander Greenland, Miguel Hernán, Isabel dos Santos Silva, John M. Last |title=A Dictionary of Epidemiology |page=92 |url=https://books.google.com/books?id=4kZmAwAAQBAJ |year=2014 |publisher=Oxford University Press |isbn=978-0-19-997673-7}}</ref> (following [[drug resistance]]) or [[measles]].<ref name=Fraser-bell2019>{{cite journal |last1=Fraser-bell |first1=C |title=Global Re-emergence of Measles - 2019 update |journal=Global Biosecurity |date=2019 |volume=1 |issue=3 |doi=10.31646/gbio.43 |url=https://www.jglobalbiosecurity.com/articles/10.31646/gbio.43/ |language=en |issn=2652-0036}}</ref> Nosocomial (hospital-acquired) infections, such as [[methicillin-resistant Staphylococcus aureus]] are emerging in hospitals, and are extremely problematic in that they are resistant to many antibiotics.<ref>{{cite journal |last1=Witte |first1=W |title=Increasing incidence and widespread dissemination of methicillin‐resistant Staphylococcus aureus (MRSA) in hospitals in central Europe, with special reference to German hospitals.|journal=Clinical Microbiology and Infection|date=1997|volume=3|issue=4|pages=414–22|doi=10.1111/j.1469-0691.1997.tb00277.x}}</ref> Of growing concern are adverse synergistic interactions between emerging diseases and other infectious and [[non-communicable diseases|non-infectious conditions]] leading to the development of novel [[syndemic]]s. |
Emerging infections account for at least 12% of all human [[pathogen]]s.<ref>{{cite journal | author = Taylor L. | year = 2001 | title = Risk factors for human disease emergence | url = | journal = Philosophical Transactions of the Royal Society B | volume = 356 | issue = 1411| pages = 983–9 | pmid = 11516376 | doi=10.1098/rstb.2001.0888 | pmc=1088493|display-authors=etal}}</ref> EIDs can be caused by newly identified [[microbe]]s, including [[Novel virus|novel]] species or strains of [[virus]]<ref>{{cite journal |author=Fauci AS |title=Emerging and reemerging infectious diseases: the perpetual challenge |journal=Academic Medicine|volume=80 |issue=12 |pages=1079–85 |year=2005 |pmid=16306276 |doi=10.1097/00001888-200512000-00002}}</ref> (e.g. [[novel coronavirus]]es, [[ebolavirus]]es, [[HIV]]). Some EIDs [[Evolution|evolve]] from a known pathogen, as occurs with new strains of [[influenza]]. EIDs may also result from spread of an existing disease to a new population in a different geographic region, as occurs with [[List of West Nile virus outbreaks|West Nile fever outbreaks]]. Some known diseases can also emerge in areas undergoing ecologic transformation (as in the case of [[Lyme disease]]<ref name=Kilpatrick2017>{{cite journal |vauthors=Kilpatrick AM, Dobson AD, Levi T, et al |title=Lyme disease ecology in a changing world: consensus, uncertainty and critical gaps for improving control |journal=Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences |volume=372 |issue=1722 |pages= |date=2017 |pmid=28438910 |pmc=5413869 |doi=10.1098/rstb.2016.0117 |url=}}</ref>). Others can experience a resurgence as a '''re-emerging infectious disease''', like [[tuberculosis]]<ref name=Porta2014>{{cite book |editors=Miquel Porta, Sander Greenland, [[Miguel Hernán]], Isabel dos Santos Silva, John M. Last |title=A Dictionary of Epidemiology |page=92 |url=https://books.google.com/books?id=4kZmAwAAQBAJ |year=2014 |publisher=Oxford University Press |isbn=978-0-19-997673-7}}</ref> (following [[drug resistance]]) or [[measles]].<ref name=Fraser-bell2019>{{cite journal |last1=Fraser-bell |first1=C |title=Global Re-emergence of Measles - 2019 update |journal=Global Biosecurity |date=2019 |volume=1 |issue=3 |doi=10.31646/gbio.43 |url=https://www.jglobalbiosecurity.com/articles/10.31646/gbio.43/ |language=en |issn=2652-0036}}</ref> Nosocomial (hospital-acquired) infections, such as [[methicillin-resistant Staphylococcus aureus]] are emerging in hospitals, and are extremely problematic in that they are resistant to many antibiotics.<ref>{{cite journal |last1=Witte |first1=W |title=Increasing incidence and widespread dissemination of methicillin‐resistant Staphylococcus aureus (MRSA) in hospitals in central Europe, with special reference to German hospitals.|journal=Clinical Microbiology and Infection|date=1997|volume=3|issue=4|pages=414–22|doi=10.1111/j.1469-0691.1997.tb00277.x}}</ref> Of growing concern are adverse synergistic interactions between emerging diseases and other infectious and [[non-communicable diseases|non-infectious conditions]] leading to the development of novel [[syndemic]]s. |
