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[[Category:Campylobacterota]]
[[Category:Bacteria described in 1993]]
{{Short description|Species of bacterium}}
{{Short description|Species of bacterium}}
[[Category:Campylobacterota]]
{{Speciesbox
[[Category:Bacteria described in 1993]]
| genus = Campylobacter
{{Taxobox
| species = showae
| name = ''Campylobacter Showae''
| authority = Etoh et al. 1993
| domain = [[Bacteria]]
| phylum = [[Proteobacteria]]
| classis = [[Epsilonproteobacteria]]
| ordo = [[Campylobacterales]]
| familia = [[Campylobacteraceae]]
| genus = [[Campylobacter]]
| species = [[C. showae]]
| binomial = ''Campylobacter Showae''
| binomial_authority = Etoh et al. 1993
| type_species = SUA4 (ATCC 51146)
}}
}}


'''''Campylobacter showae''''' is a [[Gram-negative bacteria|Gram-negative]], [[chemoheterotrophic]], [[Microaerophile|microaerophilic]], motile bacteria belonging to the ''Campylobacter'' Genus. <ref name=":0">{{Cite journal |last=Etoh |first=Yumiko |last2=Dewhirst |first2=Floyd E. |last3=Paster |first3=Bruce J. |last4=Yamamoto |first4=Ayako |last5=Goto |first5=Nobuichi |date=1993 |title=Campylobacter showae sp. nov., Isolated from the Human Oral Cavity |url=https://www.microbiologyresearch.org/content/journal/ijsem/10.1099/00207713-43-4-631 |journal=International Journal of Systematic and Evolutionary Microbiology |volume=43 |issue=4 |pages=631–639 |doi=10.1099/00207713-43-4-631 |issn=1466-5034}}</ref><ref name=":3">{{Citation |last=Silva |first=Willian C. |title=Campylobacter : An Important Food Safety Issue |date=2018 |work=Food Safety and Preservation |pages=391–430 |url=https://linkinghub.elsevier.com/retrieve/pii/B9780128149560000135 |access-date=2024-04-16 |publisher=Elsevier |language=en |doi=10.1016/b978-0-12-814956-0.00013-5 |isbn=978-0-12-814956-0 |last2=Targino |first2=Brenda N. |last3=Gonçalves |first3=Amanda G. |last4=Silva |first4=Marcio R. |last5=Hungaro |first5=Humberto M.}}</ref> This bacterial species was first isolated from plaque samples taken from the gingival crevices of the human oral cavity but has since also been found in colonic tissues and stool. <ref name=":0" /> Since its discovery, ''C. showae'' has been implicated in various medical conditions, including [[Crohn's disease]], [[periodontitis]], [[inflammatory bowel disease]], and [[ulcerative colitis]] due to its pathogenic nature.<ref name=":3" /><ref name=":4">{{Cite journal |last=Macuch |first=P.J. |last2=Tanner |first2=A.C.R. |date=2000-02 |title=Campylobacter Species in Health, Gingivitis, and Periodontitis |url=http://journals.sagepub.com/doi/10.1177/00220345000790021301 |journal=Journal of Dental Research |language=en |volume=79 |issue=2 |pages=785–792 |doi=10.1177/00220345000790021301 |issn=0022-0345}}</ref><ref name=":2">{{Cite journal |last=Hsu |first=Tiffany |last2=Gemmell |first2=Matthew R. |last3=Franzosa |first3=Eric A. |last4=Berry |first4=Susan |last5=Mukhopadhya |first5=Indrani |last6=Hansen |first6=Richard |last7=Michaud |first7=Monia |last8=Nielsen |first8=Hans |last9=Miller |first9=William G. |last10=Nielsen |first10=Henrik |last11=Bajaj-Elliott |first11=Mona |last12=Huttenhower |first12=Curtis |last13=Garrett |first13=Wendy S. |last14=Hold |first14=Georgina L. |date=2019 |title=Comparative genomics and genome biology of Campylobacter showae |url=https://www.tandfonline.com/doi/full/10.1080/22221751.2019.1622455 |journal=Emerging Microbes & Infections |language=en |volume=8 |issue=1 |pages=827–840 |doi=10.1080/22221751.2019.1622455 |issn=2222-1751 |pmc=PMC6567213 |pmid=31169073}}</ref>
'''''Campylobacter showae''''' is a species of ''[[Campylobacter]]'' found in humans. It is [[gram-negative]], straight rod-shaped, [[motile]] by means of multiple unipolar [[flagellum|flagella]]. It is [[asaccharolytic]] and prefers an anaerobic atmosphere. SU A4 (= ATCC 51146) is its type strain.<ref name="EtohDewhirst1993">{{cite journal|last1=Etoh|first1=Y.|last2=Dewhirst|first2=F. E.|last3=Paster|first3=B. J.|last4=Yamamoto|first4=A.|last5=Goto|first5=N.|title=Campylobacter showae sp. nov., Isolated from the Human Oral Cavity|journal=International Journal of Systematic Bacteriology|volume=43|issue=4|year=1993|pages=631–639|issn=0020-7713|doi=10.1099/00207713-43-4-631|pmid=7694633|doi-access=free}}</ref> Its genome has been sequenced.<ref name="TayKaakoush2013">{{cite journal|last1=Tay|first1=A. P.|last2=Kaakoush|first2=N. O.|last3=Deshpande|first3=N. P.|last4=Chen|first4=Z.|last5=Mitchell|first5=H.|last6=Wilkins|first6=M. R.|title=Genome Sequence of Campylobacter showae UNSWCD, Isolated from a Patient with Crohn's Disease|journal=Genome Announcements|volume=1|issue=1|year=2013|pages=e00193–12–e00193–12|issn=2169-8287|doi=10.1128/genomeA.00193-12|pmid=23409253|pmc=3569271}}</ref>


