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| __NOTOC__
| | #REDIRECT [[Yersinia pestis]] |
| {{Yersinia pestis infection}}
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| {{CMG}}; Assistant Editors-In-Chief: Esther Lee, M.A.; {{Rim}}
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| ==Overview==
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| ''[[Yersinia pestis]]'' (''Y. pestis''), a rod-shaped [[facultative anaerobe]] with bipolar staining (giving it a safety pin appearance) causes the infection in mammals and humans.<ref name=Baron>{{cite book | author = Collins FM | title = Pasteurella, Yersinia, and Francisella. ''In:'' Baron's Medical Microbiology ''(Baron S ''et al'', eds.)| edition = 4th | publisher = Univ. of Texas Medical Branch | year = 1996 | url = http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=mmed.section.1611 | isbn = 0-9631172-1-1 }}</ref> The bacteria maintain their existence in a cycle involving rodents and their fleas. The genus Yersinia is [[gram-negative]], bipolar staining coccobacilli, and, similarly to other [[Enterobacteriaceae]], it has a fermentative metabolism. ''Y. pestis'' produces an antiphagocytic slime. The organism is motile when isolated, but becomes nonmotile in the mammalian host.
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| ==Taxonomy==
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| [[Bacteria]]; [[Proteobacteria]]; [[Proteobacteria#Gammaproteobacteria|Gammaproteobacteria]]; [[Enterobacteriales]]; ''[[Yersinia]]''; [[Yersinia pestis]]
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| ==Biology==
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| Yersinia pests is a nonmotile, non-spore-forming, Gram-negative, non-lactose fermenting, bipolar, ovoid, "safety-pin-shaped" bacillus.
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| ===Genome===
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| The complete [[genome|genomic]] sequence is available for two of the three sub-species of yersinia pestis: strain KIM (of biovar Medievalis),<ref>{{cite journal | author = Deng W| title = Genome Sequence of Yersinia pestis KIM | journal = Journal of Bacteriology | year = 2002 | volume = 184 | issue = 16 | pages = 4601–4611 | doi= 10.1128/JB.184.16.4601-4611.2002 | pmid=12142430 | pmc = 135232 | author-separator = , | display-authors = 1 | last2 = Burland | first2 = V. | last3 = Plunkett Iii | first3 = G. | last4 = Boutin | first4 = A. | last5 = Mayhew | first5 = G. F. | last6 = Liss | first6 = P. | last7 = Perna | first7 = N. T. | last8 = Rose | first8 = D. J. | last9 = Mau | first9 = B.}}</ref> and strain CO92 (of biovar Orientalis, obtained from a clinical isolate in the United States).<ref>{{cite journal | author = Parkhill J| title = Genome sequence of Yersinia pestis, the causative agent of plague | journal = Nature | year = 2001 | volume = 413 | issue = 6855| pages = 523–527 | doi = 10.1038/35097083 | pmid = 11586360 | author-separator = , | display-authors = 1 | last2 = Wren | first2 = B. W. | last3 = Thomson | first3 = N. R. | last4 = Titball | first4 = R. W. | last5 = Holden | first5 = M. T. G. | last6 = Prentice | first6 = M. B. | last7 = Sebaihia | first7 = M. | last8 = James | first8 = K. D. | last9 = Churcher | first9 = C.}}</ref> As of 2006, the genomic sequence of a strain of biovar Antiqua has been recently completed.<ref name="pmid16740952">{{cite journal |author=Chain PS |title=Complete Genome Sequence of Yersinia pestis Strains Antiqua and Nepal516: Evidence of Gene Reduction in an Emerging Pathogen |journal=J. Bacteriol. |volume=188 |issue=12 |pages=4453–63 |year=2006 |pmid=16740952 |doi=10.1128/JB.00124-06 |pmc=1482938 |author-separator=, |author2=Hu P |author3=Malfatti SA |display-authors=3 |last4=Radnedge |first4=L. |last5=Larimer |first5=F. |last6=Vergez |first6=L. M. |last7=Worsham |first7=P. |last8=Chu |first8=M. C. |last9=Andersen |first9=G. L.}}</ref> Similar to the other pathogenic strains, there are signs of loss of function mutations. The [[chromosome]] of strain KIM is 4,600,755 base pairs long; the chromosome of strain CO92 is 4,653,728 base pairs long. Like its cousins [[Yersinia pseudotuberculosis|Yersinia pseudotuberculosis]] and [[Yersinia enterocolitica|Yersinia enterocolitica]], Yersinia pestis is host to the [[plasmid]] pCD1. In addition, it also hosts two other plasmids, pPCP1 (also called pPla or pPst) and pMT1 (also called pFra) that are not carried by the other Yersinia species. pFra codes for a [[phospholipase D]] that is important for the ability of Yersinia pestis to be transmitted by fleas. pPla codes for a [[protease]], Pla, that activates [[plasminogen]] in human hosts and is a very important [[virulence factor]] for pneumonic plague.<ref name="pmid17255510">{{cite journal| author=Lathem WW, Price PA, Miller VL, Goldman WE| title=A plasminogen-activating protease specifically controls the development of primary pneumonic plague. | journal=Science | year= 2007 | volume= 315 | issue= 5811 | pages= 509-13 | pmid=17255510 | doi=10.1126/science.1137195 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17255510 }} </ref> Together, these plasmids, and a [[pathogenicity island]] called HPI, encode several proteins that cause the pathogenesis, for which Yersinia pestis is famous. Among other things, these [[virulence]] factors are required for bacterial adhesion and injection of proteins into the host cell, invasion of bacteria in the host cell (via a Type III secretion system), and acquisition and binding of iron that is harvested from red blood cells (via siderophores). Yersinia pestis is thought to be descendant from Yersinia pseudotuberculosis, differing only in the presence of specific virulence plasmids.
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| A comprehensive and comparative [[proteomics]] analysis of Yersinia pestis strain KIM was performed in 2006.<ref>{{cite journal | author = Hixson K| title = Biomarker candidate identification in Yersinia pestis using organism-wide semiquantitative proteomics | journal = Journal of Proteome Research | year = 2006 | volume = 5 | issue = 11 | pages = 3008–3017 | pmid = 16684765 | doi = 10.1021/pr060179y | author-separator = , | display-authors = 1 | last2 = Adkins | first2 = Joshua N. | last3 = Baker | first3 = Scott E. | last4 = Moore | first4 = Ronald J. | last5 = Chromy | first5 = Brett A. | last6 = Smith | first6 = Richard D. | last7 = McCutchen-Maloney | first7 = Sandra L. | last8 = Lipton | first8 = Mary S. | last9 = Heffron | first9 = F}}</ref> The analysis focused on the transition to a growth condition mimicking growth in host cells.
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| ==Tropism==
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| ==Natural reservoir==
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| ==References==
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| {{Reflist|2}}
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| [[Category:Dermatology]]
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| [[Category:Infectious disease]]
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| [[Category:Pulmonology]]
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| [[Category:Hematology]]
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| [[Category:Disease]]
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| {{WH}}
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| {{WS}}
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