TY - JOUR
T1 - Leptospirosis infections among hospital patients, Sarawak, Malaysia
AU - Hii, King Ching
AU - Robie, Emily R.
AU - Saihidi, Izreena
AU - Berita, Antoinette
AU - Alarja, Natalie A.
AU - Xiu, Leshan
AU - Merchant, James A.
AU - Binder, Raquel A.
AU - Goh, Johnny Keh Tun
AU - Guernier-Cambert, Vanina
AU - Galán, Diego
AU - Gregory, Michael J.
AU - Gray, Gregory C.
N1 - Funding Information:
We thank the Director General of Health Malaysia for his permission to publish this article. This work was conducted in partnership with Duke University, the Duke Global Health Institute, Sibu Hospital Clinical Research Center, SEGi University Sibu Clinical Campus, and the Ministry of Health Malaysia. This study was supported by Vysnova and Naval Medical Research Unit 2. Special thanks to Lee Nung Kion from Faculty of Cognitive Sciences and Human Development, University Malaysia Sarawak for contributing statistical analyses. Special thanks, also, to Jakie Ting and Tiing-Tiing Chua for collaboration in handling specimens between Sibu, Sarikei and Kapit Hospital. We appreciate Ivan Jan-Shui Vun, Huong-Nai Law, Khiu Fu Lung, Pravind Narayanan, Ing-Tien Wong, Toh-Mee Wong for supervising at the respective study sites. We thank the medical officers Jia-Yun Chuang, Wei-Yieng Tang, Fong-Kean Lim, Shen-Ly Lai, Syn-Hwan Wong, Awang Emir Naim, Eng-Seng Tiew, Chiong-Kim Law, Jeffrey Soon-Yit, Lee, Jun-Wei Liew, Rashmika Nambiar, Edmund Kwong-Yuen Wong, Bing-En Chia for recruiting study participants at Kapit, Sarikei, and Sibu Hospitals. We thank laboratory technicians Hieng-Hua Goh of Kapit Hospital and the laboratory technicians from Sibu and Sarikei for preparing clinical specimens for study. We also appreciate the drivers and those who helped with transporting specimens.
Funding Information:
We thank the Director General of Health Malaysia for his permission to publish this article. This work was conducted in partnership with Duke University, the Duke Global Health Institute, Sibu Hospital Clinical Research Center, SEGi University Sibu Clinical Campus, and the Ministry of Health Malaysia. This study was supported by Vysnova and Naval Medical Research Unit 2. Special thanks to Lee Nung Kion from Faculty of Cognitive Sciences and Human Development, University Malaysia Sarawak for contributing statistical analyses. Special thanks, also, to Jakie Ting and Tiing-Tiing Chua for collaboration in handling specimens between Sibu, Sarikei and Kapit Hospital. We appreciate Ivan Jan-Shui Vun, Huong-Nai Law, Khiu Fu Lung, Pravind Narayanan, Ing-Tien Wong, Toh-Mee Wong for supervising at the respective study sites. We thank the medical officers Jia-Yun Chuang, Wei-Yieng Tang, Fong-Kean Lim, Shen-Ly Lai, Syn-Hwan Wong, Awang Emir Naim, Eng-Seng Tiew, Chiong-Kim Law, Jeffrey Soon-Yit, Lee, Jun-Wei Liew, Rashmika Nambiar, Edmund Kwong-Yuen Wong, Bing-En Chia for recruiting study participants at Kapit, Sarikei, and Sibu Hospitals. We thank laboratory technicians Hieng-Hua Goh of Kapit Hospital and the laboratory technicians from Sibu and Sarikei for preparing clinical specimens for study. We also appreciate the drivers and those who helped with transporting specimens.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - 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.
AB - 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.
KW - Diagnostics
KW - Leptospirosis
KW - Malaysia
KW - Sarawak
UR - http://www.scopus.com/inward/record.url?scp=85118332139&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85118332139&partnerID=8YFLogxK
U2 - 10.1186/s40794-021-00154-2
DO - 10.1186/s40794-021-00154-2
M3 - Article
AN - SCOPUS:85118332139
SN - 2055-0936
VL - 7
JO - Tropical Diseases, Travel Medicine and Vaccines
JF - Tropical Diseases, Travel Medicine and Vaccines
IS - 1
M1 - 32
ER -