Salmonella enterica subsp. enterica: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
added paragraphs containing information on survival in the stomach of salmonelle enterica subsp.enterica and also the iron uptake and metabolism.
Tags: Reverted nowiki added Visual edit
Citation bot (talk | contribs)
Altered pmc. Add: jstor, page, authors 1-1. Removed URL that duplicated identifier. Removed parameters. Some additions/deletions were parameter name changes. | Use this bot. Report bugs. | Suggested by Jay8g | Category:CS1 maint: PMC format | #UCB_Category 4/6
 
(31 intermediate revisions by 18 users not shown)
Line 31: Line 31:
A number of techniques are currently used to differentiate between [[serotype]]s. These include looking for the presence or absence of [[antigen]]s, [[phage typing]], molecular fingerprinting and biotyping, where serovars are differentiated by which nutrients they are able to ferment. A possible factor in determining the host range of particular serovars is phage-mediated acquisition of a small number of genetic elements that enable infection of a particular host.<ref>{{cite journal | vauthors = Rabsch W, Andrews HL, Kingsley RA, Prager R, Tschäpe H, Adams LG, Bäumler AJ | title = Salmonella enterica serotype Typhimurium and its host-adapted variants | journal = Infection and Immunity | volume = 70 | issue = 5 | pages = 2249–2255 | date = May 2002 | pmid = 11953356 | pmc = 127920 | doi = 10.1128/IAI.70.5.2249-2255.2002 }}</ref> It is further postulated that serovars which infect a narrow range of species have diverged from ancestors with a broad host range, and have since specialised and lost the ability to infect some hosts.<ref>{{cite journal | vauthors = Langridge GC, Fookes M, Connor TR, Feltwell T, Feasey N, Parsons BN, Seth-Smith HM, Barquist L, Stedman A, Humphrey T, Wigley P, Peters SE, Maskell DJ, Corander J, Chabalgoity JA, Barrow P, Parkhill J, Dougan G, Thomson NR | display-authors = 6 | title = Patterns of genome evolution that have accompanied host adaptation in Salmonella | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 112 | issue = 3 | pages = 863–868 | date = January 2015 | pmid = 25535353 | pmc = 4311825 | doi = 10.1073/pnas.1416707112 | author13-link = Duncan Maskell | doi-access = free | bibcode = 2015PNAS..112..863L }}</ref>
A number of techniques are currently used to differentiate between [[serotype]]s. These include looking for the presence or absence of [[antigen]]s, [[phage typing]], molecular fingerprinting and biotyping, where serovars are differentiated by which nutrients they are able to ferment. A possible factor in determining the host range of particular serovars is phage-mediated acquisition of a small number of genetic elements that enable infection of a particular host.<ref>{{cite journal | vauthors = Rabsch W, Andrews HL, Kingsley RA, Prager R, Tschäpe H, Adams LG, Bäumler AJ | title = Salmonella enterica serotype Typhimurium and its host-adapted variants | journal = Infection and Immunity | volume = 70 | issue = 5 | pages = 2249–2255 | date = May 2002 | pmid = 11953356 | pmc = 127920 | doi = 10.1128/IAI.70.5.2249-2255.2002 }}</ref> It is further postulated that serovars which infect a narrow range of species have diverged from ancestors with a broad host range, and have since specialised and lost the ability to infect some hosts.<ref>{{cite journal | vauthors = Langridge GC, Fookes M, Connor TR, Feltwell T, Feasey N, Parsons BN, Seth-Smith HM, Barquist L, Stedman A, Humphrey T, Wigley P, Peters SE, Maskell DJ, Corander J, Chabalgoity JA, Barrow P, Parkhill J, Dougan G, Thomson NR | display-authors = 6 | title = Patterns of genome evolution that have accompanied host adaptation in Salmonella | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 112 | issue = 3 | pages = 863–868 | date = January 2015 | pmid = 25535353 | pmc = 4311825 | doi = 10.1073/pnas.1416707112 | author13-link = Duncan Maskell | doi-access = free | bibcode = 2015PNAS..112..863L }}</ref>


