Establishment of a Fast Diagnostic Method for Sepsis Pathogens Based on M1 Bead Enrichment
Blood culture-based sepsis diagnostic methods usually cannot obtain positive results in a timely manner. Molecular diagnostic methods, such as real-time PCR without blood culture, would be more time-saving and suitable for pathogenic diagnosis of sepsis, while their sensitivities have always been un...
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Veröffentlicht in: | Current microbiology 2023-05, Vol.80 (5), p.166-166, Article 166 |
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creator | Zheng, Hao Chen, Xiaoli Li, Wenge Lu, Jinxing Chen, Xiaoping |
description | Blood culture-based sepsis diagnostic methods usually cannot obtain positive results in a timely manner. Molecular diagnostic methods, such as real-time PCR without blood culture, would be more time-saving and suitable for pathogenic diagnosis of sepsis, while their sensitivities have always been unsatisfactory for the usually low concentration of pathogens in the blood of sepsis patients. In this study, we established a fast diagnostic method using magnetic beads coated with human recombined mannose-binding lectin that makes it possible to concentrate pathogens from human plasma that have low concentrations of pathogens. With subsequent microculture (MC) and real-time PCR, this method allowed the detection of 1–10 CFUs/ml of
Staphylococcus aureus
, Group A
Streptococcus
,
Escherichia coli
,
Pseudomonas aeruginosa
,
Candida tropicalis,
or
C. albicans
from human plasma within 9.5 h, which was 21–80 h earlier than blood culture. The combination of pathogen enrichment and MC made the detection of sepsis-causing pathogens more time-saving and more sensitive than blood culture or real-time PCR alone. |
doi_str_mv | 10.1007/s00284-023-03280-6 |
format | Article |
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Staphylococcus aureus
, Group A
Streptococcus
,
Escherichia coli
,
Pseudomonas aeruginosa
,
Candida tropicalis,
or
C. albicans
from human plasma within 9.5 h, which was 21–80 h earlier than blood culture. The combination of pathogen enrichment and MC made the detection of sepsis-causing pathogens more time-saving and more sensitive than blood culture or real-time PCR alone.</description><identifier>ISSN: 0343-8651</identifier><identifier>EISSN: 1432-0991</identifier><identifier>DOI: 10.1007/s00284-023-03280-6</identifier><identifier>PMID: 37022487</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Bacteria ; Beads ; Biomedical and Life Sciences ; Biotechnology ; Blood ; Blood culture ; Blood plasma ; Candida albicans ; Candida tropicalis ; Culture ; Diagnostic systems ; E coli ; Escherichia coli ; Escherichia coli - genetics ; Humans ; lectins ; Life Sciences ; Low concentrations ; magnetism ; Mannose ; Mannose-binding lectin ; Microbiology ; Pathogens ; Pseudomonas aeruginosa ; quantitative polymerase chain reaction ; Real time ; Real-Time Polymerase Chain Reaction - methods ; Sepsis ; Sepsis - diagnosis ; Staphylococcal Infections ; Staphylococcus aureus ; Staphylococcus aureus - genetics ; Streptococcus</subject><ispartof>Current microbiology, 2023-05, Vol.80 (5), p.166-166, Article 166</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-c983274dcd8d5566d8ee2f14e412f19ef8918ebfd21c00965087d035d827d5ab3</citedby><cites>FETCH-LOGICAL-c408t-c983274dcd8d5566d8ee2f14e412f19ef8918ebfd21c00965087d035d827d5ab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00284-023-03280-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00284-023-03280-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37022487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Hao</creatorcontrib><creatorcontrib>Chen, Xiaoli</creatorcontrib><creatorcontrib>Li, Wenge</creatorcontrib><creatorcontrib>Lu, Jinxing</creatorcontrib><creatorcontrib>Chen, Xiaoping</creatorcontrib><title>Establishment of a Fast Diagnostic Method for Sepsis Pathogens Based on M1 Bead Enrichment</title><title>Current microbiology</title><addtitle>Curr Microbiol</addtitle><addtitle>Curr Microbiol</addtitle><description>Blood culture-based sepsis diagnostic methods usually cannot obtain positive results in a timely manner. Molecular diagnostic methods, such as real-time PCR without blood culture, would be more time-saving and suitable for pathogenic diagnosis of sepsis, while their sensitivities have always been unsatisfactory for the usually low concentration of pathogens in the blood of sepsis patients. In this study, we established a fast diagnostic method using magnetic beads coated with human recombined mannose-binding lectin that makes it possible to concentrate pathogens from human plasma that have low concentrations of pathogens. With subsequent microculture (MC) and real-time PCR, this method allowed the detection of 1–10 CFUs/ml of
Staphylococcus aureus
, Group A
Streptococcus
,
Escherichia coli
,
Pseudomonas aeruginosa
,
Candida tropicalis,
or
C. albicans