==References==
== Taxonomy ==
{{Reflist}}


=== '''Taxonomic Description''' ===
==Further reading==
''Campylobacter showae'' is a member of the Bacteria domain, the Proteobacteria phylum, the Epsilonproteobacteria class, the Campylobacterales order, the Campylobacteraceae family, the ''Campylobacter'' genus, and the ''showae'' species.<ref name=":3" /> The ''Campylobacter'' genus is in a state of constant evolution as a result of the discovery of new species and the reclassification of others but currently consists of 27 species.<ref name=":3" />
*{{cite book |author1=Michael E. Konkel |author2=Ketley, Julian M. |title=Campylobacter: Molecular And Cellular Biology |edition= |language= |publisher=Horizon Bioscience |location= |year=2005 |pages= |quote= |isbn=1-904933-05-X |oclc= |doi= |url= }}
*{{cite journal|last1=Macuch|first1=P.J.|last2=Tanner|first2=A.C.R.|title=Campylobacter Species in Health, Gingivitis, and Periodontitis|journal=Journal of Dental Research|volume=79|issue=2|year=2000|pages=785–792|issn=0022-0345|doi=10.1177/00220345000790021301|pmid=10728981|s2cid=21871310}}
*{{cite journal|last1=Man|first1=Si Ming|last2=Kaakoush|first2=Nadeem O.|last3=Leach|first3=Steven T.|last4=Nahidi|first4=Lily|last5=Lu|first5=Hao K.|last6=Norman|first6=Jennifer|last7=Day|first7=Andrew S.|last8=Zhang|first8=Li|last9=Mitchell|first9=Hazel M.|title=Host Attachment, Invasion, and Stimulation of Proinflammatory Cytokines byCampylobacter concisusand Other Non–Campylobacter jejuni CampylobacterSpecies|journal=The Journal of Infectious Diseases|volume=202|issue=12|year=2010|pages=1855–1865|issn=0022-1899|doi=10.1086/657316|pmid=21050118|doi-access=free}}
*{{cite journal|last1=Suzuki|first1=Jun|last2=Ito|first2=Kenta|last3=Hadano|first3=Yoshiro|last4=Kawamura|first4=Ichiro|last5=Kurai|first5=Hanako|last6=Sugiyama|first6=Tomoyo|last7=Okinaka|first7=Keiji|last8=Ohkusu|first8=Kiyofumi|last9=Ohmagari|first9=Norio|title=Campylobacter showae bacteremia with cholangitis|journal=Journal of Infection and Chemotherapy|volume=19|issue=5|year=2013|pages=960–963|issn=1341-321X|doi=10.1007/s10156-012-0524-2|pmid=23183773|s2cid=44716537}}


