Gram-negative bacteria killed by complement are associated with more severe biliary infections and produce more tumor necrosis factor-α in sera

Background. We previously showed that gallstones contain bacteria and that illness severity correlates with bacterial presence. This study examined virulence differences of gram-negative biliary bacteria. Methods. Gallstones and bile were cultured, and sera obtained, from 210 patients. Infection sev...

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Veröffentlicht in:Surgery 2002-08, Vol.132 (2), p.408-414
Hauptverfasser: Stewart, Lygia, Oesterle, Adair L., Griffiss, J.McLeod, Jarvis, Gary A., Aagaard, Beverly, Way, Lawrence W.
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container_end_page 414
container_issue 2
container_start_page 408
container_title Surgery
container_volume 132
creator Stewart, Lygia
Oesterle, Adair L.
Griffiss, J.McLeod
Jarvis, Gary A.
Aagaard, Beverly
Way, Lawrence W.
description Background. We previously showed that gallstones contain bacteria and that illness severity correlates with bacterial presence. This study examined virulence differences of gram-negative biliary bacteria. Methods. Gallstones and bile were cultured, and sera obtained, from 210 patients. Infection severity was staged as: none—no clinical infection; moderate—fever, leukocytosis; or severe—bacteremia, cholangitis, hypotension, abscess, or organ failure. Gram-negative biliary bacteria were tested against patient (and control) serum for complement-mediated bacterial killing and induction of tumor necrosis factor-α (TNFα) production (using cultured monocytes) with and without sera. These results were correlated with infection severity. Results. A total of 98 (47%) patients had biliary bacteria. Infection severity distribution was none, 29%; moderate, 35%; and severe, 36%. Gram-negative organisms killed by complement were associated with more severe infections as follows: 13%, none; 60%, moderate; and 88%, severe infections (P =.024 and P
doi_str_mv 10.1067/msy.2002.127423
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We previously showed that gallstones contain bacteria and that illness severity correlates with bacterial presence. This study examined virulence differences of gram-negative biliary bacteria. Methods. Gallstones and bile were cultured, and sera obtained, from 210 patients. Infection severity was staged as: none—no clinical infection; moderate—fever, leukocytosis; or severe—bacteremia, cholangitis, hypotension, abscess, or organ failure. Gram-negative biliary bacteria were tested against patient (and control) serum for complement-mediated bacterial killing and induction of tumor necrosis factor-α (TNFα) production (using cultured monocytes) with and without sera. These results were correlated with infection severity. Results. A total of 98 (47%) patients had biliary bacteria. Infection severity distribution was none, 29%; moderate, 35%; and severe, 36%. Gram-negative organisms killed by complement were associated with more severe infections as follows: 13%, none; 60%, moderate; and 88%, severe infections (P =.024 and P &lt;.0001, respectively vs none, chi-square test). TNFα production in sera increased 182 pg/mL with complement resistant bacteria, but increased 546 pg/mL with bacteria killed by complement (P &lt;.0001, killed vs not killed, Student's t test). E coli and Klebsiella were the most virulent bacterial species. They were cultured from blood, usually killed by complement, and had the largest increase in TNFα production in sera. Conclusions. Gram-negative biliary bacteria killed by complement (as opposed to complement-resistant) were associated with more serious biliary infections including bacteremia and induced more TNFα production in sera. This suggests a potential role for complement activation and cytokine production in biliary sepsis. (Surgery 2002;132:408-14.)</description><identifier>ISSN: 0039-6060</identifier><identifier>EISSN: 1532-7361</identifier><identifier>DOI: 10.1067/msy.2002.127423</identifier><identifier>PMID: 12219042</identifier><identifier>CODEN: SURGAZ</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Biliary Tract - immunology ; Biliary Tract - microbiology ; Biological and medical sciences ; Cholelithiasis - immunology ; Cholelithiasis - microbiology ; Complement Activation - immunology ; Complement System Proteins - immunology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Gram-Negative Bacteria - immunology ; Gram-Negative Bacterial Infections - immunology ; Humans ; In Vitro Techniques ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Tumor Necrosis Factor-alpha - biosynthesis ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>Surgery, 2002-08, Vol.132 (2), p.408-414</ispartof><rights>2002</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-1dd22f39cda14dd48731ce3746d5013c25e9544011c7c963340262585268a40b3</citedby><cites>FETCH-LOGICAL-c373t-1dd22f39cda14dd48731ce3746d5013c25e9544011c7c963340262585268a40b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0039606002001034$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,23909,23910,25118,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13923157$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12219042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stewart, Lygia</creatorcontrib><creatorcontrib>Oesterle, Adair L.</creatorcontrib><creatorcontrib>Griffiss, J.McLeod</creatorcontrib><creatorcontrib>Jarvis, Gary A.</creatorcontrib><creatorcontrib>Aagaard, Beverly</creatorcontrib><creatorcontrib>Way, Lawrence W.</creatorcontrib><title>Gram-negative bacteria killed by complement are associated with more severe biliary infections and produce more tumor necrosis factor-α in sera</title><title>Surgery</title><addtitle>Surgery</addtitle><description>Background. We previously showed that gallstones contain bacteria and that illness severity correlates with bacterial presence. This study examined virulence differences of gram-negative biliary bacteria. Methods. Gallstones and bile were cultured, and sera obtained, from 210 patients. Infection severity was staged as: none—no clinical infection; moderate—fever, leukocytosis; or severe—bacteremia, cholangitis, hypotension, abscess, or organ failure. Gram-negative biliary bacteria were tested against patient (and control) serum for complement-mediated bacterial killing and induction of tumor necrosis factor-α (TNFα) production (using cultured monocytes) with and without sera. These results were correlated with infection severity. Results. A total of 98 (47%) patients had biliary bacteria. Infection severity distribution was none, 29%; moderate, 35%; and severe, 36%. Gram-negative organisms killed by complement were associated with more severe infections as follows: 13%, none; 60%, moderate; and 88%, severe infections (P =.024 and P &lt;.0001, respectively vs none, chi-square test). TNFα production in sera increased 182 pg/mL with complement resistant bacteria, but increased 546 pg/mL with bacteria killed by complement (P &lt;.0001, killed vs not killed, Student's t test). E coli and Klebsiella were the most virulent bacterial species. They were cultured from blood, usually killed by complement, and had the largest increase in TNFα production in sera. Conclusions. Gram-negative biliary bacteria killed by complement (as opposed to complement-resistant) were associated with more serious biliary infections including bacteremia and induced more TNFα production in sera. This suggests a potential role for complement activation and cytokine production in biliary sepsis. (Surgery 2002;132:408-14.)</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biliary Tract - immunology</subject><subject>Biliary Tract - microbiology</subject><subject>Biological and medical sciences</subject><subject>Cholelithiasis - immunology</subject><subject>Cholelithiasis - microbiology</subject><subject>Complement Activation - immunology</subject><subject>Complement System Proteins - immunology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gram-Negative Bacteria - immunology</subject><subject>Gram-Negative Bacterial Infections - immunology</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0039-6060</issn><issn>1532-7361</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9u1DAQxi1ERZfCmRvyBW7Zjv8k3hxRBQWpEpdythx7AobEXmxn0b5FX6UvwjPhVVbqidNI9m---WY-Qt4w2DLo1PWcj1sOwLeMK8nFM7JhreCNEh17TjYAom866OCSvMz5JwD0ku1ekEvGOetB8g15uE1mbgJ-N8UfkA7GFkze0F9-mtDR4UhtnPcTzhgKNQmpyTlab0r9_OPLDzrH-pjxgLUMfvImHakPI9riY8jUBEf3KbrF4oqWpRYa0KaYfaZjHRhT8_exNlWZZF6Ri9FMGV-f6xX59unj_c3n5u7r7ZebD3eNFUqUhjnH-Sh66wyTzsmdEsyiULJzLTBheYt9KyUwZpXtOyEk8I63u5Z3OyNhEFfk_apb3f1eMBc9-2xxmkzAuGStOCjVSlXB6xU8Oc4JR71Pfq5ragb6FIKuIehTCHoNoXa8PUsvw4zuiT9fvQLvzoDJ1kxjMsH6_MSJngvWnkb3K4f1EAePSWfrMVh0PtUDaxf9f038A8QZpRM</recordid><startdate>20020801</startdate><enddate>20020801</enddate><creator>Stewart, Lygia</creator><creator>Oesterle, Adair L.</creator><creator>Griffiss, J.McLeod</creator><creator>Jarvis, Gary A.</creator><creator>Aagaard, Beverly</creator><creator>Way, Lawrence W.