The CDC publishes a ''Salmonella'' Annual Report with a list of serovars most commonly associated with human illness, the top 10 serovars are listed below:<ref>{{Cite web |date=2016 |title=National Enteric Disease Surveillance: Salmonella Annual Report, 2016 |url=https://www.cdc.gov/nationalsurveillance/pdfs/2016-Salmonella-report-508.pdf |website=CDC.gov}}</ref>
The [[Centers for Disease Control and Prevention|CDC]] publishes a ''Salmonella'' Annual Report with a list of serovars most commonly associated with human illness, the top 10 serovars are listed below:<ref>{{Cite web |date=2016 |title=National Enteric Disease Surveillance: Salmonella Annual Report, 2016 |url=https://www.cdc.gov/nationalsurveillance/pdfs/2016-Salmonella-report-508.pdf |website=CDC.gov}}</ref>
{| class="wikitable"
{| class="wikitable"
|Rank
!Rank
|Serotype
!Serotype
|Percent
!Percent
|-
|-
|1
|1
Line 81: Line 81:
|41.5
|41.5
|}
|}
Studies have concluded most strains of ''Salmonella enterica'' subsp. ''enterica'' serovars possess serotype-specific virulence plasmids. These are plasmid-associated virulence characterized by low-copy-number plasmids and depending on the serovar, its size ranges from 50 to 100 kb.<ref>{{cite journal | vauthors = Rotger R, Casadesús J | title = The virulence plasmids of Salmonella | journal = International Microbiology | volume = 2 | issue = 3 | pages = 177–184 | date = September 1999 | pmid = 10943411 | url = https://core.ac.uk/download/pdf/159083976.pdf }}</ref> Serovar Enteritidis, which is the most common serovar isolated in human clinical cases, has also been found to produce endotoxins, coded by the ''stn'' and ''sly''A genes, that attribute to the pathogenicity of Enteritidis.<ref>{{cite journal | vauthors = Ashkenazi S, Cleary TG, Murray BE, Wanger A, Pickering LK | title = Quantitative analysis and partial characterization of cytotoxin production by Salmonella strains | journal = Infection and Immunity | volume = 56 | issue = 12 | pages = 3089–3094 | date = December 1988 | doi = 10.1128/iai.56.12.3089-3094.1988 | pmid = 3182072 | pmc = 259706 }}</ref>
Studies have concluded most strains of ''Salmonella enterica'' subsp. ''enterica'' serovars possess serotype-specific virulence [[plasmid]]s. These are plasmid-associated virulence characterized by low-copy-number plasmids and depending on the serovar, its size ranges from 50 to 100 kb.<ref>{{cite journal | vauthors = Rotger R, Casadesús J | title = The virulence plasmids of Salmonella | journal = International Microbiology | volume = 2 | issue = 3 | pages = 177–184 | date = September 1999 | pmid = 10943411 | url = https://core.ac.uk/download/pdf/159083976.pdf }}</ref> In 2012, CDC's [[PulseNet]] became aware of a emergent multi-drug resistant Serovar Infantis [[SNP genotyping|SNP]] cluster, named REPJFX01. This SNP cluster has a large megaplasmid (pESI) that contains multiple drug-resistance genes.<ref>{{Cite web |last=CDC |date=2023-07-21 |title=Persistent Strain of Salmonella Infantis (REPJFX01) Linked to Chicken |url=https://www.cdc.gov/ncezid/dfwed/outbreak-response/rep-strains/repjfx01.html |access-date=2023-11-19 |website=Centers for Disease Control and Prevention |language=en-us}}</ref> The USDA NARMS stated that because of this pESI-plasmid, serovar Infantis is the leading serovar in poultry.<ref>{{Cite web |date=2023-02-10 |title=FSIS NARMS Multi-Year Report – 2014-2019 |url=https://www.fsis.usda.gov/news-events/publications/fsis-narms-multi-year-report-2014-2019 |access-date=2023-11-15 |website=fsis.usda.gov}}</ref> [[National Center for Biotechnology Information|NCBI]] has over 12,500 isolates in the REPJFX01 SNP cluster, with over 3,700 being clinical isolates.<ref>{{Cite web |title=Isolates Browser - Pathogen Detection - NCBI |url=https://www.ncbi.nlm.nih.gov/pathogens/isolates/#PNUSAS212095 |access-date=2023-11-19 |website=ncbi.nlm.nih.gov}}</ref> Serovar Enteritidis, which is the most common serovar isolated in human clinical cases, has also been found to produce [[endotoxins]], coded by the ''stn'' and ''sly''A genes, that attribute to the pathogenicity of Enteritidis.<ref>{{cite journal | vauthors = Ashkenazi S, Cleary TG, Murray BE, Wanger A, Pickering LK | title = Quantitative analysis and partial characterization of cytotoxin production by Salmonella strains | journal = Infection and Immunity | volume = 56 | issue = 12 | pages = 3089–3094 | date = December 1988 | doi = 10.1128/iai.56.12.3089-3094.1988 | pmid = 3182072 | pmc = 259706 }}</ref> Salmonella typhimurium notoriously known as the causative agent for typhoid can be used to deliver various cancer therapies. Tumors with their immune-suppressive microenvironments allow 1000 fold greater localization of engineered S. typhimurium than healthy tissues which are then able to enter tumor cells, lyse and deliver therapies.<ref>{{Cite journal |last1=Raman |first1=Vishnu |last2=Van Dessel |first2=Nele |last3=Hall |first3=Christopher L. |last4=Wetherby |first4=Victoria E. |last5=Whitney |first5=Samantha A. |last6=Kolewe |first6=Emily L. |last7=Bloom |first7=Shoshana M. K. |last8=Sharma |first8=Abhinav |last9=Hardy |first9=Jeanne A. |last10=Bollen |first10=Mathieu |last11=Van Eynde |first11=Aleyde |last12=Forbes |first12=Neil S. |date=2021-10-21 |title=Intracellular delivery of protein drugs with an autonomously lysing bacterial system reduces tumor growth and metastases |journal=Nature Communications |language=en |volume=12 |issue=1 |page=6116 |doi=10.1038/s41467-021-26367-9 |issn=2041-1723 |pmc=8531320 |pmid=34675204}}</ref>


In November 2016, a new strain of extensively drug resistant (XDR) ''Salmonella enterica'' serovar Typhi emerged in Pakistan, primarily from the cities of [[Hyderabad, Sindh|Hyderabad]] and [[Karachi]].<ref>{{Cite web | vauthors = Daley J | date = 21 February 2018 |url=https://www.the-scientist.com/the-nutshell/typhoid-outbreak-in-pakistan-linked-to-extensively-drug-resistant-bacteria-30090|title=Typhoid Outbreak in Pakistan Linked to Extensively Drug-Resistant Bacteria|website=The Scientist Magazine®|language=en|access-date=2018-09-03}}</ref> [[Multiple drug resistance|Multidrug resistant]] strains have been present since the late 1970s in Africa and Asia.<ref>{{cite journal | vauthors = Klemm EJ, Shakoor S, Page AJ, Qamar FN, Judge K, Saeed DK, Wong VK, Dallman TJ, Nair S, Baker S, Shaheen G, Qureshi S, Yousafzai MT, Saleem MK, Hasan Z, Dougan G, Hasan R | display-authors = 6 | title = Emergence of an Extensively Drug-Resistant <i>Salmonella enterica</i> Serovar Typhi Clone Harboring a Promiscuous Plasmid Encoding Resistance to Fluoroquinolones and Third-Generation Cephalosporins | journal = mBio | volume = 9 | issue = 1 | date = February 2018 | pmid = 29463654 | pmc = 5821095 | doi = 10.1128/mBio.00105-18 }}</ref> These XDR strains are resistant to all antibiotic treatment options: [[chloramphenicol]], [[ampicillin]], [[trimethoprim-sulfamethoxazole]], [[fluoroquinolones]], and [[third-generation cephalosporins]]. The outbreak has been ongoing since 2016.<ref>{{Cite web|url=https://wwwnc.cdc.gov/travel/notices/alert/xdr-typhoid-fever-pakistan|title=Extensively Drug-Resistant Typhoid Fever in Pakistan – Alert – Level 2, Practice Enhanced Precautions | work = Travel Health Notices | publisher = U.S. Centers for Disease Control and Prevention |language=en-us|access-date=2018-09-03}}</ref>
In November 2016, a new strain of extensively drug resistant (XDR) ''Salmonella enterica'' serovar Typhi emerged in Pakistan, primarily from the cities of [[Hyderabad, Sindh|Hyderabad]] and [[Karachi]].<ref>{{Cite web | vauthors = Daley J | date = 21 February 2018 |url=https://www.the-scientist.com/the-nutshell/typhoid-outbreak-in-pakistan-linked-to-extensively-drug-resistant-bacteria-30090|title=Typhoid Outbreak in Pakistan Linked to Extensively Drug-Resistant Bacteria|website=The Scientist Magazine®|language=en|access-date=2018-09-03}}</ref> [[Multiple drug resistance|Multidrug resistant]] strains have been present since the late 1970s in Africa and Asia.<ref>{{cite journal | vauthors = Klemm EJ, Shakoor S, Page AJ, Qamar FN, Judge K, Saeed DK, Wong VK, Dallman TJ, Nair S, Baker S, Shaheen G, Qureshi S, Yousafzai MT, Saleem MK, Hasan Z, Dougan G, Hasan R | display-authors = 6 | title = Emergence of an Extensively Drug-Resistant ''Salmonella enterica'' Serovar Typhi Clone Harboring a Promiscuous Plasmid Encoding Resistance to Fluoroquinolones and Third-Generation Cephalosporins | journal = mBio | volume = 9 | issue = 1 | date = February 2018 | pmid = 29463654 | pmc = 5821095 | doi = 10.1128/mBio.00105-18 }}</ref> These XDR strains are resistant to all antibiotic treatment options: [[chloramphenicol]], [[ampicillin]], [[trimethoprim-sulfamethoxazole]], [[fluoroquinolones]], and [[third-generation cephalosporins]]. The outbreak has been ongoing since 2016.<ref>{{Cite web|url=https://wwwnc.cdc.gov/travel/notices/alert/xdr-typhoid-fever-pakistan|title=Extensively Drug-Resistant Typhoid Fever in Pakistan – Alert – Level 2, Practice Enhanced Precautions | work = Travel Health Notices | publisher = U.S. Centers for Disease Control and Prevention |language=en-us|access-date=2018-09-03}}</ref>