=== Neighboring Taxa ===
==External links==
A [[pan-genome]] analysis, looking at a set of single-copy conserved core genes between 39 ''Campylobacter'' species, found that ''C. showae'' was most closely related to ''[[Campylobacter rectus]]'', with ''C. showae'' and ''C. rectus'' constituting more ancient lineages within the ''Campylobacter'' genus.<ref name=":1">{{Cite journal |last=Zhong |first=Chaofang |last2=Qu |first2=Bingpeng |last3=Hu |first3=Gang |last4=Ning |first4=Kang |date=2022-10-26 |editor-last=Garcia-Solache |editor-first=Monica Adriana |title=Pan-Genome Analysis of Campylobacter: Insights on the Genomic Diversity and Virulence Profile |url=https://journals.asm.org/doi/10.1128/spectrum.01029-22 |journal=Microbiology Spectrum |language=en |volume=10 |issue=5 |doi=10.1128/spectrum.01029-22 |issn=2165-0497 |pmc=PMC9602946 |pmid=36069574}}</ref> A separate analysis of 16S rRNA sequences, comparing 1400 base positions in 21 ''Campylobacter'', ''[[Wolinella]]'', and ''[[Helicobacter]]'' bacterial strains, found that ''C. showae'' was most closely related to [[Campylobacter rectus|''Campylobacter rectus'']], ''[[Campylobacter curvus]]'', and [[Campylobacter concisus|''Campylobacter concisus'']], with their sequences differing by 1.3%, 2.8%, and 4.9% respectively.<ref name=":0" /> These four ''Campylobacter'' species share many similarities including their known source, being dogs and humans, and in the diseases they cause in humans, with all four being implicated in gastrointestinal diseases such as [[gastroenteritis]] or [[ulcerative colitis]] and oral diseases like [[periodontitis]].<ref name=":3" />
*{{EOL}}
*[https://lpsn.dsmz.de/genus/campylobacter LPSN]
*[http://bacdive.dsmz.de/index.php?search=2136&submit=Search Type strain of ''Campylobacter showae'' at Bac''Dive'' - the Bacterial Diversity Metadatabase]


== Discovery ==
{{Taxonbar|from=Q16975403}}
''Campylobacter showae'' was first discovered in October of 1993 by researchers Yumiko Etoh, Floyd Dewhirst, Bruce Paster, Ayako Yamamoto, and Nobuichi Goto from the Showa University School of Dentistry and the Forsyth Dental Center.<ref name=":0" /> The bacteria was obtained via isolation from human gingival crevices and was subsequently differentiated fro based on its morphological differences such as their number of flagella.<ref name=":0" /> While the organism did show several biochemical similarities to ''[[Campylobacter Curvus|Campylobacter curvus]]'' and ''[[Campylobacter rectus]]'', these newly identified microbes had 2-5 flagella compared to the standard 1 in the 2 previously named organisms. <ref name=":0" />


=== Isolation and Characterization ===
[[Category:Campylobacterota]]
''C. showae'' was first isolated from plaque within the gingival crevices of 9 healthy adults using plates containing CBRCA, a medium containing reinforced clostridial agar, 5% horse blood, 0.03% China Blue, 0.2% [[sodium formate]], 0.3% [[sodium fumarate]] and [[menadione]].<ref name=":0" /> Being selective for ''[[Campylobacter]], [[Selenomonad|Selenomonas]], [[Fusobacterium]],'' ''[[Veillonella]],'' and ''[[Bacteroides]]'' strains, the resulting growth on the CBRCA plates allowed for the minimization of interference from other microorganisms and increased diagnostic sensitivity.<ref name=":0" /> The cultures were subsequently cultivated on brain heart infusion agar plates and incubated under [[anaerobic]] conditions, in a 80% nitrogen, 10% carbon dioxide, 10% hydrogen atmosphere.<ref name=":0" /> Additionally, their ability to grow under [[Microaerophile|microaerophilic]] conditions was tested via a [[Gas-pak|Gas-Pak]] jar using blood agar plates with added sodium formate and fumarate at 0.2% and 0.3% concentrations respectively.<ref name=":0" />
[[Category:Bacteria described in 1993]]


Characterization of the isolated strains was performed by electron microscopy, allowing for observation of cell structure and morphology. Additionally, several tests were performed to deduce the metabolic activities of the organisms including 1) testing for the presence of catalase enzyme, characteristic of facultative anaerobes and aerobes; 2) testing for [[Oxidase test|oxidase]] activity to detect the presence of [[cytochrome c oxidase]], an enzyme involved in aerobic respiration; 3) detection of enzymes that allow for Indoxyl acetate hydrolysis, allowing for the differentiation of ''Campylobacter'' subspecies; 4) detection of the [[alkaline phosphatase]] and [[Gamma-glutamyltransferase|gamma-glutamyl transpeptidase]] enzymes, providing metabolic information for species differentiation; 5) detection of the [[arylsulfatase]] to indicate the organism's ability to hydrolyze sulfate ester bonds; 6) detection of the [[urease]] enzyme which is involved in urea hydrolysis; 7) the ability for the organism to reduce nitrate and nitrite in order to reduce hydrogen sulfide; 8) detection of [[lysine]] and [[ornithine decarboxylase]], an enzyme that allows for the decarboxylation of lysine and ornithine amino acids; 9) resistance to antibiotics such as [[nalidixic acid]], to differentiate species based on antibiotic resistance, and more.<ref name=":0" /> To further differentiate species with similar phenotypes, Further, [[SDS-PAGE|SDS-page]], to compare the protein profiles of each bacteria; DNA-DNA homology, to determine relatedness or genetic similarity between species; and 16S rRNA sequence comparisons, to deduce ''C. showae''<nowiki/>'s phylogenetic relationships, were also performed. As a result of these tests and experiments, ''C. showae'' was successfully isolated, characterized, and differentiated from its neighboring taxa.<ref name=":0" />


