Development of Recombinase Polymerase Amplification Assays for Detection of Orientia tsutsugamushi or Rickettsia typhi
Sensitive, specific and rapid diagnostic tests for the detection of Orientia tsutsugamushi (O. tsutsugamushi) and Rickettsia typhi (R. typhi), the causative agents of scrub typhus and murine typhus, respectively, are necessary to accurately and promptly diagnose patients and ensure that they receive...
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description | Sensitive, specific and rapid diagnostic tests for the detection of Orientia tsutsugamushi (O. tsutsugamushi) and Rickettsia typhi (R. typhi), the causative agents of scrub typhus and murine typhus, respectively, are necessary to accurately and promptly diagnose patients and ensure that they receive proper treatment. Recombinase polymerase amplification (RPA) assays using a lateral flow test (RPA-nfo) and real-time fluorescent detection (RPA-exo) were developed targeting the 47-kDa gene of O. tsutsugamushi or 17 kDa gene of R. typhi. The RPA assay was capable of detecting O. tsutsugamushi or R. typhi at levels comparable to that of the quantitative PCR method. Both the RPA-nfo and RPA-exo methods performed similarly with regards to sensitivity when detecting the 17 kDa gene of R. typhi. On the contrary, RPA-exo performed better than RPA-nfo in detecting the 47 kDa gene of O. tsutsugamushi. The clinical performance of the O. tsutsugamushi RPA assay was evaluated using either human patient samples or infected mouse samples. Eight out of ten PCR confirmed positives were determined positive by RPA, and all PCR confirmed negative samples were negative by RPA. Similar results were obtained for R. typhi spiked patient sera. The assays were able to differentiate O. tsutsugamushi and R. typhi from other phylogenetically related bacteria as well as mouse and human DNA. Furthermore, the RPA-nfo reaction was completed in 20 minutes at 37°C followed by a 10 minute incubation at room temperature for development of an immunochromatographic strip. The RPA-exo reaction was completed in 20 minutes at 39°C. The implementation of a cross contamination proof cassette to detect the RPA-nfo fluorescent amplicons provided an alternative to regular lateral flow detection strips, which are more prone to cross contamination. The RPA assays provide a highly time-efficient, sensitive and specific alternative to other methods for diagnosing scrub typhus or murine typhus. |
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Recombinase polymerase amplification (RPA) assays using a lateral flow test (RPA-nfo) and real-time fluorescent detection (RPA-exo) were developed targeting the 47-kDa gene of O. tsutsugamushi or 17 kDa gene of R. typhi. The RPA assay was capable of detecting O. tsutsugamushi or R. typhi at levels comparable to that of the quantitative PCR method. Both the RPA-nfo and RPA-exo methods performed similarly with regards to sensitivity when detecting the 17 kDa gene of R. typhi. On the contrary, RPA-exo performed better than RPA-nfo in detecting the 47 kDa gene of O. tsutsugamushi. The clinical performance of the O. tsutsugamushi RPA assay was evaluated using either human patient samples or infected mouse samples. Eight out of ten PCR confirmed positives were determined positive by RPA, and all PCR confirmed negative samples were negative by RPA. Similar results were obtained for R. typhi spiked patient sera. The assays were able to differentiate O. tsutsugamushi and R. typhi from other phylogenetically related bacteria as well as mouse and human DNA. Furthermore, the RPA-nfo reaction was completed in 20 minutes at 37°C followed by a 10 minute incubation at room temperature for development of an immunochromatographic strip. The RPA-exo reaction was completed in 20 minutes at 39°C. The implementation of a cross contamination proof cassette to detect the RPA-nfo fluorescent amplicons provided an alternative to regular lateral flow detection strips, which are more prone to cross contamination. The RPA assays provide a highly time-efficient, sensitive and specific alternative to other methods for diagnosing scrub typhus or murine typhus.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0003884</identifier><identifier>PMID: 26161793</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Antigens ; Copyright ; Deoxyribonucleic acid ; DNA ; Fever ; Genetic testing ; Humans ; Infections ; Laboratories ; Methods ; Mice ; Mortality ; Orientia tsutsugamushi ; Orientia tsutsugamushi - genetics ; Orientia tsutsugamushi - isolation & purification ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Recombinases - metabolism ; Rickettsia typhi ; Rickettsia typhi - genetics ; Rickettsia typhi - isolation & purification ; Scrub Typhus - diagnosis ; Scrub Typhus - microbiology ; Sensitivity and Specificity ; Tropical diseases ; Typhus ; Typhus, Endemic Flea-Borne - diagnosis ; Typhus, Endemic Flea-Borne - microbiology ; User training</subject><ispartof>PLoS neglected tropical diseases, 2015, Vol.9 (7), p.e0003884-e0003884</ispartof><rights>2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: . PLoS Negl Trop Dis 9(7): e0003884. doi:10.1371/journal.pntd.0003884</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-99e93fb9eccae1d3e364f26dee4f51b15f170be3d55ca3c1ba94c630e88f67f63</citedby><cites>FETCH-LOGICAL-c531t-99e93fb9eccae1d3e364f26dee4f51b15f170be3d55ca3c1ba94c630e88f67f63</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/PMC4498641/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498641/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,4022,23865,27922,27923,27924,53790,53792,79371,79372</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26161793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Raoult, Didier</contributor><creatorcontrib>Chao, Chien-Chung</creatorcontrib><creatorcontrib>Belinskaya, Tatyana</creatorcontrib><creatorcontrib>Zhang, Zhiwen</creatorcontrib><creatorcontrib>Ching, Wei-Mei</creatorcontrib><title>Development of Recombinase Polymerase Amplification Assays for Detection of Orientia tsutsugamushi or Rickettsia typhi</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Sensitive, specific and rapid diagnostic tests for the detection of Orientia tsutsugamushi (O. tsutsugamushi) and Rickettsia typhi (R. typhi), the causative agents of scrub typhus and murine typhus, respectively, are necessary to accurately and promptly diagnose patients and ensure that they receive proper treatment. Recombinase polymerase amplification (RPA) assays using a lateral flow test (RPA-nfo) and real-time fluorescent detection (RPA-exo) were developed targeting the 47-kDa gene of O. tsutsugamushi or 17 kDa gene of R. typhi. The RPA assay was capable of detecting O. tsutsugamushi or R. typhi at levels comparable to that of the quantitative PCR method. Both the RPA-nfo and RPA-exo methods performed similarly with regards to sensitivity when detecting the 17 kDa gene of R. typhi. On the contrary, RPA-exo performed better than RPA-nfo in detecting the 47 kDa gene of O. tsutsugamushi. The clinical performance of the O. tsutsugamushi RPA assay was evaluated using either human patient samples or infected mouse samples. Eight out of ten PCR confirmed positives were determined positive by RPA, and all PCR confirmed negative samples were negative by RPA. Similar results were obtained for R. typhi spiked patient sera. The assays were able to differentiate O. tsutsugamushi and R. typhi from other phylogenetically related bacteria as well as mouse and human DNA. Furthermore, the RPA-nfo reaction was completed in 20 minutes at 37°C followed by a 10 minute incubation at room temperature for development of an immunochromatographic strip. The RPA-exo reaction was completed in 20 minutes at 39°C. The implementation of a cross contamination proof cassette to detect the RPA-nfo fluorescent amplicons provided an alternative to regular lateral flow detection strips, which are more prone to cross contamination. The RPA assays provide a highly time-efficient, sensitive and specific alternative to other methods for diagnosing scrub typhus or murine typhus.</description><subject>Animals</subject><subject>Antigens</subject><subject>Copyright</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Fever</subject><subject>Genetic testing</subject><subject>Humans</subject><subject>Infections</subject><subject>Laboratories</subject><subject>Methods</subject><subject>Mice</subject><subject>Mortality</subject><subject>Orientia tsutsugamushi</subject><subject>Orientia tsutsugamushi - genetics</subject><subject>Orientia tsutsugamushi - isolation & purification</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Recombinases - metabolism</subject><subject>Rickettsia typhi</subject><subject>Rickettsia typhi - genetics</subject><subject>Rickettsia typhi - isolation & purification</subject><subject>Scrub Typhus - diagnosis</subject><subject>Scrub Typhus - microbiology</subject><subject>Sensitivity and Specificity</subject><subject>Tropical diseases</subject><subject>Typhus</subject><subject>Typhus, Endemic Flea-Borne - diagnosis</subject><subject>Typhus, Endemic Flea-Borne - microbiology</subject><subject>User training</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqFUl1r2zAUNWNj_dj-wdj8uJdkkmVJ1ssgtFtXKHSU7VnI8lWiTLY8SQ7k309O0tI-DQS63HvO0dHlFMUHjJaYcPxl66cwKLcch9QtEUKkaepXxTkWhC4qTujrZ_VZcRHjFiEqaIPfFmcVwwxzQc6L3TXswPmxhyGV3pQPoH3f2kFFKH96t-8hzOWqH501Vqtk_VCuYlT7WBofymtIoA_NTL4PNstYVaY45bNW_RQ3tsywB6v_QEpxnu3HjX1XvDHKRXh_ui-L39-__br6sbi7v7m9Wt0tNCU4LYQAQUwrQGsFuCNAWG0q1gHUhuIWU4M5aoF0lGpFNG6VqDUjCJrGMG4YuSw-HXVH56M8rSzKzKKINayuMuL2iOi82sox2F6FvfTKykPDh7VUIVntQHJeUVxpIkRH64oRUSGuOFW6I8JAO2t9Pb02tT10Oi8jKPdC9OVksBu59jtZ1yKbwVng80kg-L8TxCR7GzU4pwbw08G3wLzCRPwfygTDAmEy26qPUB18jAHMkyOM5Jylx8XIOUvylKVM-_j8N0-kx_CQf2onyxw</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Chao, Chien-Chung</creator><creator>Belinskaya, Tatyana</creator><creator>Zhang, Zhiwen</creator><creator>Ching, Wei-Mei</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>7QL</scope><scope>C1K</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>2015</creationdate><title>Development