Combined PCR and MAT improves the early diagnosis of the biphasic illness leptospirosis
The diagnosis of leptospirosis remains a challenge due to its non-specific symptoms and the biphasic nature of the illness. A comprehensive diagnosis that includes both molecular (polymerase chain reaction (PCR)) and serology is vital for early detection of leptospirosis and to avoid misdiagnosis. H...
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description | The diagnosis of leptospirosis remains a challenge due to its non-specific symptoms and the biphasic nature of the illness. A comprehensive diagnosis that includes both molecular (polymerase chain reaction (PCR)) and serology is vital for early detection of leptospirosis and to avoid misdiagnosis. However, not all samples could be subjected to both tests (serology and molecular) due to budget limitation, infrastructure, and technical expertise at least in resource-limited countries. We evaluated the usefulness of testing the clinically suspected leptospirosis cases with both techniques on all samples collected from the patients on the day of admission. Among the 165 patient's blood/serum samples tested (from three hospitals in Central Malaysia), 43 (26%) showed positivity by microscopic agglutination test (MAT), 63 (38%) by PCR, while 14 (8%) were positive by both MAT and PCR. For PCR, we tested two molecular targets (lipL32 by qPCR and 16S rDNA or rrs by nested PCR) and detected lipL32 in 47 (29%) and rrs gene in 63 (38%) patients. The use of more than one target gene for PCR increased the detection rates. Hence, a highly sensitive multiplex PCR targeting more than one diagnostic marker is recommended for the early detection of Leptospira in suspected patients. When the frequencies for positivity detected either by MAT or PCR combined, leptospirosis was diagnosed in a total of 92 (56%) patients, a higher frequency compared to when samples were only tested by a single method (MAT or PCR). The results from this study suggest the inclusion of both serology and molecular methods for every first sample irrespective of the days post-onset of symptoms (DPO) collected from patients for early diagnosis of leptospirosis. |
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A comprehensive diagnosis that includes both molecular (polymerase chain reaction (PCR)) and serology is vital for early detection of leptospirosis and to avoid misdiagnosis. However, not all samples could be subjected to both tests (serology and molecular) due to budget limitation, infrastructure, and technical expertise at least in resource-limited countries. We evaluated the usefulness of testing the clinically suspected leptospirosis cases with both techniques on all samples collected from the patients on the day of admission. Among the 165 patient's blood/serum samples tested (from three hospitals in Central Malaysia), 43 (26%) showed positivity by microscopic agglutination test (MAT), 63 (38%) by PCR, while 14 (8%) were positive by both MAT and PCR. For PCR, we tested two molecular targets (lipL32 by qPCR and 16S rDNA or rrs by nested PCR) and detected lipL32 in 47 (29%) and rrs gene in 63 (38%) patients. The use of more than one target gene for PCR increased the detection rates. Hence, a highly sensitive multiplex PCR targeting more than one diagnostic marker is recommended for the early detection of Leptospira in suspected patients. When the frequencies for positivity detected either by MAT or PCR combined, leptospirosis was diagnosed in a total of 92 (56%) patients, a higher frequency compared to when samples were only tested by a single method (MAT or PCR). The results from this study suggest the inclusion of both serology and molecular methods for every first sample irrespective of the days post-onset of symptoms (DPO) collected from patients for early diagnosis of leptospirosis.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0239069</identifier><identifier>PMID: 32915919</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Agglutination ; Agglutination tests ; Biology and Life Sciences ; Deoxyribonucleic acid ; Diagnosis ; Diagnostic systems ; Disease ; DNA ; Funding ; Health sciences ; Hospitals ; Illnesses ; Leptospirosis ; Medical diagnosis ; Medical research ; Medicine ; Medicine and Health Sciences ; Methods ; Microscopy ; Molecular chains ; Parasitology ; People and Places ; Polymerase chain reaction ; Research and Analysis Methods ; rRNA 16S ; Rrs gene ; Sepsis ; Serology ; Urine</subject><ispartof>PloS one, 2020-09, Vol.15 (9), p.e0239069-e0239069</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Philip et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Philip et al 2020 Philip et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c669t-861033da5ba34bbedae81b252b675aa0e6308a42c8e2e6383f2a830d71ee208e3</citedby><cites>FETCH-LOGICAL-c669t-861033da5ba34bbedae81b252b675aa0e6308a42c8e2e6383f2a830d71ee208e3</cites><orcidid>0000-0002-3917-6316</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/PMC7485768/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485768/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids></links><search><creatorcontrib>Philip, Noraini</creatorcontrib><creatorcontrib>Affendy, Norliza Bahtiar</creatorcontrib><creatorcontrib>Masri, Siti Norbaya</creatorcontrib><creatorcontrib>Yuhana, Muhamad Yazli</creatorcontrib><creatorcontrib>Than, Leslie Thian Lung</creatorcontrib><creatorcontrib>Sekawi, Zamberi</creatorcontrib><creatorcontrib>Neela, Vasantha Kumari</creatorcontrib><title>Combined PCR and MAT improves the early diagnosis of the biphasic illness leptospirosis</title><title>PloS one</title><description>The diagnosis of leptospirosis remains a challenge due to its non-specific symptoms and the biphasic nature of the illness. A comprehensive diagnosis that includes both molecular (polymerase chain reaction (PCR)) and