=== Classification as a Novel Species ===
{{Campylobacterota-stub}}
''C. showae'' was given the distinction as a new species based on phylogenetic analysis performed by 16S rRNA sequence comparisons.<ref name=":0" /> Two previously described, but unnamed, ''C. showae'' strains were isolated and it was found that they displayed the closest relation to ''C. rectus'', with their rRNA sequences differing at 1.35% of the positions – the same percent that ''[[Campylobacter coli]]'' and [[Campylobacter jejuni|''Campylobacter jejuni'']] or ''[[Campylobacter lari]]'' and ''C. jejuni'' differed.<ref name=":0" /> As a result of this analysis, the researchers concluded that these species should be placed in the ''Campylobacter'' genus and exhibit adequate genetic distance to justify classification as a novel species.<ref name=":0" />

== Morphology ==
''C. showae'' exhbits a curved-rod or spiral shape with round ends, measuring 2-5μm long and 0.5-0.8μm wide.<ref name=":0" /> Although species of ''Campylobacter'', such as ''C. curvus'' and ''C. rectus'', primarily present only one polar flagellum, ''C. showae'' express 2-5 unipolar flagella, each with a diameter of 15-20nm.<ref name=":0" /> Additionally, ''C. showae'' is Gram-negative and thus exhibit a cell wall comprised of a cytoplasmic membrane and outer membrane in which a thin [[peptidoglycan layer]] resides in the [[Periplasm|periplasmic]] space.<ref name=":0" /> ''C. showae'' cells were not observed to have any surface layer, unlike ''C. rectus'' cells which assemble an S-layer or a crystalline layer of macromolecular subunits on their cell surface for protection.<ref name=":0" />

== Metabolism ==
''C. showae'', along with other bacteria in the ''Campylobacter'' genus, are primarily [[chemoheterotrophic]] organisms, deriving energy mainly from citric acid cycle intermediates and amino acids via oxidation.<ref name=":3" /> Lacking the important glycolytic pathway enzyme, 6-phosphofructokinase, ''Campylobacter'' species are asaccharolytic, being unable to oxidize or ferment carbohydrates for use in its metabolism.<ref name=":3" /> These organisms can also perform respiration to conserve energy, coupling the oxidation of formate and hydrogen to the reduction of nitrate, sulfites, fumarates, oxygen and other electron acceptors to generate ATP via electron transport phosphorylation.<ref name=":3" /> Being a microaerophilic organism, ''C. showae'' can only tolerate an atmospheric oxygen concentration below normal atmospheric pressure, observed to grow best under atmospheric conditions of only 3%-6% Oxygen.<ref name=":3" />

== Pathogenicity ==
The multiple flagella of ''C. showae'' are often found to be 2 to 3 times their attached cells in length and move in a corkscrew motion, allowing for the cell to be motile.<ref name=":3" /> This characteristic enables ''C. showae'' and other pathogenic species of the ''Campylobacter'' genus to perform [[chemotaxis]] in response to mediating chemoattractants.<ref name=":3" /> For instance, ''Campylobacter'' species can migrate towards metabolic substrates or electron donors and acceptors, allowing them to specifically locate and target sites for cellular invasion.<ref name=":3" /> After overcoming the host's protective mucus layer, ''Campylobacter'' species use a multitude of adhesion-mediating factors such as CadF, an outer-membrane adhesin protein that binds to [[fibronectin]], to facilitate adherence to host cells and induce internalization.<ref name=":3" /> By residing within a vacuole or other membrane-bound compartment of the host cell, ''Campylobacter'' can thus avoid the defense mechanisms of the host cell and survive by utilizing its nutrients until conditions permit a cytotoxic response to be induced.<ref name=":3" />