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Many EID are [[zoonotic]],<ref name=Woolhouse2005>{{cite journal |last1=Woolhouse |first1=ME |last2=Gowtage-Sequeria |first2=S| title=Host Range and Emerging and Reemerging Pathogens |journal=Emerging Infectious Diseases |date=2005 |volume=11 |page=1842-7 |pmid=16485468 |pmc=3367654 |doi=10.3201/eid1112.050997}}</ref> deriving from pathogens present in animals, with only occasional [[cross-species transmission]] into human populations. For instance, most [[emergent virus]]es are zoonotic<ref name=Woolhouse2005/> (whereas other [[novel virus]]es may have been circulating in the species without being recognized, as occurred with [[hepatitis C]]<ref name=Houghton2009>{{cite journal |author=Houghton M |title=The long and winding road leading to the identification of the hepatitis C virus |journal=Journal of Hepatology |volume=51 |issue=5 |pages=939–48 |date=November 2009 |pmid=19781804 |doi=10.1016/j.jhep.2009.08.004 |url=http://www.journal-of-hepatology.eu/article/S0168-8278%2809%2900535-2/fulltext}}</ref>). |
Many EID are [[zoonotic]],<ref name=Woolhouse2005>{{cite journal |last1=Woolhouse |first1=ME |last2=Gowtage-Sequeria |first2=S| title=Host Range and Emerging and Reemerging Pathogens |journal=Emerging Infectious Diseases |date=2005 |volume=11 |page=1842-7 |pmid=16485468 |pmc=3367654 |doi=10.3201/eid1112.050997}}</ref> deriving from pathogens present in animals, with only occasional [[cross-species transmission]] into human populations. For instance, most [[emergent virus]]es are zoonotic<ref name=Woolhouse2005/> (whereas other [[novel virus]]es may have been circulating in the species without being recognized, as occurred with [[hepatitis C]]<ref name=Houghton2009>{{cite journal |author=Houghton M |title=The long and winding road leading to the identification of the hepatitis C virus |journal=Journal of Hepatology |volume=51 |issue=5 |pages=939–48 |date=November 2009 |pmid=19781804 |doi=10.1016/j.jhep.2009.08.004 |url=http://www.journal-of-hepatology.eu/article/S0168-8278%2809%2900535-2/fulltext}}</ref>). |
Revision as of 18:20, 25 April 2020
An emerging infectious disease (EID) is an infectious disease whose incidence has increased recently (in the past 20 years), and could increase in the near future.[1] Such diseases do not respect national boundaries.[1] The minority that are capable of developing efficient transmission between humans can become major public and global concerns as potential causes of epidemics or pandemics.[2] Their many impacts can be economic and societal, as well as clinical.[3]
Emerging infections account for at least 12% of all human pathogens.[4] EIDs can be caused by newly identified microbes, including novel species or strains of virus[5] (e.g. novel coronaviruses, ebolaviruses, HIV). Some EIDs evolve from a known pathogen, as occurs with new strains of influenza. EIDs may also result from spread of an existing disease to a new population in a different geographic region, as occurs with West Nile fever outbreaks. Some known diseases can also emerge in areas undergoing ecologic transformation (as in the case of Lyme disease[6]). Others can experience a resurgence as a re-emerging infectious disease, like tuberculosis[7] (following drug resistance) or measles.[8] Nosocomial (hospital-acquired) infections, such as methicillin-resistant Staphylococcus aureus are emerging in hospitals, and are extremely problematic in that they are resistant to many antibiotics.[9] Of growing concern are adverse synergistic interactions between emerging diseases and other infectious and non-infectious conditions leading to the development of novel syndemics.
Many EID are zoonotic,[2] deriving from pathogens present in animals, with only occasional cross-species transmission into human populations. For instance, most emergent viruses are zoonotic[2] (whereas other novel viruses may have been circulating in the species without being recognized, as occurred with hepatitis C[10]).