== Iron Uptake and Metabolism ==
Serovars of the genus ''Salmonella'' bonded with lower molecular weight compounds called siderophores<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. Sensitivity growth stimulation bioassays were performed to examine the transport of a group of siderophores and the ferroxamines. The uptake of all three ferrioxamines showed to be dependent on the transport across the outer membrane through the FoxA protein<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. Transport across the inner membrane of this group of ferrioxamines showed to be dependent on the periplasmic binding protein-dependent inner membrane ABC transporter<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. The FoxA receptor gene distribution was determined by DNA hybridization and was limited to ''Salmonella Enterica subsp''. ''Salmonella Enterica'' serovar typhimurium strains were unable to utilize certain groups of the ferrioxamines as a sole source of iron<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. ''AS.Enterica'' serovar typhimurium strain that contained an insertion of TnphoA into the gene encodes the periplasmic binding protein element of the inner membrane transport system was unable to utilize high iron limitation<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>.

== Survival in the Stomach ==
Under normal circumstances, ''Salmonella enterica'' infections range from 10^6 and 10^7 bacilli<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. There are certain scenarios that can occur to decrease the infection risk<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. These include, a higher pH in the stomach, gastric resection, and treatment with anti acid buffering<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>. It is important to note that if the stomach has a lower pH, then this helps as a defensive technique to potentially fight off this infection<ref>Kingsley, Robert Anthony. ''Iron Uptake and Metabolism by Salmonella Enterica''. Jan. 1997. ''EBSCOhost'', search.ebscohost.com/login.aspx?direct=true&AuthType=ip,shib&db=edsble&AN=edsble.696232&site=eds-live.</ref>.

''Salmonella Enterica subsp. enterica'' virulence potential can be linked to higher survival within work that is performed outside a living organism from a human gastrointestinal model. "Food Microbiology" evaluated whether ''Salmonella'' virulence could potentially be linked to a greater ability to survive consecutive digestive environments<ref>Cavestri, C., Savard, P., Fliss, I., Emond-Rhéault, J. G., Hamel, J., Kukavica-Ibrulj, I., Boyle, B., Daigle, F., Malo, D., Bekal, S., Harris, L. J., Levesque, R. C., Goodridge, L., & Lapointe, G. (2021). Salmonella enterica subsp. enterica virulence potential can be linked to higher survival within a dynamic in vitro human gastrointestinal model. ''Food Microbiology'', ''101''. <nowiki>https://doi.org/https://www.sciencedirect.com/science/article/pii/S0740002021001428</nowiki></ref>. 13 different strains of S.enterica were selected based upon their high and low virulence phenotypes that were obtained from Dr. Daigle's Labratory<ref>Crouse, A., Schramm, C., Emond, J.-G., Herod, A., Kerhoas, M., Rohde, J., Gruenheid, S., Greenwood, C., Goodridge, L.D., Garduno, R., Levesque, R.C., Malo, D., Daigle, F., 2020. Combining whole genome sequencing and multi-model phenotyping to identify genetic predictors of Salmonella virulence. mSphere 5. <nowiki>https://doi.org/</nowiki> 10.1128/mSphere .00293-20 e00293-20.</ref>. Testing included using lettuce as a food source for the strains to examine the passage through the stomach<ref>Ribnicky, D.M., Roopchand, D.E., Oren, A., Grace, M., Poulev, A., Lila, M.A., Havenaar, R., Raskin, I., 2014. Effects of a high fat meal matrix and protein complexation on the bioaccessibility of blueberry anthocyanins using the TNO gastrointestinal model (TIM-1). Food Chem. 142, 349–357. <nowiki>https://doi.org/</nowiki> 10.1016/j.foodchem.2013.07.073.</ref>. After passage, both virulence phenotype strains survived but only the high virulence strain had a greater survival rate<ref>Cavestri, C., Savard, P., Fliss, I., Emond-Rhéault, J. G., Hamel, J., Kukavica-Ibrulj, I., Boyle, B., Daigle, F., Malo, D., Bekal, S., Harris, L. J., Levesque, R. C., Goodridge, L., & Lapointe, G. (2021). Salmonella enterica subsp. enterica virulence potential can be linked to higher survival within a dynamic in vitro human gastrointestinal model. ''Food Microbiology'', ''101''. <nowiki>https://doi.org/https://www.sciencedirect.com/science/article/pii/S0740002021001428</nowiki></ref>. These survival rates could be linked to acid and bile resistant genes that are present. Certain capacities within S.enterica that survive in the human digestion tract have a low pH of the stomach and enzymatic secretions that overall affect the virulence<ref>Alvarez-Ord ´ o´nez, ˜ A., Begley, M., Prieto, M., Messens, W., Lopez, ´ M., Bernardo, A., Hill, C., 2011. Salmonella spp. survival strategies within the host gastrointestinal tract. Microbiology 157, 3268–3281. <nowiki>https://doi.org/10.1099/mic.0.050351-0</nowiki></ref>.


