Specimens and culture media for the laboratory diagnosis of typhoid fever
Culture of S. Typhi is necessary for the definitive diagnosis of typhoid fever and provides isolates for antibiotic susceptibility testing and epidemiological studies. However, current methods are not fully optimised and sourcing culture media and bottles for culture media may be problematic. In two...
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Veröffentlicht in: | Journal of infection in developing countries 2008-12, Vol.2 (6), p.469-474 |
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container_title | Journal of infection in developing countries |
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creator | Wain, John Diep, To Song Bay, Phan Van Be Walsh, Amanda L Vinh, Ha Duong, Nguyen M Ho, Vo Anh Hien, Tran T Farrar, Jeremy White, Nicholas J Parry, Christopher M Day, Nicholas P J |
description | Culture of S. Typhi is necessary for the definitive diagnosis of typhoid fever and provides isolates for antibiotic susceptibility testing and epidemiological studies. However, current methods are not fully optimised and sourcing culture media and bottles for culture media may be problematic.
In two hospital laboratories in Viet Nam, comparisons of media for blood and stool culture were conducted. The effect of the volume of blood or stool on culture positivity rate was examined and direct plating of the blood buffy coat was trialed.
For 148 suspected typhoid fever cases, ox bile broth (58 positive) and brain-heart infusion broth containing saponin (63 positive), performed equally well. For 69 confirmed adult typhoid fever cases, large-volume (15 ml) blood culture gave the same sensitivity as 1 ml of bone marrow culture. For 44 confirmed typhoid fever cases, the direct plating of the buffy coat was positive in 28 cases. For 263 positive stool cultures, selenite F and selenite mannitol performed equally well and culturing 2 g rather than 1g increased the isolation rate by 10.5%.
For the diagnosis of typhoid fever by blood culture the medium should be a rich nutrient broth containing a lysing agent. In adults 1 ml bone marrow or 15 ml blood culture gave similar results. Where isolates are needed for susceptibility testing or epidemiological studies, but resources for culture are scarce, direct plating of the blood buffy coat can be used with a 50% fall in sensitivity compared to standard blood culture. |
doi_str_mv | 10.3855/jidc.164 |
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In two hospital laboratories in Viet Nam, comparisons of media for blood and stool culture were conducted. The effect of the volume of blood or stool on culture positivity rate was examined and direct plating of the blood buffy coat was trialed.
For 148 suspected typhoid fever cases, ox bile broth (58 positive) and brain-heart infusion broth containing saponin (63 positive), performed equally well. For 69 confirmed adult typhoid fever cases, large-volume (15 ml) blood culture gave the same sensitivity as 1 ml of bone marrow culture. For 44 confirmed typhoid fever cases, the direct plating of the buffy coat was positive in 28 cases. For 263 positive stool cultures, selenite F and selenite mannitol performed equally well and culturing 2 g rather than 1g increased the isolation rate by 10.5%.
For the diagnosis of typhoid fever by blood culture the medium should be a rich nutrient broth containing a lysing agent. In adults 1 ml bone marrow or 15 ml blood culture gave similar results. Where isolates are needed for susceptibility testing or epidemiological studies, but resources for culture are scarce, direct plating of the blood buffy coat can be used with a 50% fall in sensitivity compared to standard blood culture.</description><identifier>ISSN: 2036-6590</identifier><identifier>EISSN: 1972-2680</identifier><identifier>DOI: 10.3855/jidc.164</identifier><identifier>PMID: 19745526</identifier><language>eng</language><publisher>Italy: Journal of Infection in Developing Countries</publisher><subject>Adult ; Bone marrow ; Bone Marrow - microbiology ; Child ; Clinical Laboratory Techniques ; Culture Media - chemistry ; Culture Techniques - methods ; Feces - microbiology ; Humans ; Laboratories ; Laboratories, Hospital ; Mannitol - chemistry ; Salmonella typhi - isolation & purification ; Sensitivity and Specificity ; Sodium Selenite - chemistry ; Typhoid ; Typhoid Fever - blood ; Typhoid Fever - diagnosis ; Vietnam</subject><ispartof>Journal of infection in developing countries, 2008-12, Vol.2 (6), p.469-474</ispartof><rights>2008. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c310t-8bf55e0aaf31fd3b648ad5b0e902d86723dd9f54c4996119cb059e7bef642eb93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19745526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wain, John</creatorcontrib><creatorcontrib>Diep, To Song</creatorcontrib><creatorcontrib>Bay, Phan Van Be</creatorcontrib><creatorcontrib>Walsh, Amanda L</creatorcontrib><creatorcontrib>Vinh, Ha</creatorcontrib><creatorcontrib>Duong, Nguyen M</creatorcontrib><creatorcontrib>Ho, Vo Anh</creatorcontrib><creatorcontrib>Hien, Tran T</creatorcontrib><creatorcontrib>Farrar, Jeremy</creatorcontrib><creatorcontrib>White, Nicholas J</creatorcontrib><creatorcontrib>Parry, Christopher M</creatorcontrib><creatorcontrib>Day, Nicholas P J</creatorcontrib><title>Specimens and culture media for the laboratory diagnosis of typhoid fever</title><title>Journal of infection in developing countries</title><addtitle>J Infect Dev Ctries</addtitle><description>Culture of S. Typhi is necessary for the definitive diagnosis of typhoid fever and provides isolates for antibiotic susceptibility testing and epidemiological studies. However, current methods are not fully optimised and sourcing culture media and bottles for culture media may be problematic.
