Comparison of the Serion IgM ELISA and Microscopic Agglutination Test for diagnosis of Leptospira spp. infections in sera from different geographical origins and estimation of Leptospira seroprevalence in the Wiwa indigenous population from Colombia.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
06 2022
Historique:
received: 06 10 2021
accepted: 22 04 2022
revised: 23 06 2022
pubmed: 7 6 2022
medline: 28 6 2022
entrez: 6 6 2022
Statut: epublish

Résumé

Leptospirosis is among the most important zoonotic diseases in (sub-)tropical countries. The research objective was to evaluate the accuracy of the Serion IgM ELISA EST125M against the Microscopic Agglutination Test (MAT = imperfect reference test); to assess its ability to diagnose acute leptospirosis infections and to detect previous exposure to leptospires in an endemic setting. In addition, to estimate the overall Leptospira spp. seroprevalence in the Wiwa indigenous population in North-East Colombia. We analysed serum samples from confirmed leptospirosis patients from the Netherlands (N = 14), blood donor sera from Switzerland (N = 20), and sera from a cross-sectional study in Colombia (N = 321). All leptospirosis ELISA-positive, and a random of negative samples from Colombia were tested by the MAT for confirmation. The ELISA performed with a sensitivity of 100% (95% CI 77% - 100%) and a specificity of 100% (95% CI 83% - 100%) based on MAT confirmed Leptospira spp. positive and negative samples. In the cross-sectional study in Colombia, the ELISA performed with a sensitivity of 100% (95% CI 2-100%) and a specificity of 21% (95% CI 15-28%). Assuming a 5% Leptospira spp. seroprevalence in this population, the positive predictive value was 6% and the negative predictive value 100%. The Leptospira spp. seroprevalence in the Wiwas tested by the ELISA was 39%; however, by MAT only 0.3%. The ELISA is suitable to diagnose leptospirosis in acutely ill patients in Europe several days after onset of disease. For cross-sectional studies it is not recommended due to its low specificity. Despite the evidence of a high leptospirosis prevalence in other study areas and populations in Colombia, the Wiwa do not seem to be highly exposed to Leptospira spp.. Nevertheless, leptospirosis should be considered and tested in patients presenting with febrile illness.

Identifiants

pubmed: 35666764
doi: 10.1371/journal.pntd.0009876
pii: PNTD-D-21-01462
pmc: PMC9223614
doi:

Substances chimiques

Antibodies, Bacterial 0
Immunoglobulin M 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0009876

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Anou Dreyfus (A)

Department of Medicine, Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.
Epidemiology and Clinical Research Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.

Marie-Thérèse Ruf (MT)

Department of Medicine, Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.

Marga Goris (M)

Department of Medical Microbiology and Infection Prevention, OIE and National Collaborating Centre for Reference and Research on Leptospirosis, Amsterdam University Medical Centre, Amsterdam, the Netherlands.

Sven Poppert (S)

Department of Medicine, Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.

Anne Mayer-Scholl (A)

Department of Biological Safety, German Federal Institute for Risk Assessment, Berlin, Germany.

Nadine Loosli (N)

Department of Medicine, Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.

Nadja S Bier (NS)

Department of Biological Safety, German Federal Institute for Risk Assessment, Berlin, Germany.

Daniel H Paris (DH)

Department of Medicine, Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.

Tshokey Tshokey (T)

Department of Pathology and Laboratory Medicine, Jigme Dorji Wangchuck National Referral Hospital, Thimphu, Bhutan.
Faculty of Postgraduate Medicine, Khesar Gyalpo University of Medical Sciences of Bhutan, Thimphu, Bhutan.

John Stenos (J)

Australian Rickettsial Reference Laboratory, University Hospital Geelong, Geelong, Australia.

Eliharintsoa Rajaonarimirana (E)

Epidemiology and Clinical Research Unit, Institut Pasteur de Madagascar, Antananarivo, Madagascar.

Gustavo Concha (G)

Organización Wiwa Yugumaiun Bunkuanarua Tairona (OWBYT) Valledupar, Colombia.

Jorge Orozco (J)

La Secretaría de Salud Departamental de la Gobernación de Cesar, Valledupar, Colombia.

Johana Colorado (J)

Laboratorio de Salud Pública de la Secretaría de Salud Departamental, Valledupar, Colombia.

Andrés Aristizábal (A)

Fundación Salud Para El Trópico (FSPT), Santa Marta, Colombia.

Juan C Dib (JC)

Fundación Salud Para El Trópico (FSPT), Santa Marta, Colombia.
Department of Medicine, Fundación Universidad del Norte, Barranquilla, Colombia.

Simone Kann (S)

Medical Mission Institute, Wuerzburg, Germany.

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Classifications MeSH