==Nomenclature==
==Nomenclature==
The nomenclature of ''Salmonella enterica'' has long been a topic of debate in the microbiology community.<ref>{{cite journal | vauthors = Su LH, Chiu CH | title = Salmonella: clinical importance and evolution of nomenclature | journal = Chang Gung Medical Journal | volume = 30 | issue = 3 | pages = 210–219 | date = 2007 | pmid = 17760271 | url = http://cgmj.cgu.edu.tw/3003/300302.pdf }}</ref> Originally in the 1880s, ''Salmonella'' species were named after the disease, host, or geological location they were associated with; however, this taxonomic characterization was contested due to genus members being categorized incompatibly with their genetic similarities. In the 1980s, the emergence of nucleotide sequencing and DNA hybridization led many established bacteriologists such as Le Minor and Popoff (1987), Euzéby (1999), and Ezaki and Yabuuchi (2000) to put forth their proposals for nomenclature changes.<ref>{{cite journal | vauthors = Agbaje M, Begum RH, Oyekunle MA, Ojo OE, Adenubi OT | title = Evolution of Salmonella nomenclature: a critical note | journal = Folia Microbiologica | volume = 56 | issue = 6 | pages = 497–503 | date = November 2011 | pmid = 22052214 | doi = 10.1007/s12223-011-0075-4 | s2cid = 19799923 }}</ref> It was not until 2005, that Le Minor and Popoff reproposed and established that "''Salmonella enterica''" would be the approved species name –excluding ''Salmonella bongori''– and that ''Salmonella enterica'' contains six subspecies, of which, ''Salmonella enterica'' subsp. ''enterica'' contains the most serovars.<ref>{{cite journal | vauthors = Brenner FW, Villar RG, Angulo FJ, Tauxe R, Swaminathan B | title = Salmonella nomenclature | journal = Journal of Clinical Microbiology | volume = 38 | issue = 7 | pages = 2465–2467 | date = July 2000 | pmid = 10878026 | pmc = 86943 | doi = 10.1128/JCM.38.7.2465-2467.2000 }}</ref> Technological advancements allow researchers to use whole genome sequencing data to identify and group serovars using two methods: sequence typing and antigen recognition<ref>{{cite journal | vauthors = Chattaway MA, Langridge GC, Wain J | title = Salmonella nomenclature in the genomic era: a time for change | journal = Scientific Reports | volume = 11 | issue = 1 | pages = 7494 | date = April 2021 | pmid = 33820940 | pmc = 8021552 | doi = 10.1038/s41598-021-86243-w | bibcode = 2021NatSR..11.7494C }}</ref>.
The nomenclature of ''Salmonella enterica'' has long been a topic of debate in the microbiology community.<ref>{{cite journal | vauthors = Su LH, Chiu CH | title = Salmonella: clinical importance and evolution of nomenclature | journal = Chang Gung Medical Journal | volume = 30 | issue = 3 | pages = 210–219 | date = 2007 | pmid = 17760271 | url = http://cgmj.cgu.edu.tw/3003/300302.pdf }}</ref> Originally in the 1880s, ''Salmonella'' species were named after the disease, host, or geological location they were associated with; however, this taxonomic characterization was contested due to genus members being categorized incompatibly with their genetic similarities. In the 1980s, the emergence of nucleotide sequencing and DNA hybridization led many established bacteriologists such as Le Minor and Popoff (1987), Euzéby (1999), and Ezaki and Yabuuchi (2000) to put forth their proposals for nomenclature changes.<ref>{{cite journal | vauthors = Agbaje M, Begum RH, Oyekunle MA, Ojo OE, Adenubi OT | title = Evolution of Salmonella nomenclature: a critical note | journal = Folia Microbiologica | volume = 56 | issue = 6 | pages = 497–503 | date = November 2011 | pmid = 22052214 | doi = 10.1007/s12223-011-0075-4 | s2cid = 19799923 }}</ref> It was not until 2005, that Le Minor and Popoff reproposed and established that "''Salmonella enterica''" would be the approved species name – excluding ''Salmonella bongori'' – and that ''Salmonella enterica'' contains six subspecies, of which ''Salmonella enterica'' subsp. ''enterica'' contains the most serovars.<ref>{{cite journal | vauthors = Brenner FW, Villar RG, Angulo FJ, Tauxe R, Swaminathan B | title = Salmonella nomenclature | journal = Journal of Clinical Microbiology | volume = 38 | issue = 7 | pages = 2465–2467 | date = July 2000 | pmid = 10878026 | pmc = 86943 | doi = 10.1128/JCM.38.7.2465-2467.2000 }}</ref> Technological advancements allow researchers to use whole genome sequencing data to identify and group serovars using two methods: sequence typing and antigen recognition.<ref>{{cite journal | vauthors = Chattaway MA, Langridge GC, Wain J | title = Salmonella nomenclature in the genomic era: a time for change | journal = Scientific Reports | volume = 11 | issue = 1 | pages = 7494 | date = April 2021 | pmid = 33820940 | pmc = 8021552 | doi = 10.1038/s41598-021-86243-w | bibcode = 2021NatSR..11.7494C }}</ref>


Serovar names are capitalized but not italicized or underlined. Serovars may be designated in full form or short form (includes just the genus and serovar names). For example, in full designation ''Salmonella enterica'' subsp. ''enterica'' serovar Typhi is written as such, but in short designation it is written as Salmonella Typhi.<ref>{{cite web |title=Scientific Nomenclature |url=https://wwwnc.cdc.gov/eid/page/scientific-nomenclature |access-date=17 February 2020 |website=Emerging Infectious Dieases |publisher=Centers for Disease Control and Prevention}}</ref> Each serovar can have many strains, as well, which allows for a rapid increase in the total number of [[Antigenic variation|antigenically variable]] bacteria.<ref>{{Cite web |title=Salmonella spp. comparative sequencing | work = Wellcome Trust Genome Campus |url= https://web.archive.org/web/20071114165837/http://www.sanger.ac.uk/Projects/Salmonella/ |archive-url=https://www.sanger.ac.uk/Projects/Salmonella/ |archive-date=2007-11-14}}</ref>
Serovar names are capitalized but not italicized or underlined. Serovars may be designated in full form or short form (includes just the genus and serovar names). For example, in full designation ''Salmonella enterica'' subsp. ''enterica'' serovar Typhi is written as such, but in short designation it is written as ''Salmonella'' Typhi.<ref>{{cite web |title=Scientific Nomenclature |url=https://wwwnc.cdc.gov/eid/page/scientific-nomenclature |access-date=17 February 2020 |website=Emerging Infectious Dieases |publisher=Centers for Disease Control and Prevention}}</ref> Each serovar can have many strains, as well, which allows for a rapid increase in the total number of [[Antigenic variation|antigenically variable]] bacteria.<ref>{{Cite web |title=Salmonella spp. comparative sequencing | work = Wellcome Trust Genome Campus |url= https://web.archive.org/web/20071114165837/http://www.sanger.ac.uk/Projects/Salmonella/ |archive-url=https://www.sanger.ac.uk/Projects/Salmonella/ |archive-date=2007-11-14}}</ref>


== Epidemiology ==
== Epidemiology ==
{{main|Salmonellosis}}
{{main|Salmonellosis}}


