The significance of cagA and vacA subtypes of Helicobacter pylori in the pathogenesis of inflammation and peptic ulceration

AIMS: To assess the significance of cagA and vacA subtypes of Helicobacter pylori in relation to inflammation and density of bacterial colonisation in vivo within a dyspeptic UK population. METHODS: Dyspeptic patients who were Helicobacter pylori positive had antral samples taken for histology and c...

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Veröffentlicht in:Journal of clinical pathology 1998-10, Vol.51 (10), p.761-764
Hauptverfasser: Gunn, M C, Stephens, J C, Stewart, J A, Rathbone, B J, West, K P
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container_issue 10
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container_title Journal of clinical pathology
container_volume 51
creator Gunn, M C
Stephens, J C
Stewart, J A
Rathbone, B J
West, K P
description AIMS: To assess the significance of cagA and vacA subtypes of Helicobacter pylori in relation to inflammation and density of bacterial colonisation in vivo within a dyspeptic UK population. METHODS: Dyspeptic patients who were Helicobacter pylori positive had antral samples taken for histology and culture. Gastroduodenal pathology was noted. The grade of bacterial density and inflammation was assessed using the Sydney system. Bacterial DNA was extracted and the vacA alleles and the cagA/gene typed using PCR. RESULTS: 120 patients were studied. There was high rate of cagA positive strains in this population. Bacterial density did not correlate with the presence of peptic ulceration. There was a significant association between cagA positive strains and increased inflammation and bacterial density. The vacA s1 type independently correlated with extensive chronic inflammation but there was no association with bacterial density. The vacA m type did not correlate with extent of inflammation or bacterial density. CONCLUSIONS: The results suggest that cagA is important in the pathogenesis of inflammation and peptic ulceration. These findings are in keeping with the hypothesis that cagA acts as a marker for a cag pathogenicity island which encodes several genes involved in inflammation. The vacA s1 allele correlates with inflammation independently of cagA, possibly through its enhanced ability to produce the vacuolating cytotoxin.
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METHODS: Dyspeptic patients who were Helicobacter pylori positive had antral samples taken for histology and culture. Gastroduodenal pathology was noted. The grade of bacterial density and inflammation was assessed using the Sydney system. Bacterial DNA was extracted and the vacA alleles and the cagA/gene typed using PCR. RESULTS: 120 patients were studied. There was high rate of cagA positive strains in this population. Bacterial density did not correlate with the presence of peptic ulceration. There was a significant association between cagA positive strains and increased inflammation and bacterial density. The vacA s1 type independently correlated with extensive chronic inflammation but there was no association with bacterial density. The vacA m type did not correlate with extent of inflammation or bacterial density. CONCLUSIONS: The results suggest that cagA is important in the pathogenesis of inflammation and peptic ulceration. These findings are in keeping with the hypothesis that cagA acts as a marker for a cag pathogenicity island which encodes several genes involved in inflammation. The vacA s1 allele correlates with inflammation independently of cagA, possibly through its enhanced ability to produce the vacuolating cytotoxin.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.51.10.761</identifier><identifier>PMID: 10023339</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antigens, Bacterial ; Bacterial diseases ; Bacterial diseases of the digestive system and abdomen ; Bacterial Proteins - genetics ; Bacterial Toxins - genetics ; Bacterial Typing Techniques ; Biological and medical sciences ; Female ; Gastritis - microbiology ; Helicobacter Infections - complications ; Helicobacter Infections - microbiology ; Helicobacter pylori - classification ; Helicobacter pylori - genetics ; Helicobacter pylori - pathogenicity ; Human bacterial diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Middle Aged ; Peptic Ulcer - microbiology ; Polymerase Chain Reaction ; Vacuoles</subject><ispartof>Journal of clinical pathology, 1998-10, Vol.51 (10), p.761-764</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b548t-6da0df3274fedd5d10c4ccb7e44b302c314a689e456db070a2b794733b8b49ed3</citedby><cites>FETCH-LOGICAL-b548t-6da0df3274fedd5d10c4ccb7e44b302c314a689e456db070a2b794733b8b49ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC500931/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC500931/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2411148$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10023339$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gunn, M C</creatorcontrib><creatorcontrib>Stephens, J C</creatorcontrib><creatorcontrib>Stewart, J A</creatorcontrib><creatorcontrib>Rathbone, B J</creatorcontrib><creatorcontrib>West, K P</creatorcontrib><title>The significance of cagA and vacA subtypes of Helicobacter pylori in the pathogenesis of inflammation and peptic ulceration</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>AIMS: To assess the significance of cagA and vacA subtypes of Helicobacter pylori in relation to inflammation and density of bacterial colonisation in vivo within a dyspeptic UK population. METHODS: Dyspeptic patients who were Helicobacter pylori positive had antral samples taken for histology and culture. Gastroduodenal pathology was noted. The grade of bacterial density and inflammation was assessed using the Sydney system. Bacterial DNA was extracted and the vacA alleles and the cagA/gene typed using PCR. RESULTS: 120 patients were studied. There was high rate of cagA positive strains in this population. Bacterial density did not correlate with the presence of peptic ulceration. There was a significant association between cagA positive strains and increased inflammation and bacterial density. The vacA s1 type independently correlated with extensive chronic inflammation but there was no association with bacterial density. The vacA m type did not correlate with extent of inflammation or bacterial density. CONCLUSIONS: The results suggest that cagA is important in the pathogenesis of inflammation and peptic ulceration. These findings are in keeping with the hypothesis that cagA acts as a marker for a cag pathogenicity island which encodes several genes involved in inflammation. The vacA s1 allele correlates with inflammation independently of cagA, possibly through its enhanced ability to produce the vacuolating cytotoxin.