</creator><general>Mosby, Inc</general><general>Elsevier</general><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></search><sort><creationdate>20020801</creationdate><title>Gram-negative bacteria killed by complement are associated with more severe biliary infections and produce more tumor necrosis factor-α in sera</title><author>Stewart, Lygia ; Oesterle, Adair L. ; Griffiss, J.McLeod ; Jarvis, Gary A. ; Aagaard, Beverly ; Way, Lawrence W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-1dd22f39cda14dd48731ce3746d5013c25e9544011c7c963340262585268a40b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biliary Tract - immunology</topic><topic>Biliary Tract - microbiology</topic><topic>Biological and medical sciences</topic><topic>Cholelithiasis - immunology</topic><topic>Cholelithiasis - microbiology</topic><topic>Complement Activation - immunology</topic><topic>Complement System Proteins - immunology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gram-Negative Bacteria - immunology</topic><topic>Gram-Negative Bacterial Infections - immunology</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stewart, Lygia</creatorcontrib><creatorcontrib>Oesterle, Adair L.</creatorcontrib><creatorcontrib>Griffiss, J.McLeod</creatorcontrib><creatorcontrib>Jarvis, Gary A.</creatorcontrib><creatorcontrib>Aagaard, Beverly</creatorcontrib><creatorcontrib>Way, Lawrence W.</creatorcontrib><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><jtitle>Surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stewart, Lygia</au><au>Oesterle, Adair L.</au><au>Griffiss, J.McLeod</au><au>Jarvis, Gary A.</au><au>Aagaard, Beverly</au><au>Way, Lawrence W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gram-negative bacteria killed by complement are associated with more severe biliary infections and produce more tumor necrosis factor-α in sera</atitle><jtitle>Surgery</jtitle><addtitle>Surgery</addtitle><date>2002-08-01</date><risdate>2002</risdate><volume>132</volume><issue>2</issue><spage>408</spage><epage>414</epage><pages>408-414</pages><issn>0039-6060</issn><eissn>1532-7361</eissn><coden>SURGAZ</coden><abstract>Background. We previously showed that gallstones contain bacteria and that illness severity correlates with bacterial presence. This study examined virulence differences of gram-negative biliary bacteria. Methods. Gallstones and bile were cultured, and sera obtained, from 210 patients. Infection severity was staged as: none—no clinical infection; moderate—fever, leukocytosis; or severe—bacteremia, cholangitis, hypotension, abscess, or organ failure. Gram-negative biliary bacteria were tested against patient (and control) serum for complement-mediated bacterial killing and induction of tumor necrosis factor-α (TNFα) production (using cultured monocytes) with and without sera. These results were correlated with infection severity. Results. A total of 98 (47%) patients had biliary bacteria. Infection severity distribution was none, 29%; moderate, 35%; and severe, 36%. Gram-negative organisms killed by complement were associated with more severe infections as follows: 13%, none; 60%, moderate; and 88%, severe infections (P =.024 and P &lt;.0001, respectively vs none, chi-square test). TNFα production in sera increased 182 pg/mL with complement resistant bacteria, but increased 546 pg/mL with bacteria killed by complement (P &lt;.0001, killed vs not killed, Student's t test). E coli and Klebsiella were the most virulent bacterial species. They were cultured from blood, usually killed by complement, and had the largest increase in TNFα production in sera. Conclusions. Gram-negative biliary bacteria killed by complement (as opposed to complement-resistant) were associated with more serious biliary infections including bacteremia and induced more TNFα production in sera. This suggests a potential role for complement activation and cytokine production in biliary sepsis. (Surgery 2002;132:408-14.)</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>12219042</pmid><doi>10.1067/msy.2002.127423</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Biliary Tract - immunology
Biliary Tract - microbiology
Biological and medical sciences
Cholelithiasis - immunology
Cholelithiasis - microbiology
Complement Activation - immunology
Complement System Proteins - immunology
Female
Gastroenterology. Liver. Pancreas. Abdomen
Gram-Negative Bacteria - immunology
Gram-Negative Bacterial Infections - immunology
Humans
In Vitro Techniques
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Middle Aged
Other diseases. Semiology
Tumor Necrosis Factor-alpha - biosynthesis
Tumor Necrosis Factor-alpha - metabolism
title Gram-negative bacteria killed by complement are associated with more severe biliary infections and produce more tumor necrosis factor-α in sera
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