The World Health Organization characterizes salmonellosis as a foodborne disease whose symptoms include diarrhea, fever, nausea, vomiting, and in severe cases death<ref>{{Cite web |title=Salmonella (non-typhoidal) |url=https://www.who.int/news-room/fact-sheets/detail/salmonella-(non-typhoidal) |access-date=2023-10-26 |website=www.who.int |language=en}}</ref>. Salmonellosis has been assessed to primarily occur in human hosts due to bacterial colonization of the intestinal track after the consumption of contaminated food or water, but it is also known to spread from person-to-person to via the fecal-oral-route<ref>{{Citation |last=Giannella |first=Ralph A. |title=Salmonella |date=1996 |url=http://www.ncbi.nlm.nih.gov/books/NBK8435/ |work=Medical Microbiology |editor-last=Baron |editor-first=Samuel |access-date=2023-10-26 |edition=4th |place=Galveston (TX) |publisher=University of Texas Medical Branch at Galveston |isbn=978-0-9631172-1-2 |pmid=21413334}}</ref>. To reduce the risk associated with contracting this disease, proper food safety measures should be applied to high-risk food products including poultry, beef, pork, lamb, eggs, and fresh produce<ref name=":0">Ehuwa O, Jaiswal AK, Jaiswal S. Salmonella, food safety and food handling practices. ''Foods''. 2021;10(5). doi:<nowiki>https://www.mdpi.com/2304-8158/10/5/907/htm</nowiki></ref>. Food manufacturers, ingredient suppliers, restaurants, and home cooks should practice sanitary processing procedures, store foods below 41 degrees Celsius, and thoroughly cook all foods to their designated safe-to-eat temperatures<ref name=":0" />.It has become increasingly difficult to mitigate the presence of salmonellosis infections across the human population due to the unique nature of multidrug-resistant serovars as a result of the counterproductive effects to use antibiotics as a broad spectrum treatment<ref>https://www.nejm.org/doi/full/10.1056/NEJM199805073381901</ref>. Key host [[immune deficiencies]] associated with [[HIV]], [[malaria]] and malnutrition have contributed to a wide spread of this disease and the need to use expensive [[antimicrobial drugs]] in the poorest health services in the world.<ref>{{cite journal |vauthors=Feasey NA, Dougan G, Kingsley RA, Heyderman RS, Gordon MA |date=June 2012 |title=Invasive non-typhoidal salmonella disease: an emerging and neglected tropical disease in Africa |journal=Lancet |volume=379 |issue=9835 |pages=2489–2499 |doi=10.1016/s0140-6736(11)61752-2 |pmc=3402672 |pmid=22587967}}</ref> But also bacterial factors, such as upregulated activity of the virulence gene ''pgtE'', due to a [[Single-nucleotide polymorphism|single nucleotide polymorphism]] (SNP) in its promoter region, have been shown to have a great impact upon the pathogenesis of this particular ''Salmonella'' sequence type.<ref>{{cite journal |display-authors=6 |vauthors=Hammarlöf DL, Kröger C, Owen SV, Canals R, Lacharme-Lora L, Wenner N, Schager AE, Wells TJ, Henderson IR, Wigley P, Hokamp K, Feasey NA, Gordon MA, Hinton JC |date=March 2018 |title=Role of a single noncoding nucleotide in the evolution of an epidemic African clade of <i>Salmonella</i> |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=115 |issue=11 |pages=E2614–E2623 |bibcode=2018PNAS..115E2614H |doi=10.1073/pnas.1714718115 |pmc=5856525 |pmid=29487214 |doi-access=free}}</ref>
The World Health Organization characterizes [[salmonellosis]] as a foodborne disease whose symptoms include diarrhea, fever, nausea, vomiting, and in severe cases death.<ref>{{Cite web |title=Salmonella (non-typhoidal) |url=https://www.who.int/news-room/fact-sheets/detail/salmonella-(non-typhoidal) |access-date=2023-10-26 |website=www.who.int |language=en}}</ref> [[Salmonellosis]] has been assessed to primarily occur in human hosts due to bacterial colonization of the intestinal tract after the consumption of contaminated food or water, but it is also known to spread from person-to-person via the fecal-oral route.<ref>{{Citation |last=Giannella |first=Ralph A. |title=Salmonella |date=1996 |url=http://www.ncbi.nlm.nih.gov/books/NBK8435/ |work=Medical Microbiology |editor-last=Baron |editor-first=Samuel |access-date=2023-10-26 |edition=4th |place=Galveston (TX) |publisher=University of Texas Medical Branch at Galveston |isbn=978-0-9631172-1-2 |pmid=21413334}}</ref> To reduce the risk associated with contracting this disease, proper food safety measures should be applied to high-risk food products including poultry, beef, pork, lamb, eggs, and fresh produce.<ref name="Ehuwa O">Ehuwa O, Jaiswal AK, Jaiswal S. Salmonella, food safety and food handling practices. ''Foods''. 2021;10(5). doi:https://www.mdpi.com/2304-8158/10/5/907/htm </ref> Food manufacturers, ingredient suppliers, restaurants, and home cooks should practice sanitary processing procedures, store foods below 5&nbsp;°C, and thoroughly cook all foods to their designated safe-to-eat temperatures.<ref name="Ehuwa O" /> It has become increasingly difficult to mitigate the presence of salmonellosis infections across the human population due to the unique nature of multidrug-resistant serovars as a result of the counterproductive effects to use antibiotics as a broad spectrum treatment.<ref>{{Cite journal|title=Emergence of Multidrug-Resistant Salmonella enterica SerotypeTyphimurium DT104 Infections in the United States|first1=M. Kathleen|last1=Glynn|first2=Cheryl|last2=Bopp|first3=Wallis|last3=Dewitt|first4=Paul|last4=Dabney|first5=Mohammad|last5=Mokhtar|first6=Frederick J.|last6=Angulo|date=May 7, 1998|journal=New England Journal of Medicine|volume=338|issue=19|pages=1333–1339|doi=10.1056/NEJM199805073381901|doi-access=free|pmid=9571252 }}</ref> Key host [[immune deficiencies]] associated with [[HIV]], [[malaria]] and malnutrition have contributed to a wide spread of this disease and the need to use expensive [[antimicrobial drugs]] in the poorest health services in the world.<ref>{{cite journal |vauthors=Feasey NA, Dougan G, Kingsley RA, Heyderman RS, Gordon MA |date=June 2012 |title=Invasive non-typhoidal salmonella disease: an emerging and neglected tropical disease in Africa |journal=Lancet |volume=379 |issue=9835 |pages=2489–2499 |doi=10.1016/s0140-6736(11)61752-2 |pmc=3402672 |pmid=22587967}}</ref> But also bacterial factors, such as upregulated activity of the virulence gene ''pgtE'', due to a [[Single-nucleotide polymorphism|single nucleotide polymorphism]] (SNP) in its promoter region, have been shown to have a great impact upon the pathogenesis of this particular ''Salmonella'' sequence type.<ref>{{cite journal |display-authors=6 |vauthors=Hammarlöf DL, Kröger C, Owen SV, Canals R, Lacharme-Lora L, Wenner N, Schager AE, Wells TJ, Henderson IR, Wigley P, Hokamp K, Feasey NA, Gordon MA, Hinton JC |date=March 2018 |title=Role of a single noncoding nucleotide in the evolution of an epidemic African clade of ''Salmonella'' |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=115 |issue=11 |pages=E2614–E2623 |bibcode=2018PNAS..115E2614H |doi=10.1073/pnas.1714718115 |pmc=5856525 |pmid=29487214 |doi-access=free}}</ref>

== Survival and stress ==
There are factors that can increase the infection risk. These include a higher pH in the stomach, gastric resection, and treatment with anti acid buffering.<ref>{{cite journal|vauthors=Garcia del Portillo F, Foster JW, Finlay BB|year=1993|title=Role of acid tolerance response genes in ''Salmonella typhimurium'' virulence|journal=Infection and Immunity|volume=61|issue=10|pages=4489–4492|pmid=8406841|pmc=281185|doi=10.1128/iai.61.10.4489-4492.1993|doi-access=free}}</ref> If the stomach has a lower pH, then this helps as a [[innate immunity|defensive technique]] to potentially avoid infection.<ref>{{cite journal|vauthors=Foster JW, Hall HK|year=1990|title=Adaptive acidification tolerance response of ''Salmonella typhimurium''|journal=Journal of Bacteriology|volume=173|issue=2|pages=771–778|pmid=2404956|pmc=208505|doi=10.1128/jb.172.2.771-778.1990|doi-access=free}}</ref>

