Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness
One hundred and eighty febrile patients were analyzed in a prospective evaluation of Orientia tsutsugamushi and Rickettsia spp. real-time polymerase chain reaction (PCR) assays for early diagnosis of rickettsial infections. By paired serology, 3.9% (7 of 180) and 6.1% (11 of 180) of patients were co...
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th-mahidol.318942018-10-19T12:20:21Z Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness Wanitda Watthanaworawit Paul Turner Claudia Turner Ampai Tanganuchitcharnchai Allen L. Richards Kevin M. Bourzac Stuart D. Blacksell François Nosten Shoklo Malaria Research Unit Mahidol University University of Oxford Naval Medical Research Center BioFire Diagnostics, LLC Immunology and Microbiology Medicine One hundred and eighty febrile patients were analyzed in a prospective evaluation of Orientia tsutsugamushi and Rickettsia spp. real-time polymerase chain reaction (PCR) assays for early diagnosis of rickettsial infections. By paired serology, 3.9% (7 of 180) and 6.1% (11 of 180) of patients were confirmed to have acute scrub or murine typhus, respectively. The PCR assays for the detection of O. tsutsugamushi and Rickettsia spp. had high specificity (99.4% [95% confidence interval (CI): 96.8-100] and 100%[95%CI: 97.8-100], respectively). The PCR results were also compared with immunoglobulinM(IgM) immunofluorescence assay (IFA) on acute sera. For O. tsutsugamushi, PCR sensitivity was twice that of acute specimen IgM IFA (28.6% versus 14.3%; McNemar's P = 0.3). For Rickettsia spp., PCR was four times as sensitive as acute specimen IgM IFA (36.4% versus 9.1%; P = 0.08), although this was not statistically significant. Whole blood and buffy coat, but not serum, were acceptable specimens for these PCRs. Further evaluation of these assays in a larger prospective study is warranted. Copyright © 2013 by The American Society of Tropical Medicine and Hygiene. 2018-10-19T05:02:34Z 2018-10-19T05:02:34Z 2013-08-01 Article American Journal of Tropical Medicine and Hygiene. Vol.89, No.2 (2013), 308-310 10.4269/ajtmh.12-0600 00029637 2-s2.0-84881513987 https://repository.li.mahidol.ac.th/handle/123456789/31894 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84881513987&origin=inward |
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Immunology and Microbiology Medicine Wanitda Watthanaworawit Paul Turner Claudia Turner Ampai Tanganuchitcharnchai Allen L. Richards Kevin M. Bourzac Stuart D. Blacksell François Nosten Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
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One hundred and eighty febrile patients were analyzed in a prospective evaluation of Orientia tsutsugamushi and Rickettsia spp. real-time polymerase chain reaction (PCR) assays for early diagnosis of rickettsial infections. By paired serology, 3.9% (7 of 180) and 6.1% (11 of 180) of patients were confirmed to have acute scrub or murine typhus, respectively. The PCR assays for the detection of O. tsutsugamushi and Rickettsia spp. had high specificity (99.4% [95% confidence interval (CI): 96.8-100] and 100%[95%CI: 97.8-100], respectively). The PCR results were also compared with immunoglobulinM(IgM) immunofluorescence assay (IFA) on acute sera. For O. tsutsugamushi, PCR sensitivity was twice that of acute specimen IgM IFA (28.6% versus 14.3%; McNemar's P = 0.3). For Rickettsia spp., PCR was four times as sensitive as acute specimen IgM IFA (36.4% versus 9.1%; P = 0.08), although this was not statistically significant. Whole blood and buffy coat, but not serum, were acceptable specimens for these PCRs. Further evaluation of these assays in a larger prospective study is warranted. Copyright © 2013 by The American Society of Tropical Medicine and Hygiene. |
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Shoklo Malaria Research Unit |
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Shoklo Malaria Research Unit Wanitda Watthanaworawit Paul Turner Claudia Turner Ampai Tanganuchitcharnchai Allen L. Richards Kevin M. Bourzac Stuart D. Blacksell François Nosten |
format |
Article |
author |
Wanitda Watthanaworawit Paul Turner Claudia Turner Ampai Tanganuchitcharnchai Allen L. Richards Kevin M. Bourzac Stuart D. Blacksell François Nosten |
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Wanitda Watthanaworawit |
title |
Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
title_short |
Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
title_full |
Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
title_fullStr |
Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
title_full_unstemmed |
Short report: A prospective evaluation of real-time PCR assays for the detection of Orientia tsutsugamushi and Rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
title_sort |
short report: a prospective evaluation of real-time pcr assays for the detection of orientia tsutsugamushi and rickettsia spp. for early diagnosis of rickettsial infections during the acute phase of undifferentiated febrile illness |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/31894 |
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1763494318623948800 |