Contributing factors
- Microbial adaption[3] (e.g. genetic drift and genetic shift in Influenza A).
- Changing human susceptibility[3] (e.g. mass immunocompromisation with HIV/AIDS).
- Climate change and weather.[3] For example, diseases transmitted by animal vectors such as mosquitoes (e.g. West Nile fever) are moving further from the tropics as the climate warms).
- Changes in human demographics and travel,[3] facilitating rapid global spread (e.g. SARS-related coronaviruses).
- Economic development; e.g. use of antibiotics to increase meat yield of farmed cows leads to antibiotic resistance
- War and famine.[3]
- Inadequate public health sevices.[3]
- Poverty and social inequality[3] (e.g. tuberculosis is primarily a problem in low-income areas).
- Bioterrorism[3] (e.g. 2001 Anthrax attacks).
- Dam construction and irrigation systems can encourage malaria and other mosquito-borne diseases.
- Anti-vaccination and several other pseudoscience movements (e.g. re-emergence of measles).[11]
- Use of indiscriminate pesticides in industrial farming reduces/eliminates biological controls (e.g. dragonflies, amphibians, insectivorous birds, spiders) of known disease vectors (e.g. mosquito, tick, biting midge).
- The wildlife trade has been linked to zoonotic emergence and spread of new infectious diseases in humans.[12][13] Crowded and unhygienic wet markets (and farms) have been implicated in animal-human tranmission of emergent viruses, including novel coronaviruses and influenza viruses.[14] Complex issues surrounding the commerce and consumption of bushmeat are also of particular concern.[15][16][17]
List
As of 2004, the U.S. National Institute of Allergy and Infectious Diseases recognized the following emerging and re-emerging diseases.[18]
- Acanthamebiasis
- Australian bat lyssavirus
- Babesia, atypical
- Bartonella henselae
- Coronaviruses, including SARS coronavirus
- Ehrlichiosis
- Encephalitozoon cuniculi
- Encephalitozoon hellem
- Enterocytozoon bieneusi
- Helicobacter pylori
- Hendra virus (equine morbilli virus)
- Hepatitis C
- Hepatitis E
- Human herpesvirus 8
- Human herpesvirus 6
- Lyme borreliosis
- Microsporidia
- Parvovirus B19
Re-emerging:
Diseases with bioterrorism potential, CDC category A (most dangerous):
- Anthrax
- Clostridium botulinum
- Tularemia
- Smallpox and other pox viruses
- Viral hemorrhagic fevers
- Yersinia pestis
Diseases with bioterrorism potential, CDC category B:
- Brucella species (brucellosis)
- Burkholderia pseudomallei (melioidosis)
- Burkholderia mallei (glanders)
- Coxiella burnetii (Q fever)
- Epsilon toxin of Clostridium perfringens
- Food-borne and Water-borne Pathogens
- Bacteria
- Campylobacter jejuni
- Diarrheagenic E. coli
- Listeria monocytogenes
- Pathogenic vibrios
- Salmonella
- Shigella species
- Yersinia enterocolitica
- Protozoa
- Fungi
- Viruses:
- Bacteria
- Mosquito-borne encephalitis viruses
- Ricin toxin (from Ricinus communis)
- Staphylococcal enterotoxin B
- Typhus fever (Rickettsia prowazekii)
Diseases with bioterrorism potential, CDC category C (least dangerous):
- Influenza
- Multidrug-resistant tuberculosis (MDR-TB)
- Nipah virus
- Rabies
- SARS coronavirus
- Tick-borne encephalitis virus
- Tick-borne hemorrhagic fever viruses
- Crimean-Congo hemorrhagic fever virus
- Yellow fever
- Other hantaviruses
- Other rickettsias
Since 2004, NIAID has added to its biodefense emerging pathogen list:[19]
- Yersinia pestis (plague, category A)
- Chapare virus (category A areanavirus)
- Lujo (category A arenavirus)
- Chlamydia psittaci (category B)
- Naegleria fowleri (category B)
- Balamuthia mandrillaris (category B)
- St. Louis encephalitis virus (SLEV, category B)
- Tick-borne hemorrhagic fever viruses (category C)
- Bunyaviruses: Severe Fever with Thrombocytopenia Syndrome virus (SFTSV), Heartland virus
- Flaviviruses: Omsk Hemorrhagic Fever virus, Alkhurma virus, Kyasanur Forest virus (reclassified from B to C)
- Powassan virus (Deer Tick virus, category C)
- Chikungunya virus (category C)
- Coccidioides species (category C)