This strain is mesophilic and some can survive extremely low or high temperatures which can range from 2&nbsp;°C – 54&nbsp;°C.<ref>{{cite journal|vauthors=Kazmierczak MJ, Wiedmann M, Boor KJ|title=Alternative sigma factors and their roles in bacterial virulence|journal=Microbiology and Molecular Biology Reviews|volume=69|issue=4|pages=527–543|year=2005|pmid=16339734|pmc=1306804|doi=10.1128/MMBR.69.4.527-543.2005|doi-access=free}}</ref> [[Sigma factor]]s inside the cell control the gene expression and they can sense the changes in the environment from the outer membrane by activation of genes that then respond to heat stress and adapt accordingly.<ref>{{cite journal|vauthors=Spector MP, Kenyon WJ|title=Resistance and survival strategies of ''Salmonella enterica'' to environmental stresses|journal=Food Research International|volume=45|issue=2|pages=455–481|year=2012|doi=10.1016/j.foodres.2011.06.056|s2cid=84333218}}</ref> ''S. enterica'' also can quickly respond to cold temperatures by cold shock proteins (CSP) by synthesizing themselves so that the cell can later resume growth.<ref>{{cite journal|vauthors=Craig JE, Boyle D, Francis KP, Gallagher MP|title=Expression of the cold-shock gene cspB in ''Salmonella typhimurium'' occurs below a threshold temperature|journal=Microbiology|volume=144|issue=3|pages=697–704|year=1998|pmid=9534239|doi=10.1099/00221287-144-3-697|doi-access=free}}</ref> Chlorine can be a chemical stressor to ''S. enterica'' because once chlorine is present, ''S. enterica'' can produce a [[biofilm]] that provides itself with a exopolysaccharide matrix that has the ability of a chemical attack against chlorine.<ref>{{cite journal|vauthors=McDonnell G, Russell AD|title=Antiseptics and disinfectants: activity, action, and resistance|journal=Clinical Microbiology Reviews|volume=12|issue=1|pages=147–179|year=1999|pmid=9880479|pmc=88911|doi=10.1128/cmr.12.1.147|doi-access=free}}</ref> From this, chlorine has preventative measures for biofilm formation in poultry drinking systems and this reduces the risk of ''S. enterica''.<ref>{{cite journal|vauthors=Byrd JA, DeLoach JR, Corrier DE, Nisbet DJ, Stanker LH|title=Evaluation of ''Salmonella'' serotype distributions from commercial broiler hatcheries and grower houses|journal=Avian Diseases|volume=43|issue=1|pages=39–47|year=1999|pmid=10216758|doi=10.2307/1592760|jstor=1592760 }}</ref> Successful adaptation allows ''S. enterica'' to withstand more acidic conditions, counteracting stomach antibacterial effects.<ref>{{cite journal|vauthors=Rychlik I, Barrow PA|title=''Salmonella'' stress management and its relevance to behaviour during intestinal colonisation and infection|journal=FEMS Microbiology Reviews|volume=29|issue=5|pages=1021–1040|year=2005|doi=10.1016/j.femsre.2005.03.005|doi-access=free|pmid=16023758}}</ref>


== References ==
== References ==

Latest revision as of 01:39, 30 April 2024

Salmonella enterica subsp. enterica
Salmonella Typhimurium colonies on a Hektoen enteric agar plate
Scientific classification Edit this classification
Domain: Bacteria
Phylum: Pseudomonadota
Class: Gammaproteobacteria
Order: Enterobacterales
Family: Enterobacteriaceae
Genus: Salmonella
Species:
Subspecies:
S. e. subsp. enterica
Trinomial name
Salmonella enterica subsp. enterica

Salmonella enterica subsp. enterica is a subspecies of Salmonella enterica, the rod-shaped, flagellated, aerobic, Gram-negative bacterium. Many of the pathogenic serovars of the S. enterica species are in this subspecies, including that responsible for typhoid.[1]

Serovars[edit]

Salmonella enterica subsp. enterica serovars are defined based on their somatic (O) and flagellar (H) antigens, with over 2,600 serovars in total; only about 50 of these serovars are common causes of infections in humans.[2] Most of these serovars are found in the environment and survive in plants, water, and soil; many serovars have broad host ranges that allow them to colonize different species in mammals, birds, reptiles, amphibians, and insects. Zoonotic diseases, like Salmonella, spread between the environment and people.[3]

A number of techniques are currently used to differentiate between serotypes. These include looking for the presence or absence of antigens, phage typing, molecular fingerprinting and biotyping, where serovars are differentiated by which nutrients they are able to ferment. A possible factor in determining the host range of particular serovars is phage-mediated acquisition of a small number of genetic elements that enable infection of a particular host.[4] It is further postulated that serovars which infect a narrow range of species have diverged from ancestors with a broad host range, and have since specialised and lost the ability to infect some hosts.[5]

The CDC publishes a Salmonella Annual Report with a list of serovars most commonly associated with human illness, the top 10 serovars are listed below:[6]

Rank Serotype Percent
1 Enteritidis 16.8
2 Newport 10.1
3 Typhimurium 9.8
4 Javiana 5.8
5 I 4,[5],12:i:- 4.7
6 Infantis 2.7
7 Muenchen 2.6
8 Montevideo 2.2
9 Braenderup 2.1
10 Thompson 1.7
- Other 41.5

Studies have concluded most strains of Salmonella enterica subsp. enterica serovars possess serotype-specific virulence plasmids. These are plasmid-associated virulence characterized by low-copy-number plasmids and depending on the serovar, its size ranges from 50 to 100 kb.[7] In 2012, CDC's PulseNet became aware of a emergent multi-drug resistant Serovar Infantis SNP cluster, named REPJFX01. This SNP cluster has a large megaplasmid (pESI) that contains multiple drug-resistance genes.[8] The USDA NARMS stated that because of this pESI-plasmid, serovar Infantis is the leading serovar in poultry.[9] NCBI has over 12,500 isolates in the REPJFX01 SNP cluster, with over 3,700 being clinical isolates.[10] Serovar Enteritidis, which is the most common serovar isolated in human clinical cases, has also been found to produce endotoxins, coded by the stn and slyA genes, that attribute to the pathogenicity of Enteritidis.[11] Salmonella typhimurium notoriously known as the causative agent for typhoid can be used to deliver various cancer therapies. Tumors with their immune-suppressive microenvironments allow 1000 fold greater localization of engineered S. typhimurium than healthy tissues which are then able to enter tumor cells, lyse and deliver therapies.[12]