serology is vital for early detection of leptospirosis and to avoid misdiagnosis. However, not all samples could be subjected to both tests (serology and molecular) due to budget limitation, infrastructure, and technical expertise at least in resource-limited countries. We evaluated the usefulness of testing the clinically suspected leptospirosis cases with both techniques on all samples collected from the patients on the day of admission. Among the 165 patient's blood/serum samples tested (from three hospitals in Central Malaysia), 43 (26%) showed positivity by microscopic agglutination test (MAT), 63 (38%) by PCR, while 14 (8%) were positive by both MAT and PCR. For PCR, we tested two molecular targets (lipL32 by qPCR and 16S rDNA or rrs by nested PCR) and detected lipL32 in 47 (29%) and rrs gene in 63 (38%) patients. The use of more than one target gene for PCR increased the detection rates. Hence, a highly sensitive multiplex PCR targeting more than one diagnostic marker is recommended for the early detection of Leptospira in suspected patients. When the frequencies for positivity detected either by MAT or PCR combined, leptospirosis was diagnosed in a total of 92 (56%) patients, a higher frequency compared to when samples were only tested by a single method (MAT or PCR). The results from this study suggest the inclusion of both serology and molecular methods for every first sample irrespective of the days post-onset of symptoms (DPO) collected from patients for early diagnosis of leptospirosis.</description><subject>Agglutination</subject><subject>Agglutination tests</subject><subject>Biology and Life Sciences</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>Diagnostic systems</subject><subject>Disease</subject><subject>DNA</subject><subject>Funding</subject><subject>Health sciences</subject><subject>Hospitals</subject><subject>Illnesses</subject><subject>Leptospirosis</subject><subject>Medical diagnosis</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Microscopy</subject><subject>Molecular chains</subject><subject>Parasitology</subject><subject>People and Places</subject><subject>Polymerase chain 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PCR and MAT improves the early diagnosis of the biphasic illness leptospirosis</title><author>Philip, Noraini ; Affendy, Norliza Bahtiar ; Masri, Siti Norbaya ; Yuhana, Muhamad Yazli ; Than, Leslie Thian Lung ; Sekawi, Zamberi ; Neela, Vasantha Kumari</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c669t-861033da5ba34bbedae81b252b675aa0e6308a42c8e2e6383f2a830d71ee208e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Agglutination</topic><topic>Agglutination tests</topic><topic>Biology and Life Sciences</topic><topic>Deoxyribonucleic acid</topic><topic>Diagnosis</topic><topic>Diagnostic systems</topic><topic>Disease</topic><topic>DNA</topic><topic>Funding</topic><topic>Health sciences</topic><topic>Hospitals</topic><topic>Illnesses</topic><topic>Leptospirosis</topic><topic>Medical diagnosis</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine and 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one</jtitle><date>2020-09-11</date><risdate>2020</risdate><volume>15</volume><issue>9</issue><spage>e0239069</spage><epage>e0239069</epage><pages>e0239069-e0239069</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The diagnosis of leptospirosis remains a challenge due to its non-specific symptoms and the biphasic nature of the illness. A comprehensive diagnosis that includes both molecular (polymerase chain reaction (PCR)) and serology is vital for early detection of leptospirosis and to avoid misdiagnosis. However, not all samples could be subjected to both tests (serology and molecular) due to budget limitation, infrastructure, and technical expertise at least in resource-limited countries. We evaluated the usefulness of testing the clinically suspected leptospirosis cases with both techniques on all samples collected from the patients on the day of admission. Among the 165 patient's blood/serum samples tested (from three hospitals in Central Malaysia), 43 (26%) showed positivity by microscopic agglutination test (MAT), 63 (38%) by PCR, while 14 (8%) were positive by both MAT and PCR. For PCR, we tested two molecular targets (lipL32 by qPCR and 16S rDNA or rrs by nested PCR) and detected lipL32 in 47 (29%) and rrs gene in 63 (38%) patients. The use of more than one target gene for PCR increased the detection rates. Hence, a highly sensitive multiplex PCR targeting more than one diagnostic marker is recommended for the early detection of Leptospira in suspected patients. When the frequencies for positivity detected either by MAT or PCR combined, leptospirosis was diagnosed in a total of 92 (56%) patients, a higher frequency compared to when samples were only tested by a single method (MAT or PCR). The results from this study suggest the inclusion of both serology and molecular methods for every first sample irrespective of the days post-onset of symptoms (DPO) collected from patients for early diagnosis of leptospirosis.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>32915919</pmid><doi>10.1371/journal.pone.0239069</doi><tpages>e0239069</tpages><orcidid>https://orcid.org/0000-0002-3917-6316</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Agglutination Agglutination tests Biology and Life Sciences Deoxyribonucleic acid Diagnosis Diagnostic systems Disease DNA Funding Health sciences Hospitals Illnesses Leptospirosis Medical diagnosis Medical research Medicine Medicine and Health Sciences Methods Microscopy Molecular chains Parasitology People and Places Polymerase chain reaction Research and Analysis Methods rRNA 16S Rrs gene Sepsis Serology Urine |
title | Combined PCR and MAT improves the early diagnosis of the biphasic illness leptospirosis |
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