- Human coronavirus HKU1 (category C)
- Middle East respiratory syndrome coronavirus (category C)
- Anaplasmosis
- Aspergillus
- BK virus
- Bordetella pertussis
- Borrelia miyamotoi
- Clostridium difficile
- Cryptococcus gattii
- Enterococcus faecium
- Enterococcus faecalis
- Enterovirus 68
- JC virus
- Leptospirosis
- Measles
- Mucormycosis
- Mumps virus
- Poliovirus
- Zika virus
Methicillin-resistant Staphylococcus aureus
Methicillin-resistant Staphylococcus aureus (MRSA) evolved from Methicillin-susceptible Staphylococcus aureus (MSSA) otherwise known as common S. aureus. Many people are natural carriers of S. aureus, without being affected in any way. MSSA was treatable with the antibiotic methicillin until it acquired the gene for antibiotic resistance.[20] Through genetic mapping of various strains of MRSA, scientists have found that MSSA acquired the mecA gene in the 1960s, which accounts for its pathogenicity, before this it had a predominantly commensal relationship with humans. It is theorized that when this S. aureus strain that had acquired the mecA gene was introduced into hospitals, it came into contact with other hospital bacteria that had already been exposed to high levels of antibiotics. When exposed to such high levels of antibiotics, the hospital bacteria suddenly found themselves in an environment that had a high level of selection for antibiotic resistance, and thus resistance to multiple antibiotics formed within these hospital populations. When S. aureus came into contact with these populations, the multiple genes that code for antibiotic resistance to different drugs were then acquired by MRSA, making it nearly impossible to control.[21] It is thought that MSSA acquired the resistance gene through the horizontal gene transfer, a method in which genetic information can be passed within a generation, and spread rapidly through its own population as was illustrated in multiple studies.[22] Horizontal gene transfer speeds the process of genetic transfer since there is no need to wait an entire generation time for gene to be passed on.[22] Since most antibiotics do not work on MRSA, physicians have to turn to alternative methods based in Darwinian medicine. However, prevention is the most preferred method of avoiding antibiotic resistance. By reducing unnecessary antibiotic use in human and animal populations, antibiotics resistance can be slowed.
See also
References
- ^ a b "Emerging Infectious Diseases - NIOSH Workplace Safety and Health Topic". www.cdc.gov. Centers for Disease Control and Prevention. 17 October 2018. Archived from the original on 18 April 2020.
- ^ a b c Woolhouse, ME; Gowtage-Sequeria, S (2005). "Host Range and Emerging and Reemerging Pathogens". Emerging Infectious Diseases. 11: 1842-7. doi:10.3201/eid1112.050997. PMC 3367654. PMID 16485468.
- ^ a b c d e f g h i Morens DM, Fauci AS (2013). "Emerging infectious diseases: threats to human health and global stability". PLoS Pathogens. 9 (7): e1003467. doi:10.1371/journal.ppat.1003467. PMC 3701702. PMID 23853589.
{{cite journal}}
: CS1 maint: unflagged free DOI (link) - ^ Taylor L.; et al. (2001). "Risk factors for human disease emergence". Philosophical Transactions of the Royal Society B. 356 (1411): 983–9. doi:10.1098/rstb.2001.0888. PMC 1088493. PMID 11516376.
- ^ Fauci AS (2005). "Emerging and reemerging infectious diseases: the perpetual challenge". Academic Medicine. 80 (12): 1079–85. doi:10.1097/00001888-200512000-00002. PMID 16306276.
- ^ Kilpatrick AM, Dobson AD, Levi T, et al. (2017). "Lyme disease ecology in a changing world: consensus, uncertainty and critical gaps for improving control". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 372 (1722). doi:10.1098/rstb.2016.0117. PMC 5413869. PMID 28438910.
- ^ A Dictionary of Epidemiology. Oxford University Press. 2014. p. 92. ISBN 978-0-19-997673-7.
{{cite book}}
: Unknown parameter|editors=
ignored (|editor=
suggested) (help) - ^ Fraser-bell, C (2019). "Global Re-emergence of Measles - 2019 update". Global Biosecurity. 1 (3). doi:10.31646/gbio.43. ISSN 2652-0036.