== Genomics ==
A 2019 study conducted by Tiffany Hsu and others describes the genome biology and comparative genomics of ''C. showae''.<ref name=":2" /> Short read [[Illumina sequencing]] was conducted for 8 strains of this bacteria with 4 being subject to PacBio RSII [[Long-read sequencing|long read sequencing]].<ref name=":2" /> The sizes of each genome ranged from 2.1Mb-2.6Mb with an estimated >98% completeness by [[Busco|BUSCO]] with the exception of 2 strains at 92.9% and 97.6%.<ref name=":2" /> After being analyzed via the presence and absence of gene families and differences were found between the strains.<ref name=":2" /> For example, the T4SS gene, which allows for the transfer of protein substrates and DNA to host cells, was found only in the invasive or adherent strains of ''C. showae''.<ref name=":2" /> Additionally, genes for methyl-accepting chemotaxis proteins were only found in ''C. showae'' strains that reside in the subgingival plaque of the oral cavity.<ref name=":2" />

== Ecology ==
''C. showae'' was initially isolated from human gingival crevices, residing in the human oral mucosa and within dental plaque biofilms, and has also been observed in human colonic tissues and stool.<ref name=":0" /><ref name=":2" /> Exhibiting a respiratory-type metabolism, ''Campylobacter'' species require oxygen for energy production and growth.<ref name=":3" /> However, they are [[Microaerophile|microaerophilic]], meaning they can only tolerate an atmospheric oxygen concentration below normal atmospheric pressure and have been observed to grow best under atmospheric conditions of only 3%-6% Oxygen.<ref name=":3" /> ''C. showae'', along with other human and animal pathogenic species in this genus, are mesophilic and grow best in conditions ranging from 25ºC to 45.4ºC.<ref name=":3" /> Organisms of this genus display neutrophilic characteristics, growing best in a pH range of 6.5-7.5 and are unable to survive below a pH 4.9 or above a pH of 9.0.<ref name=":3" /> Unlike other food-borne pathogens, members of the ''Campylobacter'' genus do not display the same extent of adaptive stress responses, being vulnerable to [[aeration]], [[desiccation]], [[osmotic stress]], low water activity, and high salt concentrations.<ref name=":3" /> These characteristics are indicative of the species' adaptations to live in a host environment such as within the human oral cavity or gastrointestinal tract, in which temperature and nutrient availability remain constant.<ref name=":3" />

== Importance ==
''C. showae'' has been implicated in numerous human health conditions. For example, ''C. showae'' has historically been linked to gum disease, also known as periodontal disease.<ref name=":4" /> Periodontal disease can be characterized by the infection of the gingiva, or gum tissue, resulting in symptoms like inflammation, bleeding on probing, and periodontal attachment loss.<ref name=":4" /> ''C. showae'' can contribute to the development of gum disease by adhering to oral epithelial cells and releasing [[Proinflammatory cytokines|pro-inflammatory cytokines]] like [[IL-1β]] and [[IL8 (gene)|IL-8]], resulting in tissue damage.<ref name=":4" /><ref name=":2" /> ''C. showae'' has also been linked to several diseases marked by persistant inflammation of a individual's digestive tract, including [[Crohn's disease]] and [[ulcerative colitis]].<ref name=":3" /> Having the ability to invade and colonize the intestinal mucosa, ''C. showae'' can adhere and penetrate the epithelial cells lining intestinal tract once in the gut, resulting in an immune response triggering inflammation.<ref name=":3" /><ref name=":2" /> As a result of contributing and exacerbating gut inflammation, ''C. showae'' can also potentially increase the risk of developing colorectal cancer, which has been linked to chronic gut inflammation.<ref>{{Cite journal |last=Warren |first=René L |last2=Freeman |first2=Douglas J |last3=Pleasance |first3=Stephen |last4=Watson |first4=Peter |last5=Moore |first5=Richard A |last6=Cochrane |first6=Kyla |last7=Allen-Vercoe |first7=Emma |last8=Holt |first8=Robert A |date=2013-12 |title=Co-occurrence of anaerobic bacteria in colorectal carcinomas |url=https://microbiomejournal.biomedcentral.com/articles/10.1186/2049-2618-1-16 |journal=Microbiome |language=en |volume=1 |issue=1 |doi=10.1186/2049-2618-1-16 |issn=2049-2618 |pmc=PMC3971631 |pmid=24450771}}</ref> However, research must be conducted to fully understand ''C. showae’s'' role in these health conditions and if a true causal relationship exists. Further research into ''C. showae's'' biology and pathogenicity can also provide valuable insights into disease prevention strategies, bacterial pathogenesis, and the consequences of bacterial dysbiosis in the human body.