In two hospital laboratories in Viet Nam, comparisons of media for blood and stool culture were conducted. The effect of the volume of blood or stool on culture positivity rate was examined and direct plating of the blood buffy coat was trialed.
For 148 suspected typhoid fever cases, ox bile broth (58 positive) and brain-heart infusion broth containing saponin (63 positive), performed equally well. For 69 confirmed adult typhoid fever cases, large-volume (15 ml) blood culture gave the same sensitivity as 1 ml of bone marrow culture. For 44 confirmed typhoid fever cases, the direct plating of the buffy coat was positive in 28 cases. For 263 positive stool cultures, selenite F and selenite mannitol performed equally well and culturing 2 g rather than 1g increased the isolation rate by 10.5%.
For the diagnosis of typhoid fever by blood culture the medium should be a rich nutrient broth containing a lysing agent. In adults 1 ml bone marrow or 15 ml blood culture gave similar results. Where isolates are needed for susceptibility testing or epidemiological studies, but resources for culture are scarce, direct plating of the blood buffy coat can be used with a 50% fall in sensitivity compared to standard blood culture.</description><subject>Adult</subject><subject>Bone marrow</subject><subject>Bone Marrow - microbiology</subject><subject>Child</subject><subject>Clinical Laboratory Techniques</subject><subject>Culture Media - chemistry</subject><subject>Culture Techniques - methods</subject><subject>Feces - microbiology</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Laboratories, Hospital</subject><subject>Mannitol - chemistry</subject><subject>Salmonella typhi - isolation & purification</subject><subject>Sensitivity and Specificity</subject><subject>Sodium Selenite - chemistry</subject><subject>Typhoid</subject><subject>Typhoid Fever - blood</subject><subject>Typhoid Fever - diagnosis</subject><subject>Vietnam</subject><issn>2036-6590</issn><issn>1972-2680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpd0F1LwzAUgOEgiptT8BdIwAu96cxHkzaXMvwYDLxQr0PanLiOtplJK-zfm7GB4NWBw8Ph8CJ0Tcmcl0I8bBpbz6nMT9CUqoJlTJbkFE0Z4TKTQpEJuohxQ4hQXNBzNEkoF4LJKVq-b6FuOugjNr3F9dgOYwDcgW0Mdj7gYQ24NZUPZvBhh9P6q_exidg7POy2a99Y7OAHwiU6c6aNcHWcM_T5_PSxeM1Wby_LxeMqqzklQ1ZWTgggxjhOneWVzEtjRUVAEWZLWTBurXIir3OlJKWqrtLXUFTgZM6gUnyG7g53t8F_jxAH3TWxhrY1Pfgx6oLnJGeMsCRv_8mNH0OfntNMSMJJoQRN6v6g6uBjDOD0NjSdCTtNid7X1fu6OtVN9OZ4cKxSoT94zMl_AethdOg</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Wain, John</creator><creator>Diep, To Song</creator><creator>Bay, Phan Van Be</creator><creator>Walsh, Amanda L</creator><creator>Vinh, Ha</creator><creator>Duong, Nguyen M</creator><creator>Ho, Vo Anh</creator><creator>Hien, Tran T</creator><creator>Farrar, Jeremy</creator><creator>White, Nicholas J</creator><creator>Parry, Christopher M</creator><creator>Day, Nicholas P J</creator><general>Journal of Infection in Developing Countries</general><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>8C1</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>Specimens and culture media for the laboratory diagnosis of typhoid fever</title><author>Wain, John ; Diep, To Song ; Bay, Phan Van Be ; Walsh, Amanda L ; Vinh, Ha ; Duong, Nguyen M ; Ho, Vo Anh ; Hien, Tran T ; Farrar, Jeremy ; White, Nicholas J ; Parry, Christopher M ; Day, Nicholas P J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-8bf55e0aaf31fd3b648ad5b0e902d86723dd9f54c4996119cb059e7bef642eb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Bone marrow</topic><topic>Bone Marrow - microbiology</topic><topic>Child</topic><topic>Clinical Laboratory Techniques</topic><topic>Culture Media - chemistry</topic><topic>Culture Techniques - methods</topic><topic>Feces - microbiology</topic><topic>Humans</topic><topic>Laboratories</topic><topic>Laboratories, Hospital</topic><topic>Mannitol - chemistry</topic><topic>Salmonella typhi - isolation & purification</topic><topic>Sensitivity and Specificity</topic><topic>Sodium Selenite - chemistry</topic><topic>Typhoid</topic><topic>Typhoid Fever - blood</topic><topic>Typhoid Fever - diagnosis</topic><topic>Vietnam</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wain, John</creatorcontrib><creatorcontrib>Diep, To Song</creatorcontrib><creatorcontrib>Bay, Phan Van Be</creatorcontrib><creatorcontrib>Walsh, Amanda L</creatorcontrib><creatorcontrib>Vinh, Ha</creatorcontrib><creatorcontrib>Duong, Nguyen M</creatorcontrib><creatorcontrib>Ho, Vo Anh</creatorcontrib><creatorcontrib>Hien, Tran T</creatorcontrib><creatorcontrib>Farrar, Jeremy</creatorcontrib><creatorcontrib>White, Nicholas J</creatorcontrib><creatorcontrib>Parry, Christopher M</creatorcontrib><creatorcontrib>Day, Nicholas P J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Public Health Database</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of infection in developing countries</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wain, John</au><au>Diep, To Song</au><au>Bay, Phan Van Be</au><au>Walsh, Amanda L</au><au>Vinh, Ha</au><au>Duong, Nguyen M</au><au>Ho, Vo Anh</au><au>Hien, Tran T</au><au>Farrar, Jeremy</au><au>White, Nicholas J</au><au>Parry, Christopher M</au><au>Day, Nicholas P J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Specimens and culture media for the laboratory diagnosis of typhoid fever</atitle><jtitle>Journal of infection in developing countries</jtitle><addtitle>J Infect Dev Ctries</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>2</volume><issue>6</issue><spage>469</spage><epage>474</epage><pages>469-474</pages><issn>2036-6590</issn><eissn>1972-2680</eissn><abstract>Culture of S. Typhi is necessary for the definitive diagnosis of typhoid fever and provides isolates for antibiotic susceptibility testing and epidemiological studies. However, current methods are not fully optimised and sourcing culture media and bottles for culture media may be problematic.
In two hospital laboratories in Viet Nam, comparisons of media for blood and stool culture were conducted. The effect of the volume of blood or stool on culture positivity rate was examined and direct plating of the blood buffy coat was trialed.
For 148 suspected typhoid fever cases, ox bile broth (58 positive) and brain-heart infusion broth containing saponin (63 positive), performed equally well. For 69 confirmed adult typhoid fever cases, large-volume (15 ml) blood culture gave the same sensitivity as 1 ml of bone marrow culture. For 44 confirmed typhoid fever cases, the direct plating of the buffy coat was positive in 28 cases. For 263 positive stool cultures, selenite F and selenite mannitol performed equally well and culturing 2 g rather than 1g increased the isolation rate by 10.5%.
For the diagnosis of typhoid fever by blood culture the medium should be a rich nutrient broth containing a lysing agent. In adults 1 ml bone marrow or 15 ml blood culture gave similar results. Where isolates are needed for susceptibility testing or epidemiological studies, but resources for culture are scarce, direct plating of the blood buffy coat can be used with a 50% fall in sensitivity compared to standard blood culture.</abstract><cop>Italy</cop><pub>Journal of Infection in Developing Countries</pub><pmid>19745526</pmid><doi>10.3855/jidc.164</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Bone marrow Bone Marrow - microbiology Child Clinical Laboratory Techniques Culture Media - chemistry Culture Techniques - methods Feces - microbiology Humans Laboratories Laboratories, Hospital Mannitol - chemistry Salmonella typhi - isolation & purification Sensitivity and Specificity Sodium Selenite - chemistry Typhoid Typhoid Fever - blood Typhoid Fever - diagnosis Vietnam |
title | Specimens and culture media for the laboratory diagnosis of typhoid fever |
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