Multiplex PCR assays developed for neglected pathogen detection in undifferentiated acute febrile illness cases in tropical regions
Undifferentiated acute febrile illness (UAFI) cause by several pathogens poses a diagnostic challenge due to the similarity on the clinical manifestations across these diseases. Precise pathogen detection is vital for appropriate medical intervention, early treatment, and timely outbreak alerts rega...
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creator | Carvajal Aristizabal, Leidi Ciuoderis, Karl Pérez-Restrepo, Laura S Osorio, Jorge E Hernández-Ortiz, Juan P |
description | Undifferentiated acute febrile illness (UAFI) cause by several pathogens poses a diagnostic challenge due to the similarity on the clinical manifestations across these diseases. Precise pathogen detection is vital for appropriate medical intervention, early treatment, and timely outbreak alerts regarding emerging pathogens. In tropical regions, UAFI is predominantly linked to a wide range of viral, bacterial, and parasitic infections. Hence, confirmatory laboratory tests are essential for specific pathogen identification.
Our primary goal was to develop two real-time multiplex polymerase chain reaction (PCR) assays for simultaneous detection of six neglected pathogens (Leptospira spp., Rickettsia spp., Borrelia spp., Anaplasma spp., Brucella spp., and Bartonella spp.), known for causing UAFI in tropical regions.
We rigorously assessed assays parameters including: linearity, efficiency, sensitivity, and reproducibility in both singleplex and multiplex formats.
Our results demonstrated that these multiplex assays are reliable and sensitive methods. They showed good performance with low intra- and inter-variability (< 10%) and consistently high efficiencies (> 90%).
These assays offer the alternative of streamlining work, reducing processing costs, and minimizing sample volume use. In conclusion, we present two dependable, user-friendly, rapid, and cost-effective methods for simultaneously detecting six neglected bacteria, as a significant laboratory tool in resource-limited tropical settings. |
doi_str_mv | 10.1590/0074-02760240053 |
format | Article |
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Our primary goal was to develop two real-time multiplex polymerase chain reaction (PCR) assays for simultaneous detection of six neglected pathogens (Leptospira spp., Rickettsia spp., Borrelia spp., Anaplasma spp., Brucella spp., and Bartonella spp.), known for causing UAFI in tropical regions.
We rigorously assessed assays parameters including: linearity, efficiency, sensitivity, and reproducibility in both singleplex and multiplex formats.
Our results demonstrated that these multiplex assays are reliable and sensitive methods. They showed good performance with low intra- and inter-variability (< 10%) and consistently high efficiencies (> 90%).
These assays offer the alternative of streamlining work, reducing processing costs, and minimizing sample volume use. In conclusion, we present two dependable, user-friendly, rapid, and cost-effective methods for simultaneously detecting six neglected bacteria, as a significant laboratory tool in resource-limited tropical settings.</description><identifier>ISSN: 0074-0276</identifier><identifier>ISSN: 1678-8060</identifier><identifier>EISSN: 1678-8060</identifier><identifier>DOI: 10.1590/0074-02760240053</identifier><identifier>PMID: 39476026</identifier><language>eng</language><publisher>Brazil: Instituto Oswaldo Cruz, Ministério da Saúde</publisher><subject>Acute Disease ; Fever - diagnosis ; Fever - microbiology ; Humans ; Multiplex Polymerase Chain Reaction - methods ; Neglected Diseases - diagnosis ; Neglected Diseases - microbiology ; PARASITOLOGY ; Real-Time Polymerase Chain Reaction - methods ; Reproducibility of Results ; Rickettsia - genetics ; Rickettsia - isolation & purification ; Sensitivity and Specificity ; TROPICAL MEDICINE</subject><ispartof>Memórias do Instituto Oswaldo Cruz, 2024-01, Vol.119, p.e240053</ispartof><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c277t-3c13eff6f91ccdd9c8ba42286aa3e72284d1b53de1a73327e7c4cbe8cd754de33</cites><orcidid>0000-0003-0404-9947</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520662/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11520662/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39476026$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carvajal Aristizabal, Leidi</creatorcontrib><creatorcontrib>Ciuoderis, Karl</creatorcontrib><creatorcontrib>Pérez-Restrepo, Laura S</creatorcontrib><creatorcontrib>Osorio, Jorge E</creatorcontrib><creatorcontrib>Hernández-Ortiz, Juan P</creatorcontrib><title>Multiplex PCR assays developed for neglected pathogen detection in undifferentiated acute febrile illness cases in tropical regions</title><title>Memórias do Instituto Oswaldo Cruz</title><addtitle>Mem Inst Oswaldo Cruz</addtitle><description>Undifferentiated acute febrile illness (UAFI) cause by several pathogens poses a diagnostic challenge due to the similarity on the clinical manifestations across these diseases. Precise pathogen detection is vital for appropriate medical intervention, early treatment, and timely outbreak alerts regarding emerging pathogens. In tropical regions, UAFI is predominantly linked to a wide range of viral, bacterial, and parasitic infections. Hence, confirmatory laboratory tests are essential for specific pathogen identification.
