Antigen-based diagnosis of Schistosoma infection in travellers: a prospective study.


Journal

Journal of travel medicine
ISSN: 1708-8305
Titre abrégé: J Travel Med
Pays: England
ID NLM: 9434456

Informations de publication

Date de publication:
14 Jul 2020
Historique:
received: 02 03 2020
revised: 09 04 2020
accepted: 10 04 2020
pubmed: 21 4 2020
medline: 17 6 2021
entrez: 21 4 2020
Statut: ppublish

Résumé

Travellers infected with Schistosoma spp. might be pauci- or even asymptomatic on first presentation. Therefore, schistosomiasis may remain undiagnosed in this population. Active infection, as evidenced by the presence of the tissue-dwelling worm, can be demonstrated via the detection of adult worm-derived circulating anodic antigen (CAA) utilising a robust well-described lateral flow-(LF) based test applying background-free up-converting reporter particles (UCP). In this prospective study, we assessed the diagnostic value of serum and urine UCP-LF CAA test in comparison with two Schistosoma-specific serological assays detecting antibodies against adult worm antigen-immuno fluorescence assay (AWA-IFA) and against soluble egg antigen-enzyme-linked immunosorbent assay (SEA-ELISA) antigens in travellers. Samples were collected from 106 Dutch travellers who reported freshwater contact in sub-Saharan Africa and who were recruited up to 2 years after return. Subjects were asked to complete a detailed questionnaire on travel history, water contact, signs and symptoms compatible with schistosomiasis. Two travellers were positive by serum CAA and an additional one by urine CAA. A total of 22/106 (21%) samples were antibody positive by AWA-IFA and 9/106 (9%) by SEA-ELISA. At follow-up 6 weeks and 6 months after praziquantel treatment, all seropositives remained antibody positive whereas CAA was cleared. Seropositivity could not be predicted by the type of fresh water-related activity, country visited or symptoms reported. The low number of UCP-LF CAA positives suggests that in travellers, active infections often do not establish or have very low worm burden. Based on our high seroconversion rates, we conclude that the AWA-IFA assay is the most sensitive test to detect schistosome exposure. Given the lack of predictive symptoms or risk factors, we recommend schistosomiasis screening at least by serology in all travellers with reported freshwater contact in high-endemic areas.

Sections du résumé

BACKGROUND BACKGROUND
Travellers infected with Schistosoma spp. might be pauci- or even asymptomatic on first presentation. Therefore, schistosomiasis may remain undiagnosed in this population. Active infection, as evidenced by the presence of the tissue-dwelling worm, can be demonstrated via the detection of adult worm-derived circulating anodic antigen (CAA) utilising a robust well-described lateral flow-(LF) based test applying background-free up-converting reporter particles (UCP). In this prospective study, we assessed the diagnostic value of serum and urine UCP-LF CAA test in comparison with two Schistosoma-specific serological assays detecting antibodies against adult worm antigen-immuno fluorescence assay (AWA-IFA) and against soluble egg antigen-enzyme-linked immunosorbent assay (SEA-ELISA) antigens in travellers.
METHODS METHODS
Samples were collected from 106 Dutch travellers who reported freshwater contact in sub-Saharan Africa and who were recruited up to 2 years after return. Subjects were asked to complete a detailed questionnaire on travel history, water contact, signs and symptoms compatible with schistosomiasis.
RESULTS RESULTS
Two travellers were positive by serum CAA and an additional one by urine CAA. A total of 22/106 (21%) samples were antibody positive by AWA-IFA and 9/106 (9%) by SEA-ELISA. At follow-up 6 weeks and 6 months after praziquantel treatment, all seropositives remained antibody positive whereas CAA was cleared. Seropositivity could not be predicted by the type of fresh water-related activity, country visited or symptoms reported.
CONCLUSION CONCLUSIONS
The low number of UCP-LF CAA positives suggests that in travellers, active infections often do not establish or have very low worm burden. Based on our high seroconversion rates, we conclude that the AWA-IFA assay is the most sensitive test to detect schistosome exposure. Given the lack of predictive symptoms or risk factors, we recommend schistosomiasis screening at least by serology in all travellers with reported freshwater contact in high-endemic areas.

Identifiants

pubmed: 32307517
pii: 5822102
doi: 10.1093/jtm/taaa055
pmc: PMC7359925
pii:
doi:

Substances chimiques

Antibodies, Helminth 0
Antigens, Helminth 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© International Society of Travel Medicine 2020.

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Auteurs

Miriam Casacuberta-Partal (M)

Department of Parasitology, Leiden University Medical Centre, L4-Q, PO Box 9600, 2333 ZA Leiden, The Netherlands.

Jacqueline J Janse (JJ)

Department of Parasitology, Leiden University Medical Centre, L4-Q, PO Box 9600, 2333 ZA Leiden, The Netherlands.

Roos van Schuijlenburg (R)

Department of Parasitology, Leiden University Medical Centre, L4-Q, PO Box 9600, 2333 ZA Leiden, The Netherlands.

Jutte J C de Vries (JJC)

Department of Medical Microbiology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Marianne A A Erkens (MAA)

Department of Medical Microbiology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Kitty Suijk (K)

Department of Infectious Diseases, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Mariëlle van Aalst (M)

Centre of Tropical Medicine and Travel Medicine, Amsterdam University Medical Centres, AMC, University of Amsterdam, 1100 DD Amsterdam, The Netherlands.

Jaap J Maas (JJ)

Occupational Health and Safety Service, Amsterdam University Medical Centres, AMC, University of Amsterdam, 1100 DD Amsterdam, The Netherlands.

Martin P Grobusch (MP)

Centre of Tropical Medicine and Travel Medicine, Amsterdam University Medical Centres, AMC, University of Amsterdam, 1100 DD Amsterdam, The Netherlands.

Perry J J van Genderen (PJJ)

Institute for Tropical Diseases, Erasmus University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.

Claudia de Dood (C)

Department of Cell and Chemical Biology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Paul L A M Corstjens (PLAM)

Department of Cell and Chemical Biology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Govert J van Dam (GJ)

Department of Parasitology, Leiden University Medical Centre, L4-Q, PO Box 9600, 2333 ZA Leiden, The Netherlands.

Lisette van Lieshout (L)

Department of Parasitology, Leiden University Medical Centre, L4-Q, PO Box 9600, 2333 ZA Leiden, The Netherlands.
Department of Medical Microbiology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Meta Roestenberg (M)

Department of Parasitology, Leiden University Medical Centre, L4-Q, PO Box 9600, 2333 ZA Leiden, The Netherlands.
Department of Infectious Diseases, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

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Classifications MeSH