from human plasma within 9.5 h, which was 21–80 h earlier than blood culture. The combination of pathogen enrichment and MC made the detection of sepsis-causing pathogens more time-saving and more sensitive than blood culture or real-time PCR alone.</description><subject>Bacteria</subject><subject>Beads</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Blood</subject><subject>Blood culture</subject><subject>Blood plasma</subject><subject>Candida albicans</subject><subject>Candida tropicalis</subject><subject>Culture</subject><subject>Diagnostic systems</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Humans</subject><subject>lectins</subject><subject>Life Sciences</subject><subject>Low concentrations</subject><subject>magnetism</subject><subject>Mannose</subject><subject>Mannose-binding lectin</subject><subject>Microbiology</subject><subject>Pathogens</subject><subject>Pseudomonas aeruginosa</subject><subject>quantitative polymerase chain reaction</subject><subject>Real time</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Sepsis</subject><subject>Sepsis - diagnosis</subject><subject>Staphylococcal Infections</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - genetics</subject><subject>Streptococcus</subject><issn>0343-8651</issn><issn>1432-0991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkU1PGzEQhi3UClLgD3BAlnrhsu34Y732sUBoK4GKBFy4WM56NixK1qlnc-Df1yF8SD20p5FmnnnH1sPYkYAvAqD5SgDS6gqkqkBJC5XZYROhlazAOfGBTUBpVVlTiz32iegRQEgHYpftqQak1LaZsPspjWG26OlhicPIU8cDvwg08vM-zIdEY9_yKxwfUuRdyvwGV9QTvw6lM8eB-GkgjDwN_ErwUwyRT4fct89hB-xjFxaEhy91n91dTG_PflSXv77_PPt2WbUa7Fi1zirZ6NhGG-vamGgRZSc0alGKw846YXHWRSlaAGdqsE0EVUcrm1iHmdpnJ9vcVU6_10ijX_bU4mIRBkxr8go0KFNOiP-isnGN0OVBG_TzX-hjWuehfGRDGWOcBiiU3FJtTkQZO7_K_TLkJy_AbyT5rSRfJPlnSd6UpeOX6PVsifFt5dVKAdQWoDIa5pjfb_8j9g-3fZn2</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Zheng, Hao</creator><creator>Chen, Xiaoli</creator><creator>Li, Wenge</creator><creator>Lu, Jinxing</creator><creator>Chen, Xiaoping</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20230501</creationdate><title>Establishment of a Fast Diagnostic Method for Sepsis Pathogens Based on M1 Bead Enrichment</title><author>Zheng, Hao ; Chen, Xiaoli ; Li, Wenge ; Lu, Jinxing ; Chen, Xiaoping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-c983274dcd8d5566d8ee2f14e412f19ef8918ebfd21c00965087d035d827d5ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Bacteria</topic><topic>Beads</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Blood</topic><topic>Blood culture</topic><topic>Blood plasma</topic><topic>Candida albicans</topic><topic>Candida tropicalis</topic><topic>Culture</topic><topic>Diagnostic systems</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Humans</topic><topic>lectins</topic><topic>Life Sciences</topic><topic>Low concentrations</topic><topic>magnetism</topic><topic>Mannose</topic><topic>Mannose-binding lectin</topic><topic>Microbiology</topic><topic>Pathogens</topic><topic>Pseudomonas aeruginosa</topic><topic>quantitative polymerase chain reaction</topic><topic>Real time</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Sepsis</topic><topic>Sepsis - diagnosis</topic><topic>Staphylococcal Infections</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - genetics</topic><topic>Streptococcus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Hao</creatorcontrib><creatorcontrib>Chen, Xiaoli</creatorcontrib><creatorcontrib>Li, Wenge</creatorcontrib><creatorcontrib>Lu, Jinxing</creatorcontrib><creatorcontrib>Chen, Xiaoping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</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 Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Current microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Hao</au><au>Chen, Xiaoli</au><au>Li, Wenge</au><au>Lu, Jinxing</au><au>Chen, Xiaoping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment of a Fast Diagnostic Method for Sepsis Pathogens Based on M1 Bead Enrichment</atitle><jtitle>Current microbiology</jtitle><stitle>Curr Microbiol</stitle><addtitle>Curr Microbiol</addtitle><date>2023-05-01</date><risdate>2023</risdate><volume>80</volume><issue>5</issue><spage>166</spage><epage>166</epage><pages>166-166</pages><artnum>166</artnum><issn>0343-8651</issn><eissn>1432-0991</eissn><abstract>Blood culture-based sepsis diagnostic methods usually cannot obtain positive results in a timely manner. Molecular diagnostic methods, such as real-time PCR without blood culture, would be more time-saving and suitable for pathogenic diagnosis of sepsis, while their sensitivities have always been unsatisfactory for the usually low concentration of pathogens in the blood of sepsis patients. In this study, we established a fast diagnostic method using magnetic beads coated with human recombined mannose-binding lectin that makes it possible to concentrate pathogens from human plasma that have low concentrations of pathogens. With subsequent microculture (MC) and real-time PCR, this method allowed the detection of 1–10 CFUs/ml of
Staphylococcus aureus
, Group A
Streptococcus
,
Escherichia coli
,
Pseudomonas aeruginosa
,
Candida tropicalis,
or
C. albicans
from human plasma within 9.5 h, which was 21–80 h earlier than blood culture. The combination of pathogen enrichment and MC made the detection of sepsis-causing pathogens more time-saving and more sensitive than blood culture or real-time PCR alone.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>37022487</pmid><doi>10.1007/s00284-023-03280-6</doi><tpages>1</tpages></addata></record> |
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subjects | Bacteria Beads Biomedical and Life Sciences Biotechnology Blood Blood culture Blood plasma Candida albicans Candida tropicalis Culture Diagnostic systems E coli Escherichia coli Escherichia coli - genetics Humans lectins Life Sciences Low concentrations magnetism Mannose Mannose-binding lectin Microbiology Pathogens Pseudomonas aeruginosa quantitative polymerase chain reaction Real time Real-Time Polymerase Chain Reaction - methods Sepsis Sepsis - diagnosis Staphylococcal Infections Staphylococcus aureus Staphylococcus aureus - genetics Streptococcus |
title | Establishment of a Fast Diagnostic Method for Sepsis Pathogens Based on M1 Bead Enrichment |
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