==References==
<references />
<ref name=":0" /><ref name=":1" /><ref name=":2" />
<references />

Revision as of 05:31, 1 May 2024

Campylobacter Showae
Scientific classification
Domain:
Phylum:
Class:
Order:
Family:
Genus:
Species:
Binomial name
Campylobacter Showae
Etoh et al. 1993
Type species
SUA4 (ATCC 51146)

Campylobacter showae is a Gram-negative, chemoheterotrophic, microaerophilic, motile bacteria belonging to the Campylobacter Genus. [1][2] This bacterial species was first isolated from plaque samples taken from the gingival crevices of the human oral cavity but has since also been found in colonic tissues and stool. [1] Since its discovery, C. showae has been implicated in various medical conditions, including Crohn's disease, periodontitis, inflammatory bowel disease, and ulcerative colitis due to its pathogenic nature.[2][3][4]

Taxonomy

Taxonomic Description

Campylobacter showae is a member of the Bacteria domain, the Proteobacteria phylum, the Epsilonproteobacteria class, the Campylobacterales order, the Campylobacteraceae family, the Campylobacter genus, and the showae species.[2] The Campylobacter genus is in a state of constant evolution as a result of the discovery of new species and the reclassification of others but currently consists of 27 species.[2]

Neighboring Taxa

A pan-genome analysis, looking at a set of single-copy conserved core genes between 39 Campylobacter species, found that C. showae was most closely related to Campylobacter rectus, with C. showae and C. rectus constituting more ancient lineages within the Campylobacter genus.[5] A separate analysis of 16S rRNA sequences, comparing 1400 base positions in 21 Campylobacter, Wolinella, and Helicobacter bacterial strains, found that C. showae was most closely related to Campylobacter rectus, Campylobacter curvus, and Campylobacter concisus, with their sequences differing by 1.3%, 2.8%, and 4.9% respectively.[1] These four Campylobacter species share many similarities including their known source, being dogs and humans, and in the diseases they cause in humans, with all four being implicated in gastrointestinal diseases such as gastroenteritis or ulcerative colitis and oral diseases like periodontitis.[2]

Discovery

Campylobacter showae was first discovered in October of 1993 by researchers Yumiko Etoh, Floyd Dewhirst, Bruce Paster, Ayako Yamamoto, and Nobuichi Goto from the Showa University School of Dentistry and the Forsyth Dental Center.[1] The bacteria was obtained via isolation from human gingival crevices and was subsequently differentiated fro based on its morphological differences such as their number of flagella.[1] While the organism did show several biochemical similarities to Campylobacter curvus and Campylobacter rectus, these newly identified microbes had 2-5 flagella compared to the standard 1 in the 2 previously named organisms. [1]

Isolation and Characterization

C. showae was first isolated from plaque within the gingival crevices of 9 healthy adults using plates containing CBRCA, a medium containing reinforced clostridial agar, 5% horse blood, 0.03% China Blue, 0.2% sodium formate, 0.3% sodium fumarate and menadione.[1] Being selective for Campylobacter, Selenomonas, Fusobacterium, Veillonella, and Bacteroides strains, the resulting growth on the CBRCA plates allowed for the minimization of interference from other microorganisms and increased diagnostic sensitivity.[1] The cultures were subsequently cultivated on brain heart infusion agar plates and incubated under anaerobic conditions, in a 80% nitrogen, 10% carbon dioxide, 10% hydrogen atmosphere.[1] Additionally, their ability to grow under microaerophilic conditions was tested via a Gas-Pak jar using blood agar plates with added sodium formate and fumarate at 0.2% and 0.3% concentrations respectively.[1]

Characterization of the isolated strains was performed by electron microscopy, allowing for observation of cell structure and morphology. Additionally, several tests were performed to deduce the metabolic activities of the organisms including 1) testing for the presence of catalase enzyme, characteristic of facultative anaerobes and aerobes; 2) testing for oxidase activity to detect the presence of cytochrome c oxidase, an enzyme involved in aerobic respiration; 3) detection of enzymes that allow for Indoxyl acetate hydrolysis, allowing for the differentiation of Campylobacter subspecies; 4) detection of the alkaline phosphatase and gamma-glutamyl transpeptidase enzymes, providing metabolic information for species differentiation; 5) detection of the arylsulfatase to indicate the organism's ability to hydrolyze sulfate ester bonds; 6) detection of the urease enzyme which is involved in urea hydrolysis; 7) the ability for the organism to reduce nitrate and nitrite in order to reduce hydrogen sulfide; 8) detection of lysine and ornithine decarboxylase, an enzyme that allows for the decarboxylation of lysine and ornithine amino acids; 9) resistance to antibiotics such as nalidixic acid, to differentiate species based on antibiotic resistance, and more.[1] To further differentiate species with similar phenotypes, Further, SDS-page, to compare the protein profiles of each bacteria; DNA-DNA homology, to determine relatedness or genetic similarity between species; and 16S rRNA sequence comparisons, to deduce C. showae's phylogenetic relationships, were also performed. As a result of these tests and experiments, C. showae was successfully isolated, characterized, and differentiated from its neighboring taxa.[1]