In November 2016, a new strain of extensively drug resistant (XDR) Salmonella enterica serovar Typhi emerged in Pakistan, primarily from the cities of Hyderabad and Karachi.[13] Multidrug resistant strains have been present since the late 1970s in Africa and Asia.[14] These XDR strains are resistant to all antibiotic treatment options: chloramphenicol, ampicillin, trimethoprim-sulfamethoxazole, fluoroquinolones, and third-generation cephalosporins. The outbreak has been ongoing since 2016.[15]

Nomenclature[edit]

The nomenclature of Salmonella enterica has long been a topic of debate in the microbiology community.[16] Originally in the 1880s, Salmonella species were named after the disease, host, or geological location they were associated with; however, this taxonomic characterization was contested due to genus members being categorized incompatibly with their genetic similarities. In the 1980s, the emergence of nucleotide sequencing and DNA hybridization led many established bacteriologists such as Le Minor and Popoff (1987), Euzéby (1999), and Ezaki and Yabuuchi (2000) to put forth their proposals for nomenclature changes.[17] It was not until 2005, that Le Minor and Popoff reproposed and established that "Salmonella enterica" would be the approved species name – excluding Salmonella bongori – and that Salmonella enterica contains six subspecies, of which Salmonella enterica subsp. enterica contains the most serovars.[18] Technological advancements allow researchers to use whole genome sequencing data to identify and group serovars using two methods: sequence typing and antigen recognition.[19]

Serovar names are capitalized but not italicized or underlined. Serovars may be designated in full form or short form (includes just the genus and serovar names). For example, in full designation Salmonella enterica subsp. enterica serovar Typhi is written as such, but in short designation it is written as Salmonella Typhi.[20] Each serovar can have many strains, as well, which allows for a rapid increase in the total number of antigenically variable bacteria.[21]

Epidemiology[edit]

The World Health Organization characterizes salmonellosis as a foodborne disease whose symptoms include diarrhea, fever, nausea, vomiting, and in severe cases death.[22] Salmonellosis has been assessed to primarily occur in human hosts due to bacterial colonization of the intestinal tract after the consumption of contaminated food or water, but it is also known to spread from person-to-person via the fecal-oral route.[23] To reduce the risk associated with contracting this disease, proper food safety measures should be applied to high-risk food products including poultry, beef, pork, lamb, eggs, and fresh produce.[24] Food manufacturers, ingredient suppliers, restaurants, and home cooks should practice sanitary processing procedures, store foods below 5 °C, and thoroughly cook all foods to their designated safe-to-eat temperatures.[24] It has become increasingly difficult to mitigate the presence of salmonellosis infections across the human population due to the unique nature of multidrug-resistant serovars as a result of the counterproductive effects to use antibiotics as a broad spectrum treatment.[25] Key host immune deficiencies associated with HIV, malaria and malnutrition have contributed to a wide spread of this disease and the need to use expensive antimicrobial drugs in the poorest health services in the world.[26] But also bacterial factors, such as upregulated activity of the virulence gene pgtE, due to a single nucleotide polymorphism (SNP) in its promoter region, have been shown to have a great impact upon the pathogenesis of this particular Salmonella sequence type.[27]

Survival and stress[edit]

There are factors that can increase the infection risk. These include a higher pH in the stomach, gastric resection, and treatment with anti acid buffering.[28] If the stomach has a lower pH, then this helps as a defensive technique to potentially avoid infection.[29]

This strain is mesophilic and some can survive extremely low or high temperatures which can range from 2 °C – 54 °C.[30] Sigma factors inside the cell control the gene expression and they can sense the changes in the environment from the outer membrane by activation of genes that then respond to heat stress and adapt accordingly.[31] S. enterica also can quickly respond to cold temperatures by cold shock proteins (CSP) by synthesizing themselves so that the cell can later resume growth.[32] Chlorine can be a chemical stressor to S. enterica because once chlorine is present, S. enterica can produce a biofilm that provides itself with a exopolysaccharide matrix that has the ability of a chemical attack against chlorine.[33] From this, chlorine has preventative measures for biofilm formation in poultry drinking systems and this reduces the risk of S. enterica.[34] Successful adaptation allows S. enterica to withstand more acidic conditions, counteracting stomach antibacterial effects.[35]

References[edit]