- ^ Witte, W (1997). "Increasing incidence and widespread dissemination of methicillin‐resistant Staphylococcus aureus (MRSA) in hospitals in central Europe, with special reference to German hospitals". Clinical Microbiology and Infection. 3 (4): 414–22. doi:10.1111/j.1469-0691.1997.tb00277.x.
- ^ Houghton M (November 2009). "The long and winding road leading to the identification of the hepatitis C virus". Journal of Hepatology. 51 (5): 939–48. doi:10.1016/j.jhep.2009.08.004. PMID 19781804.
- ^ Patricia, Calderón Rodríguez Nelly; Zulay, Jerez Pacheco Yary; Carlos, Ruvalcaba Ledezma Jesús; et al. (2019). "The Influence of Antivaccination Movements on the Re-emergence of Measles". Journal of Pure and Applied Microbiology. 13 (1): 127–132. doi:10.22207/JPAM.13.1.13.
- ^ Smith KM, Anthony SJ, Switzer WM, et al. (2012). "Zoonotic viruses associated with illegally imported wildlife products". Plos One. 7 (1): e29505. doi:10.1371/journal.pone.0029505. PMC 3254615. PMID 22253731.
{{cite journal}}
: CS1 maint: unflagged free DOI (link) - ^ Smith, KF; Schloegel, LM; Rosen, GE (2012). "Wildlife Trade and the Spread of Disease". New Directions in Conservation Medicine: Applied Cases of Ecological Health. Oxford University Press. pp. 151–163. ISBN 978-0-19-990905-6.
{{cite book}}
: Unknown parameter|editors=
ignored (|editor=
suggested) (help) - ^ Chan JF, To KK, Tse H, et al. (2013). "Interspecies transmission and emergence of novel viruses: lessons from bats and birds". Trends in Microbiology. 21 (10): 544–55. doi:10.1016/j.tim.2013.05.005. PMC 7126491. PMID 23770275.
- ^ LeBreton, M; Pike, BL; Saylors, KE; et al. (2012). "Bushmeat and Infectious Disease Emergence". New Directions in Conservation Medicine: Applied Cases of Ecological Health. Oxford University Press. pp. 164–178. ISBN 978-0-19-990905-6.
{{cite book}}
: Unknown parameter|editors=
ignored (|editor=
suggested) (help) - ^ Murray KA, Allen T, Loh E, et al. (2015). "Emerging Viral Zoonoses from Wildlife Associated with Animal-Based Food Systems: Risks and Opportunities". In Russell MJ, Doyle MP (eds.). Food Safety Risks from Wildlife. Springer. pp. 31–57. doi:10.1007/978-3-319-24442-6_2. ISBN 978-3-319-24442-6.
- ^ Kurpiers LA, Schulte-Herbrüggen B, Ejotre I, et al. (2016). "Bushmeat and Emerging Infectious Diseases: Lessons from Africa". In Angelici F (ed.). Problematic Wildlife: A Cross-Disciplinary Approach. Springer. pp. 31–57. doi:10.1007/978-3-319-22246-2_24. ISBN 978-3-319-22246-2.
- ^ http://www.niaid.nih.gov/about/whoWeAre/profile/fy2004/Documents/research_emerging_re-emerging.pdf
- ^ "NIAID Emerging Infectious Diseases/ Pathogens". www.niaid.nih.gov. NIH - National Institute of Allergy and Infectious Diseases. 26 July 2018. Archived from the original on 18 April 2020.
- ^ Witte, W., Kresken, M., Braulke, C., & Cuny, C. (1997). Increasing incidence and widespread dissemination of methicillin‐resistant Staphylococcus aureus (MRSA) in hospitals in central Europe, with special reference to German hospitals. Clinical Microbiology and Infection, 3(4), 414-422.
- ^ Benson, M. A., Ohneck, E. A., Ryan, C., Alonzo, F., Smith, H., Narechania, A., & Torres, V. J. (2014). Evolution of hypervirulence by a MRSA clone through acquisition of a transposable element. Molecular microbiology, 93(4), 664-681.
- ^ a b Krishnapillai, V. (1996). Horizontal gene transfer. Journal of Genetics, 75(2), 219-232.
Further reading
- Nathan Wolfe (2012). The Viral Storm: The Dawn of a New Pandemic Age. St. Martin's Griffin. ISBN 978-1250012210.
External links
- Website of Emerging Infectious Diseases, an open-access, peer-review journal published by the Centers for Disease Control and Prevention (CDC)