Classification as a Novel Species

C. showae was given the distinction as a new species based on phylogenetic analysis performed by 16S rRNA sequence comparisons.[1] Two previously described, but unnamed, C. showae strains were isolated and it was found that they displayed the closest relation to C. rectus, with their rRNA sequences differing at 1.35% of the positions – the same percent that Campylobacter coli and Campylobacter jejuni or Campylobacter lari and C. jejuni differed.[1] As a result of this analysis, the researchers concluded that these species should be placed in the Campylobacter genus and exhibit adequate genetic distance to justify classification as a novel species.[1]

Morphology

C. showae exhbits a curved-rod or spiral shape with round ends, measuring 2-5μm long and 0.5-0.8μm wide.[1] Although species of Campylobacter, such as C. curvus and C. rectus, primarily present only one polar flagellum, C. showae express 2-5 unipolar flagella, each with a diameter of 15-20nm.[1] Additionally, C. showae is Gram-negative and thus exhibit a cell wall comprised of a cytoplasmic membrane and outer membrane in which a thin peptidoglycan layer resides in the periplasmic space.[1] C. showae cells were not observed to have any surface layer, unlike C. rectus cells which assemble an S-layer or a crystalline layer of macromolecular subunits on their cell surface for protection.[1]

Metabolism

C. showae, along with other bacteria in the Campylobacter genus, are primarily chemoheterotrophic organisms, deriving energy mainly from citric acid cycle intermediates and amino acids via oxidation.[2] Lacking the important glycolytic pathway enzyme, 6-phosphofructokinase, Campylobacter species are asaccharolytic, being unable to oxidize or ferment carbohydrates for use in its metabolism.[2] These organisms can also perform respiration to conserve energy, coupling the oxidation of formate and hydrogen to the reduction of nitrate, sulfites, fumarates, oxygen and other electron acceptors to generate ATP via electron transport phosphorylation.[2] Being a microaerophilic organism, C. showae can only tolerate an atmospheric oxygen concentration below normal atmospheric pressure, observed to grow best under atmospheric conditions of only 3%-6% Oxygen.[2]

Pathogenicity

The multiple flagella of C. showae are often found to be 2 to 3 times their attached cells in length and move in a corkscrew motion, allowing for the cell to be motile.[2] This characteristic enables C. showae and other pathogenic species of the Campylobacter genus to perform chemotaxis in response to mediating chemoattractants.[2] For instance, Campylobacter species can migrate towards metabolic substrates or electron donors and acceptors, allowing them to specifically locate and target sites for cellular invasion.[2] After overcoming the host's protective mucus layer, Campylobacter species use a multitude of adhesion-mediating factors such as CadF, an outer-membrane adhesin protein that binds to fibronectin, to facilitate adherence to host cells and induce internalization.[2] By residing within a vacuole or other membrane-bound compartment of the host cell, Campylobacter can thus avoid the defense mechanisms of the host cell and survive by utilizing its nutrients until conditions permit a cytotoxic response to be induced.[2]

Genomics

A 2019 study conducted by Tiffany Hsu and others describes the genome biology and comparative genomics of C. showae.[4] Short read Illumina sequencing was conducted for 8 strains of this bacteria with 4 being subject to PacBio RSII long read sequencing.[4] The sizes of each genome ranged from 2.1Mb-2.6Mb with an estimated >98% completeness by BUSCO with the exception of 2 strains at 92.9% and 97.6%.[4] After being analyzed via the presence and absence of gene families and differences were found between the strains.[4] For example, the T4SS gene, which allows for the transfer of protein substrates and DNA to host cells, was found only in the invasive or adherent strains of C. showae.[4] Additionally, genes for methyl-accepting chemotaxis proteins were only found in C. showae strains that reside in the subgingival plaque of the oral cavity.[4]

Ecology

C. showae was initially isolated from human gingival crevices, residing in the human oral mucosa and within dental plaque biofilms, and has also been observed in human colonic tissues and stool.[1][4] Exhibiting a respiratory-type metabolism, Campylobacter species require oxygen for energy production and growth.[2] However, they are microaerophilic, meaning they can only tolerate an atmospheric oxygen concentration below normal atmospheric pressure and have been observed to grow best under atmospheric conditions of only 3%-6% Oxygen.[2] C. showae, along with other human and animal pathogenic species in this genus, are mesophilic and grow best in conditions ranging from 25ºC to 45.4ºC.[2] Organisms of this genus display neutrophilic characteristics, growing best in a pH range of 6.5-7.5 and are unable to survive below a pH 4.9 or above a pH of 9.0.[2] Unlike other food-borne pathogens, members of the Campylobacter genus do not display the same extent of adaptive stress responses, being vulnerable to aeration, desiccation, osmotic stress, low water activity, and high salt concentrations.[2] These characteristics are indicative of the species' adaptations to live in a host environment such as within the human oral cavity or gastrointestinal tract, in which temperature and nutrient availability remain constant.[2]