  1. ^ Murray PR, Rosenthal KS, Pfaller MA (2009). Medical Microbiology (6th ed.). Philadelphia, PA: Mosby Elsevier. p. 307.
  2. ^ Grimont PA, Weill FX (November 2007). "Antigenic formulae of the Salmonella serovars". WHO Collaborating Centre for Reference and Research on Salmonella. 9: 1–66.
  3. ^ Silva C, Calva E, Maloy S (February 2014). "One Health and Food-Borne Disease: Salmonella Transmission between Humans, Animals, and Plants". Microbiology Spectrum. 2 (1): OH-0020-2013. doi:10.1128/microbiolspec.OH-0020-2013. PMID 26082128.
  4. ^ Rabsch W, Andrews HL, Kingsley RA, Prager R, Tschäpe H, Adams LG, Bäumler AJ (May 2002). "Salmonella enterica serotype Typhimurium and its host-adapted variants". Infection and Immunity. 70 (5): 2249–2255. doi:10.1128/IAI.70.5.2249-2255.2002. PMC 127920. PMID 11953356.
  5. ^ Langridge GC, Fookes M, Connor TR, Feltwell T, Feasey N, Parsons BN, et al. (January 2015). "Patterns of genome evolution that have accompanied host adaptation in Salmonella". Proceedings of the National Academy of Sciences of the United States of America. 112 (3): 863–868. Bibcode:2015PNAS..112..863L. doi:10.1073/pnas.1416707112. PMC 4311825. PMID 25535353.
  6. ^ "National Enteric Disease Surveillance: Salmonella Annual Report, 2016" (PDF). CDC.gov. 2016.
  7. ^ Rotger R, Casadesús J (September 1999). "The virulence plasmids of Salmonella" (PDF). International Microbiology. 2 (3): 177–184. PMID 10943411.
  8. ^ CDC (2023-07-21). "Persistent Strain of Salmonella Infantis (REPJFX01) Linked to Chicken". Centers for Disease Control and Prevention. Retrieved 2023-11-19.
  9. ^ "FSIS NARMS Multi-Year Report – 2014-2019". fsis.usda.gov. 2023-02-10. Retrieved 2023-11-15.
  10. ^ "Isolates Browser - Pathogen Detection - NCBI". ncbi.nlm.nih.gov. Retrieved 2023-11-19.
  11. ^ Ashkenazi S, Cleary TG, Murray BE, Wanger A, Pickering LK (December 1988). "Quantitative analysis and partial characterization of cytotoxin production by Salmonella strains". Infection and Immunity. 56 (12): 3089–3094. doi:10.1128/iai.56.12.3089-3094.1988. PMC 259706. PMID 3182072.
  12. ^ Raman, Vishnu; Van Dessel, Nele; Hall, Christopher L.; Wetherby, Victoria E.; Whitney, Samantha A.; Kolewe, Emily L.; Bloom, Shoshana M. K.; Sharma, Abhinav; Hardy, Jeanne A.; Bollen, Mathieu; Van Eynde, Aleyde; Forbes, Neil S. (2021-10-21). "Intracellular delivery of protein drugs with an autonomously lysing bacterial system reduces tumor growth and metastases". Nature Communications. 12 (1): 6116. doi:10.1038/s41467-021-26367-9. ISSN 2041-1723. PMC 8531320. PMID 34675204.
  13. ^ Daley J (21 February 2018). "Typhoid Outbreak in Pakistan Linked to Extensively Drug-Resistant Bacteria". The Scientist Magazine®. Retrieved 2018-09-03.
  14. ^ Klemm EJ, Shakoor S, Page AJ, Qamar FN, Judge K, Saeed DK, et al. (February 2018). "Emergence of an Extensively Drug-Resistant Salmonella enterica Serovar Typhi Clone Harboring a Promiscuous Plasmid Encoding Resistance to Fluoroquinolones and Third-Generation Cephalosporins". mBio. 9 (1). doi:10.1128/mBio.00105-18. PMC 5821095. PMID 29463654.
  15. ^ "Extensively Drug-Resistant Typhoid Fever in Pakistan – Alert – Level 2, Practice Enhanced Precautions". Travel Health Notices. U.S. Centers for Disease Control and Prevention. Retrieved 2018-09-03.
  16. ^ Su LH, Chiu CH (2007). "Salmonella: clinical importance and evolution of nomenclature" (PDF). Chang Gung Medical Journal. 30 (3): 210–219. PMID 17760271.
  17. ^ Agbaje M, Begum RH, Oyekunle MA, Ojo OE, Adenubi OT (November 2011). "Evolution of Salmonella nomenclature: a critical note". Folia Microbiologica. 56 (6): 497–503. doi:10.1007/s12223-011-0075-4. PMID 22052214. S2CID 19799923.
  18. ^ Brenner FW, Villar RG, Angulo FJ, Tauxe R, Swaminathan B (July 2000). "Salmonella nomenclature". Journal of Clinical Microbiology. 38 (7): 2465–2467. doi:10.1128/JCM.38.7.2465-2467.2000. PMC 86943. PMID 10878026.
  19. ^ Chattaway MA, Langridge GC, Wain J (April 2021). "Salmonella nomenclature in the genomic era: a time for change". Scientific Reports. 11 (1): 7494. Bibcode:2021NatSR..11.7494C. doi:10.1038/s41598-021-86243-w. PMC 8021552. PMID 33820940.
  20. ^ "Scientific Nomenclature". Emerging Infectious Dieases. Centers for Disease Control and Prevention. Retrieved 17 February 2020.
  21. ^ "Salmonella spp. comparative sequencing". Wellcome Trust Genome Campus. Archived from the original on 2007-11-14.
  22. ^ "Salmonella (non-typhoidal)". www.who.int. Retrieved 2023-10-26.
  23. ^ Giannella, Ralph A. (1996), Baron, Samuel (ed.), "Salmonella", Medical Microbiology (4th ed.), Galveston (TX): University of Texas Medical Branch at Galveston, ISBN 978-0-9631172-1-2, PMID 21413334, retrieved 2023-10-26
  24. ^ a b Ehuwa O, Jaiswal AK, Jaiswal S. Salmonella, food safety and food handling practices. Foods. 2021;10(5). doi:https://www.mdpi.com/2304-8158/10/5/907/htm
  25. ^ Glynn, M. Kathleen; Bopp, Cheryl; Dewitt, Wallis; Dabney, Paul; Mokhtar, Mohammad; Angulo, Frederick J. (May 7, 1998). "Emergence of Multidrug-Resistant Salmonella enterica SerotypeTyphimurium DT104 Infections in the United States". New England Journal of Medicine. 338 (19): 1333–1339. doi:10.1056/NEJM199805073381901. PMID 9571252.
  26. ^ Feasey NA, Dougan G, Kingsley RA, Heyderman RS, Gordon MA (June 2012). "Invasive non-typhoidal salmonella disease: an emerging and neglected tropical disease in Africa". Lancet. 379 (9835): 2489–2499. doi:10.1016/s0140-6736(11)61752-2. PMC 3402672. PMID 22587967.
  27. ^ Hammarlöf DL, Kröger C, Owen SV, Canals R, Lacharme-Lora L, Wenner N, et al. (March 2018). "Role of a single noncoding nucleotide in the evolution of an epidemic African clade of Salmonella". Proceedings of the National Academy of Sciences of the United States of America. 115 (11): E2614–E2623. Bibcode:2018PNAS..115E2614H. doi:10.1073/pnas.1714718115. PMC 5856525. PMID 29487214.
  28. ^ Garcia del Portillo F, Foster JW, Finlay BB (1993). "Role of acid tolerance response genes in Salmonella typhimurium virulence". Infection and Immunity. 61 (10): 4489–4492. doi:10.1128/iai.61.10.4489-4492.1993. PMC 281185. PMID 8406841.
  29. ^ Foster JW, Hall HK (1990). "Adaptive acidification tolerance response of Salmonella typhimurium". Journal of Bacteriology. 173 (2): 771–778. doi:10.1128/jb.172.2.771-778.1990. PMC 208505. PMID 2404956.
  30. ^ Kazmierczak MJ, Wiedmann M, Boor KJ (2005). "Alternative sigma factors and their roles in bacterial virulence". Microbiology and Molecular Biology Reviews. 69 (4): 527–543. doi:10.1128/MMBR.69.4.527-543.2005. PMC 1306804. PMID 16339734.
  31. ^ Spector MP, Kenyon WJ (2012). "Resistance and survival strategies of Salmonella enterica to environmental stresses". Food Research International. 45 (2): 455–481. doi:10.1016/j.foodres.2011.06.056. S2CID 84333218.
  32. ^ Craig JE, Boyle D, Francis KP, Gallagher MP (1998). "Expression of the cold-shock gene cspB in Salmonella typhimurium occurs below a threshold temperature". Microbiology. 144 (3): 697–704. doi:10.1099/00221287-144-3-697. PMID 9534239.
  33. ^ McDonnell G, Russell AD (1999). "Antiseptics and disinfectants: activity, action, and resistance". Clinical Microbiology Reviews. 12 (1): 147–179. doi:10.1128/cmr.12.1.147. PMC 88911. PMID 9880479.
  34. ^ Byrd JA, DeLoach JR, Corrier DE, Nisbet DJ, Stanker LH (1999). "Evaluation of Salmonella serotype distributions from commercial broiler hatcheries and grower houses". Avian Diseases. 43 (1): 39–47. doi:10.2307/1592760. JSTOR 1592760. PMID 10216758.
  35. ^ Rychlik I, Barrow PA (2005). "Salmonella stress management and its relevance to behaviour during intestinal colonisation and infection". FEMS Microbiology Reviews. 29 (5): 1021–1040. doi:10.1016/j.femsre.2005.03.005. PMID 16023758.