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens, Bacterial</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the digestive system and abdomen</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Toxins - genetics</subject><subject>Bacterial Typing Techniques</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Gastritis - microbiology</subject><subject>Helicobacter Infections - complications</subject><subject>Helicobacter Infections - microbiology</subject><subject>Helicobacter pylori - classification</subject><subject>Helicobacter pylori - genetics</subject><subject>Helicobacter pylori - pathogenicity</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Peptic Ulcer - microbiology</subject><subject>Polymerase Chain Reaction</subject><subject>Vacuoles</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2P0zAQxSMEYsvCkSvKAaG9pHhix24OHKqwsIgVXBaulu1MWpfEDna6ouKfx_1QWU6cRjPvN29Geln2EsgcgPK3GzPOK5inVnB4lM2AibJgwPjjbEZICUUtGL_InsW4IQSoAPo0u4CkUErrWfb7bo15tCtnO2uUM5j7LjdqtcyVa_N7ZZZ53OppN2LcKzfYW-O1MhOGfNz1PtjcunxKJqOa1n6FDqM9oNZ1vRoGNVnvDmYjjpM1-bY3GA7T59mTTvURX5zqZfbtw_Vdc1Pcfv34qVneFrpii6ngrSJtR0vBOmzbqgVimDFaIGOaktJQYIovamQVbzURRJVa1ExQqhea1djSy-zd0Xfc6gFbg24KqpdjsIMKO-mVlf8qzq7lyt_LipCaQtp_c9oP_ucW4yQHGw32vXLot1HyGgQRvEpgcQRN8DEG7M43gMh9WjKlJSvYtymtxL96-NgD-hhPAl6fABWN6ruQErLxzJUMANji710bJ_x1llX4IbmgopJfvjeSNZ-b91DXkif-6sjrYfOfF_8AELK79w</recordid><startdate>19981001</startdate><enddate>19981001</enddate><creator>Gunn, M C</creator><creator>Stephens, J C</creator><creator>Stewart, J A</creator><creator>Rathbone, B J</creator><creator>West, K P</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19981001</creationdate><title>The significance of cagA and vacA subtypes of Helicobacter pylori in the pathogenesis of inflammation and peptic ulceration</title><author>Gunn, M C ; Stephens, J C ; Stewart, J A ; Rathbone, B J ; West, K P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b548t-6da0df3274fedd5d10c4ccb7e44b302c314a689e456db070a2b794733b8b49ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens, Bacterial</topic><topic>Bacterial diseases</topic><topic>Bacterial diseases of the digestive system and abdomen</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Toxins - genetics</topic><topic>Bacterial Typing Techniques</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Gastritis - microbiology</topic><topic>Helicobacter Infections - complications</topic><topic>Helicobacter Infections - microbiology</topic><topic>Helicobacter pylori - classification</topic><topic>Helicobacter pylori - genetics</topic><topic>Helicobacter pylori - pathogenicity</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Peptic Ulcer - microbiology</topic><topic>Polymerase Chain Reaction</topic><topic>Vacuoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gunn, M C</creatorcontrib><creatorcontrib>Stephens, J C</creatorcontrib><creatorcontrib>Stewart, J A</creatorcontrib><creatorcontrib>Rathbone, B J</creatorcontrib><creatorcontrib>West, K P</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gunn, M C</au><au>Stephens, J C</au><au>Stewart, J A</au><au>Rathbone, B J</au><au>West, K P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The significance of cagA and vacA subtypes of Helicobacter pylori in the pathogenesis of inflammation and peptic ulceration</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>1998-10-01</date><risdate>1998</risdate><volume>51</volume><issue>10</issue><spage>761</spage><epage>764</epage><pages>761-764</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>AIMS: To assess the significance of cagA and vacA subtypes of Helicobacter pylori in relation to inflammation and density of bacterial colonisation in vivo within a dyspeptic UK population. METHODS: Dyspeptic patients who were Helicobacter pylori positive had antral samples taken for histology and culture. Gastroduodenal pathology was noted. The grade of bacterial density and inflammation was assessed using the Sydney system. Bacterial DNA was extracted and the vacA alleles and the cagA/gene typed using PCR. RESULTS: 120 patients were studied. There was high rate of cagA positive strains in this population. Bacterial density did not correlate with the presence of peptic ulceration. There was a significant association between cagA positive strains and increased inflammation and bacterial density. The vacA s1 type independently correlated with extensive chronic inflammation but there was no association with bacterial density. The vacA m type did not correlate with extent of inflammation or bacterial density. CONCLUSIONS: The results suggest that cagA is important in the pathogenesis of inflammation and peptic ulceration. These findings are in keeping with the hypothesis that cagA acts as a marker for a cag pathogenicity island which encodes several genes involved in inflammation. The vacA s1 allele correlates with inflammation independently of cagA, possibly through its enhanced ability to produce the vacuolating cytotoxin.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>10023339</pmid><doi>10.1136/jcp.51.10.761</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Antigens, Bacterial
Bacterial diseases
Bacterial diseases of the digestive system and abdomen
Bacterial Proteins - genetics
Bacterial Toxins - genetics
Bacterial Typing Techniques
Biological and medical sciences
Female
Gastritis - microbiology
Helicobacter Infections - complications
Helicobacter Infections - microbiology
Helicobacter pylori - classification
Helicobacter pylori - genetics
Helicobacter pylori - pathogenicity
Human bacterial diseases
Humans
Infectious diseases
Male
Medical sciences
Middle Aged
Peptic Ulcer - microbiology
Polymerase Chain Reaction
Vacuoles
title The significance of cagA and vacA subtypes of Helicobacter pylori in the pathogenesis of inflammation and peptic ulceration
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