of Recombinase Polymerase Amplification Assays for Detection of Orientia tsutsugamushi or Rickettsia typhi</title><author>Chao, Chien-Chung ; Belinskaya, Tatyana ; Zhang, Zhiwen ; Ching, Wei-Mei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-99e93fb9eccae1d3e364f26dee4f51b15f170be3d55ca3c1ba94c630e88f67f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Antigens</topic><topic>Copyright</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Fever</topic><topic>Genetic testing</topic><topic>Humans</topic><topic>Infections</topic><topic>Laboratories</topic><topic>Methods</topic><topic>Mice</topic><topic>Mortality</topic><topic>Orientia tsutsugamushi</topic><topic>Orientia tsutsugamushi - genetics</topic><topic>Orientia tsutsugamushi - isolation & purification</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Recombinases - metabolism</topic><topic>Rickettsia typhi</topic><topic>Rickettsia typhi - genetics</topic><topic>Rickettsia typhi - isolation & purification</topic><topic>Scrub Typhus - diagnosis</topic><topic>Scrub Typhus - microbiology</topic><topic>Sensitivity and Specificity</topic><topic>Tropical diseases</topic><topic>Typhus</topic><topic>Typhus, Endemic Flea-Borne - diagnosis</topic><topic>Typhus, Endemic Flea-Borne - microbiology</topic><topic>User training</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chao, Chien-Chung</creatorcontrib><creatorcontrib>Belinskaya, Tatyana</creatorcontrib><creatorcontrib>Zhang, Zhiwen</creatorcontrib><creatorcontrib>Ching, Wei-Mei</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chao, Chien-Chung</au><au>Belinskaya, Tatyana</au><au>Zhang, Zhiwen</au><au>Ching, Wei-Mei</au><au>Raoult, Didier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of Recombinase Polymerase Amplification Assays for Detection of Orientia tsutsugamushi or Rickettsia typhi</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2015</date><risdate>2015</risdate><volume>9</volume><issue>7</issue><spage>e0003884</spage><epage>e0003884</epage><pages>e0003884-e0003884</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Sensitive, specific and rapid diagnostic tests for the detection of Orientia tsutsugamushi (O. tsutsugamushi) and Rickettsia typhi (R. typhi), the causative agents of scrub typhus and murine typhus, respectively, are necessary to accurately and promptly diagnose patients and ensure that they receive proper treatment. Recombinase polymerase amplification (RPA) assays using a lateral flow test (RPA-nfo) and real-time fluorescent detection (RPA-exo) were developed targeting the 47-kDa gene of O. tsutsugamushi or 17 kDa gene of R. typhi. The RPA assay was capable of detecting O. tsutsugamushi or R. typhi at levels comparable to that of the quantitative PCR method. Both the RPA-nfo and RPA-exo methods performed similarly with regards to sensitivity when detecting the 17 kDa gene of R. typhi. On the contrary, RPA-exo performed better than RPA-nfo in detecting the 47 kDa gene of O. tsutsugamushi. The clinical performance of the O. tsutsugamushi RPA assay was evaluated using either human patient samples or infected mouse samples. Eight out of ten PCR confirmed positives were determined positive by RPA, and all PCR confirmed negative samples were negative by RPA. Similar results were obtained for R. typhi spiked patient sera. The assays were able to differentiate O. tsutsugamushi and R. typhi from other phylogenetically related bacteria as well as mouse and human DNA. Furthermore, the RPA-nfo reaction was completed in 20 minutes at 37°C followed by a 10 minute incubation at room temperature for development of an immunochromatographic strip. The RPA-exo reaction was completed in 20 minutes at 39°C. The implementation of a cross contamination proof cassette to detect the RPA-nfo fluorescent amplicons provided an alternative to regular lateral flow detection strips, which are more prone to cross contamination. The RPA assays provide a highly time-efficient, sensitive and specific alternative to other methods for diagnosing scrub typhus or murine typhus.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26161793</pmid><doi>10.1371/journal.pntd.0003884</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens Copyright Deoxyribonucleic acid DNA Fever Genetic testing Humans Infections Laboratories Methods Mice Mortality Orientia tsutsugamushi Orientia tsutsugamushi - genetics Orientia tsutsugamushi - isolation & purification Polymerase chain reaction Polymerase Chain Reaction - methods Recombinases - metabolism Rickettsia typhi Rickettsia typhi - genetics Rickettsia typhi - isolation & purification Scrub Typhus - diagnosis Scrub Typhus - microbiology Sensitivity and Specificity Tropical diseases Typhus Typhus, Endemic Flea-Borne - diagnosis Typhus, Endemic Flea-Borne - microbiology User training |
title | Development of Recombinase Polymerase Amplification Assays for Detection of Orientia tsutsugamushi or Rickettsia typhi |
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