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Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study

Scrub typhus (ST) is a neglected acute, febrile, infectious disease caused by the intracellular parasite Orientia tsutsugamushi, a gram-negative coccobacillus of the family Rickettsiaceae. Early and precise diagnosis is crucial to reduce the risk of developing disease complications. However, IgM ant...

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Autores principales: Seetha, Dayakar, Nori, Sai Ravi Chandra, Nair, Radhakrishnan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889949/
https://www.ncbi.nlm.nih.gov/pubmed/36741550
http://dx.doi.org/10.1007/s00580-023-03443-8
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author Seetha, Dayakar
Nori, Sai Ravi Chandra
Nair, Radhakrishnan R.
author_facet Seetha, Dayakar
Nori, Sai Ravi Chandra
Nair, Radhakrishnan R.
author_sort Seetha, Dayakar
collection PubMed
description Scrub typhus (ST) is a neglected acute, febrile, infectious disease caused by the intracellular parasite Orientia tsutsugamushi, a gram-negative coccobacillus of the family Rickettsiaceae. Early and precise diagnosis is crucial to reduce the risk of developing disease complications. However, IgM antibody enzyme-linked immunosorbent assay (IgM ELISA) and indirect immunofluorescence assay (IFA) remain essential for diagnosis. However, it could be more helpful for early diagnosis due to the need for uniformity of approach in the diagnostic accuracy studies to determine appropriate ELISA cut-offs for various geographic locations. Hence, we aim to study the O. tsutsugamushi type-specific 56 kilodalton (kDa) protein gene using nested PCR (nPCR) and DNA sequence analysis as a molecular marker for early diagnosis. Out of 10,439 suspected cases, 1147/10,439 (11%) patients were positive for IgM ELISA. A total of 1044/10,439 (10%) samples were randomly tested after nPCR and compared with IgM ELISA results and DNA sequence analysis. Using nested PCR and IgM ELISA methods, 13% (134/1044) and 12% (125/1044) of the samples were positive, respectively. The serology method could not replicate the substantial number of positive cases demonstrated by nPCR; therefore, significant mutual exclusivity of the two techniques requires further investigation. Furthermore, our phylogenetic analysis revealed a clustering of isolates with Karp-related strains, providing insight into the transmission dynamics. Therefore, molecular diagnostic methods may aid in the early diagnosis of infection and enable prompt treatment of ST in endemic regions. Our results show that IgM ELISA can provide complete diagnostic advantages in conjunction with nPCR and can be an essential tool for accurate diagnosis. In addition, the DNA sequencing analysis of the samples showed that Karp-related strains were the main strains. Furthermore, research with samples from various regions in combination with the entire genome sequencing of O. tsutsugamushi is required to understand the infection mechanism better and develop robust early detection methods. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00580-023-03443-8.
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spelling pubmed-98899492023-02-01 Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study Seetha, Dayakar Nori, Sai Ravi Chandra Nair, Radhakrishnan R. Comp Clin Path Original Article Scrub typhus (ST) is a neglected acute, febrile, infectious disease caused by the intracellular parasite Orientia tsutsugamushi, a gram-negative coccobacillus of the family Rickettsiaceae. Early and precise diagnosis is crucial to reduce the risk of developing disease complications. However, IgM antibody enzyme-linked immunosorbent assay (IgM ELISA) and indirect immunofluorescence assay (IFA) remain essential for diagnosis. However, it could be more helpful for early diagnosis due to the need for uniformity of approach in the diagnostic accuracy studies to determine appropriate ELISA cut-offs for various geographic locations. Hence, we aim to study the O. tsutsugamushi type-specific 56 kilodalton (kDa) protein gene using nested PCR (nPCR) and DNA sequence analysis as a molecular marker for early diagnosis. Out of 10,439 suspected cases, 1147/10,439 (11%) patients were positive for IgM ELISA. A total of 1044/10,439 (10%) samples were randomly tested after nPCR and compared with IgM ELISA results and DNA sequence analysis. Using nested PCR and IgM ELISA methods, 13% (134/1044) and 12% (125/1044) of the samples were positive, respectively. The serology method could not replicate the substantial number of positive cases demonstrated by nPCR; therefore, significant mutual exclusivity of the two techniques requires further investigation. Furthermore, our phylogenetic analysis revealed a clustering of isolates with Karp-related strains, providing insight into the transmission dynamics. Therefore, molecular diagnostic methods may aid in the early diagnosis of infection and enable prompt treatment of ST in endemic regions. Our results show that IgM ELISA can provide complete diagnostic advantages in conjunction with nPCR and can be an essential tool for accurate diagnosis. In addition, the DNA sequencing analysis of the samples showed that Karp-related strains were the main strains. Furthermore, research with samples from various regions in combination with the entire genome sequencing of O. tsutsugamushi is required to understand the infection mechanism better and develop robust early detection methods. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00580-023-03443-8. Springer London 2023-02-01 2023 /pmc/articles/PMC9889949/ /pubmed/36741550 http://dx.doi.org/10.1007/s00580-023-03443-8 Text en © The Author(s), under exclusive licence to Springer-Verlag London Ltd., part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Seetha, Dayakar
Nori, Sai Ravi Chandra
Nair, Radhakrishnan R.
Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study
title Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study
title_full Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study
title_fullStr Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study
title_full_unstemmed Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study
title_short Molecular-based study of scrub typhus in Kerala, South India from 2014 to 2021: a laboratory-based study
title_sort molecular-based study of scrub typhus in kerala, south india from 2014 to 2021: a laboratory-based study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889949/
https://www.ncbi.nlm.nih.gov/pubmed/36741550
http://dx.doi.org/10.1007/s00580-023-03443-8
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