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Leptospirosis infections among hospital patients, Sarawak, Malaysia
BACKGROUND: Leptospirosis diagnoses have increased in Sarawak, Malaysia in recent years. METHODS: To better understand the burden of disease and associated risk factors, we evaluated 147 patients presenting with clinical leptospirosis to local hospitals in Sarawak, Malaysia for the presence of Lepto...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559352/ https://www.ncbi.nlm.nih.gov/pubmed/34719397 http://dx.doi.org/10.1186/s40794-021-00154-2 |
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author | Hii, King-Ching Robie, Emily R. Saihidi, Izreena Berita, Antoinette Alarja, Natalie A. Xiu, Leshan Merchant, James A. Binder, Raquel A. Goh, Johnny Keh-Tun Guernier-Cambert, Vanina Galán, Diego Gregory, Michael J. Gray, Gregory C. |
author_facet | Hii, King-Ching Robie, Emily R. Saihidi, Izreena Berita, Antoinette Alarja, Natalie A. Xiu, Leshan Merchant, James A. Binder, Raquel A. Goh, Johnny Keh-Tun Guernier-Cambert, Vanina Galán, Diego Gregory, Michael J. Gray, Gregory C. |
author_sort | Hii, King-Ching |
collection | PubMed |
description | BACKGROUND: Leptospirosis diagnoses have increased in Sarawak, Malaysia in recent years. METHODS: To better understand the burden of disease and associated risk factors, we evaluated 147 patients presenting with clinical leptospirosis to local hospitals in Sarawak, Malaysia for the presence of Leptospira and associated antibodies. Sera and urine specimens collected during the acute illness phase were assessed via a commercially available rapid diagnostic test (Leptorapide, Linnodee Ltd., Antrim, Northern Ireland), an ELISA IgM assay (Leptospira IgM ELISA, PanBio, Queensland, Australia) and a pan-Leptospira real-time PCR (qPCR) assay to estimate disease prevalence and diagnostic accuracy of each method. Microagglutination testing was performed on a subset of samples. RESULTS: Overall, 45 out of 147 patients (30.6%) showed evidence of leptospires through qPCR in either one or both sera (20 patients) or urine (33 patients), and an additional ten (6.8%) were considered positive through serological testing, for an overall prevalence of 37.4% within the study population. However, each diagnostic method individually yielded disparate prevalence estimates: rapid test 42.2% for sera and 30.5% for urine, ELISA 15.0% for sera, qPCR 13.8% for sera and 23.4% for urine. Molecular characterization of a subset of positive samples by conventional PCR identified the bacterial species as Leptospira interrogans in 4 specimens. A multivariate risk factor analysis for the outcome of leptospirosis identified having completed primary school (OR = 2.5; 95 CI% 1.0–6.4) and weekly clothes-washing in local rivers (OR = 10.6; 95 CI% 1.4–214.8) with increased likelihood of leptospirosis when compared with those who had not. CONCLUSION: Overall, the data suggest a relatively high prevalence of leptospirosis in the study population. The low sensitivities of the rapid diagnostic test and ELISA assay against qPCR highlight a need for better screening tools. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40794-021-00154-2. |
format | Online Article Text |
id | pubmed-8559352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85593522021-11-03 Leptospirosis infections among hospital patients, Sarawak, Malaysia Hii, King-Ching Robie, Emily R. Saihidi, Izreena Berita, Antoinette Alarja, Natalie A. Xiu, Leshan Merchant, James A. Binder, Raquel A. Goh, Johnny Keh-Tun Guernier-Cambert, Vanina Galán, Diego Gregory, Michael J. Gray, Gregory C. Trop Dis Travel Med Vaccines Research BACKGROUND: Leptospirosis diagnoses have increased in Sarawak, Malaysia in recent years. METHODS: To better understand the burden of disease and associated risk factors, we evaluated 147 patients presenting with clinical leptospirosis to local hospitals in Sarawak, Malaysia for the presence of Leptospira and associated antibodies. Sera and urine specimens collected during the acute illness phase were assessed via a commercially available rapid diagnostic test (Leptorapide, Linnodee Ltd., Antrim, Northern Ireland), an ELISA IgM assay (Leptospira IgM ELISA, PanBio, Queensland, Australia) and a pan-Leptospira real-time PCR (qPCR) assay to estimate disease prevalence and diagnostic accuracy of each method. Microagglutination testing was performed on a subset of samples. RESULTS: Overall, 45 out of 147 patients (30.6%) showed evidence of leptospires through qPCR in either one or both sera (20 patients) or urine (33 patients), and an additional ten (6.8%) were considered positive through serological testing, for an overall prevalence of 37.4% within the study population. However, each diagnostic method individually yielded disparate prevalence estimates: rapid test 42.2% for sera and 30.5% for urine, ELISA 15.0% for sera, qPCR 13.8% for sera and 23.4% for urine. Molecular characterization of a subset of positive samples by conventional PCR identified the bacterial species as Leptospira interrogans in 4 specimens. A multivariate risk factor analysis for the outcome of leptospirosis identified having completed primary school (OR = 2.5; 95 CI% 1.0–6.4) and weekly clothes-washing in local rivers (OR = 10.6; 95 CI% 1.4–214.8) with increased likelihood of leptospirosis when compared with those who had not. CONCLUSION: Overall, the data suggest a relatively high prevalence of leptospirosis in the study population. The low sensitivities of the rapid diagnostic test and ELISA assay against qPCR highlight a need for better screening tools. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40794-021-00154-2. BioMed Central 2021-11-01 /pmc/articles/PMC8559352/ /pubmed/34719397 http://dx.doi.org/10.1186/s40794-021-00154-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hii, King-Ching Robie, Emily R. Saihidi, Izreena Berita, Antoinette Alarja, Natalie A. Xiu, Leshan Merchant, James A. Binder, Raquel A. Goh, Johnny Keh-Tun Guernier-Cambert, Vanina Galán, Diego Gregory, Michael J. Gray, Gregory C. Leptospirosis infections among hospital patients, Sarawak, Malaysia |
title | Leptospirosis infections among hospital patients, Sarawak, Malaysia |
title_full | Leptospirosis infections among hospital patients, Sarawak, Malaysia |
title_fullStr | Leptospirosis infections among hospital patients, Sarawak, Malaysia |
title_full_unstemmed | Leptospirosis infections among hospital patients, Sarawak, Malaysia |
title_short | Leptospirosis infections among hospital patients, Sarawak, Malaysia |
title_sort | leptospirosis infections among hospital patients, sarawak, malaysia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559352/ https://www.ncbi.nlm.nih.gov/pubmed/34719397 http://dx.doi.org/10.1186/s40794-021-00154-2 |
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