Importance

C. showae has been implicated in numerous human health conditions. For example, C. showae has historically been linked to gum disease, also known as periodontal disease.[3] Periodontal disease can be characterized by the infection of the gingiva, or gum tissue, resulting in symptoms like inflammation, bleeding on probing, and periodontal attachment loss.[3] C. showae can contribute to the development of gum disease by adhering to oral epithelial cells and releasing pro-inflammatory cytokines like IL-1β and IL-8, resulting in tissue damage.[3][4] C. showae has also been linked to several diseases marked by persistant inflammation of a individual's digestive tract, including Crohn's disease and ulcerative colitis.[2] Having the ability to invade and colonize the intestinal mucosa, C. showae can adhere and penetrate the epithelial cells lining intestinal tract once in the gut, resulting in an immune response triggering inflammation.[2][4] As a result of contributing and exacerbating gut inflammation, C. showae can also potentially increase the risk of developing colorectal cancer, which has been linked to chronic gut inflammation.[6] However, research must be conducted to fully understand C. showae’s role in these health conditions and if a true causal relationship exists. Further research into C. showae's biology and pathogenicity can also provide valuable insights into disease prevention strategies, bacterial pathogenesis, and the consequences of bacterial dysbiosis in the human body.

References

  1. ^ a b c d e f g h i j k l m n o p q r s t Etoh, Yumiko; Dewhirst, Floyd E.; Paster, Bruce J.; Yamamoto, Ayako; Goto, Nobuichi (1993). "Campylobacter showae sp. nov., Isolated from the Human Oral Cavity". International Journal of Systematic and Evolutionary Microbiology. 43 (4): 631–639. doi:10.1099/00207713-43-4-631. ISSN 1466-5034.
  2. ^ a b c d e f g h i j k l m n o p q r s t u v Silva, Willian C.; Targino, Brenda N.; Gonçalves, Amanda G.; Silva, Marcio R.; Hungaro, Humberto M. (2018), "Campylobacter : An Important Food Safety Issue", Food Safety and Preservation, Elsevier, pp. 391–430, doi:10.1016/b978-0-12-814956-0.00013-5, ISBN 978-0-12-814956-0, retrieved 2024-04-16
  3. ^ a b c d Macuch, P.J.; Tanner, A.C.R. (2000-02). "Campylobacter Species in Health, Gingivitis, and Periodontitis". Journal of Dental Research. 79 (2): 785–792. doi:10.1177/00220345000790021301. ISSN 0022-0345. {{cite journal}}: Check date values in: |date= (help)
  4. ^ a b c d e f g h i j Hsu, Tiffany; Gemmell, Matthew R.; Franzosa, Eric A.; Berry, Susan; Mukhopadhya, Indrani; Hansen, Richard; Michaud, Monia; Nielsen, Hans; Miller, William G.; Nielsen, Henrik; Bajaj-Elliott, Mona; Huttenhower, Curtis; Garrett, Wendy S.; Hold, Georgina L. (2019). "Comparative genomics and genome biology of Campylobacter showae". Emerging Microbes & Infections. 8 (1): 827–840. doi:10.1080/22221751.2019.1622455. ISSN 2222-1751. PMC 6567213. PMID 31169073.{{cite journal}}: CS1 maint: PMC format (link)
  5. ^ Zhong, Chaofang; Qu, Bingpeng; Hu, Gang; Ning, Kang (2022-10-26). Garcia-Solache, Monica Adriana (ed.). "Pan-Genome Analysis of Campylobacter: Insights on the Genomic Diversity and Virulence Profile". Microbiology Spectrum. 10 (5). doi:10.1128/spectrum.01029-22. ISSN 2165-0497. PMC 9602946. PMID 36069574.{{cite journal}}: CS1 maint: PMC format (link)
  6. ^ Warren, René L; Freeman, Douglas J; Pleasance, Stephen; Watson, Peter; Moore, Richard A; Cochrane, Kyla; Allen-Vercoe, Emma; Holt, Robert A (2013-12). "Co-occurrence of anaerobic bacteria in colorectal carcinomas". Microbiome. 1 (1). doi:10.1186/2049-2618-1-16. ISSN 2049-2618. PMC 3971631. PMID 24450771. {{cite journal}}: Check date values in: |date= (help)CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)

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