Our primary goal was to develop two real-time multiplex polymerase chain reaction (PCR) assays for simultaneous detection of six neglected pathogens (Leptospira spp., Rickettsia spp., Borrelia spp., Anaplasma spp., Brucella spp., and Bartonella spp.), known for causing UAFI in tropical regions.
We rigorously assessed assays parameters including: linearity, efficiency, sensitivity, and reproducibility in both singleplex and multiplex formats.
Our results demonstrated that these multiplex assays are reliable and sensitive methods. They showed good performance with low intra- and inter-variability (< 10%) and consistently high efficiencies (> 90%).
These assays offer the alternative of streamlining work, reducing processing costs, and minimizing sample volume use. In conclusion, we present two dependable, user-friendly, rapid, and cost-effective methods for simultaneously detecting six neglected bacteria, as a significant laboratory tool in resource-limited tropical settings.</description><subject>Acute Disease</subject><subject>Fever - diagnosis</subject><subject>Fever - microbiology</subject><subject>Humans</subject><subject>Multiplex Polymerase Chain Reaction - methods</subject><subject>Neglected Diseases - diagnosis</subject><subject>Neglected Diseases - microbiology</subject><subject>PARASITOLOGY</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Reproducibility of Results</subject><subject>Rickettsia - genetics</subject><subject>Rickettsia - isolation & purification</subject><subject>Sensitivity and Specificity</subject><subject>TROPICAL MEDICINE</subject><issn>0074-0276</issn><issn>1678-8060</issn><issn>1678-8060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1v1DAQtRCIbgt3TshHLin-SOzsCaFVS5GKQHycLceebF157WA7VXvuH8dhlxU9eTzz3puZNwi9oeScdmvynhDZNoRJQVhLSMefoRUVsm96IshztDqWT9Bpzrekhly0L9EJX7cLR6zQ45fZFzd5uMffNt-xzlk_ZGzhDnycwOIxJhxg68GU-pt0uYlbCBVQasbFgF3Ac7BuHCFBKE4vMG3mAniEITkP2HkfIGdsdIa84EuKkzPa4wTbKpFfoRej9hleH94z9Ovy4ufmqrn--unz5uN1Y5iUpeGGchhHMa6pMdauTT_olrFeaM1B1qC1dOi4Baol50yCNK0ZoDdWdq0Fzs_Q-V43G1fXU7dxTqE2VD8Wo9RiFPtrJKGEUt5Wwoc9YZqHHVhTF0zaqym5nU4PKmqnnlaCu1HbeKco7RgRglWFdweFFH_PkIvauWzAex0gzllxypjgnZR9hZI91KSYc4Lx2IcStVxbHac8XLtS3v4_35Hw77z8D9W4prg</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Carvajal Aristizabal, Leidi</creator><creator>Ciuoderis, Karl</creator><creator>Pérez-Restrepo, Laura S</creator><creator>Osorio, Jorge E</creator><creator>Hernández-Ortiz, Juan P</creator><general>Instituto Oswaldo Cruz, Ministério da Saúde</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>7X8</scope><scope>5PM</scope><scope>GPN</scope><orcidid>https://orcid.org/0000-0003-0404-9947</orcidid></search><sort><creationdate>20240101</creationdate><title>Multiplex PCR assays developed for neglected pathogen detection in undifferentiated acute febrile illness cases in tropical regions</title><author>Carvajal Aristizabal, Leidi ; Ciuoderis, Karl ; Pérez-Restrepo, Laura S ; Osorio, Jorge E ; Hernández-Ortiz, Juan P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c277t-3c13eff6f91ccdd9c8ba42286aa3e72284d1b53de1a73327e7c4cbe8cd754de33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acute Disease</topic><topic>Fever - diagnosis</topic><topic>Fever - microbiology</topic><topic>Humans</topic><topic>Multiplex Polymerase Chain Reaction - methods</topic><topic>Neglected Diseases - diagnosis</topic><topic>Neglected Diseases - microbiology</topic><topic>PARASITOLOGY</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Reproducibility of Results</topic><topic>Rickettsia - genetics</topic><topic>Rickettsia - isolation & purification</topic><topic>Sensitivity and Specificity</topic><topic>TROPICAL MEDICINE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carvajal Aristizabal, Leidi</creatorcontrib><creatorcontrib>Ciuoderis, Karl</creatorcontrib><creatorcontrib>Pérez-Restrepo, Laura S</creatorcontrib><creatorcontrib>Osorio, Jorge E</creatorcontrib><creatorcontrib>Hernández-Ortiz, Juan P</creatorcontrib><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><collection>SciELO</collection><jtitle>Memórias do Instituto Oswaldo Cruz</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carvajal Aristizabal, Leidi</au><au>Ciuoderis, Karl</au><au>Pérez-Restrepo, Laura S</au><au>Osorio, Jorge E</au><au>Hernández-Ortiz, Juan P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiplex PCR assays developed for neglected pathogen detection in undifferentiated acute febrile illness cases in tropical regions</atitle><jtitle>Memórias do Instituto Oswaldo Cruz</jtitle><addtitle>Mem Inst Oswaldo Cruz</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>119</volume><spage>e240053</spage><pages>e240053-</pages><issn>0074-0276</issn><issn>1678-8060</issn><eissn>1678-8060</eissn><abstract>Undifferentiated acute febrile illness (UAFI) cause by several pathogens poses a diagnostic challenge due to the similarity on the clinical manifestations across these diseases. Precise pathogen detection is vital for appropriate medical intervention, early treatment, and timely outbreak alerts regarding emerging pathogens. In tropical regions, UAFI is predominantly linked to a wide range of viral, bacterial, and parasitic infections. Hence, confirmatory laboratory tests are essential for specific pathogen identification.
Our primary goal was to develop two real-time multiplex polymerase chain reaction (PCR) assays for simultaneous detection of six neglected pathogens (Leptospira spp., Rickettsia spp., Borrelia spp., Anaplasma spp., Brucella spp., and Bartonella spp.), known for causing UAFI in tropical regions.
We rigorously assessed assays parameters including: linearity, efficiency, sensitivity, and reproducibility in both singleplex and multiplex formats.
Our results demonstrated that these multiplex assays are reliable and sensitive methods. They showed good performance with low intra- and inter-variability (< 10%) and consistently high efficiencies (> 90%).
These assays offer the alternative of streamlining work, reducing processing costs, and minimizing sample volume use. In conclusion, we present two dependable, user-friendly, rapid, and cost-effective methods for simultaneously detecting six neglected bacteria, as a significant laboratory tool in resource-limited tropical settings.</abstract><cop>Brazil</cop><pub>Instituto Oswaldo Cruz, Ministério da Saúde</pub><pmid>39476026</pmid><doi>10.1590/0074-02760240053</doi><orcidid>https://orcid.org/0000-0003-0404-9947</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Fever - diagnosis Fever - microbiology Humans Multiplex Polymerase Chain Reaction - methods Neglected Diseases - diagnosis Neglected Diseases - microbiology PARASITOLOGY Real-Time Polymerase Chain Reaction - methods Reproducibility of Results Rickettsia - genetics Rickettsia - isolation & purification Sensitivity and Specificity TROPICAL MEDICINE |
title | Multiplex PCR assays developed for neglected pathogen detection in undifferentiated acute febrile illness cases in tropical regions |
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