Extravascular Dermal Trypanosomes in Suspected and Confirmed Cases of gambiense Human African Trypanosomiasis

Author:

Camara Mariame1,Soumah Alseny M’mah12,Ilboudo Hamidou134,Travaillé Christelle5,Clucas Caroline6,Cooper Anneli6,Kuispond Swar Nono-Raymond67,Camara Oumou1,Sadissou Ibrahim4,Calvo Alvarez Estefania5,Crouzols Aline5,Bart Jean-Mathieu4,Jamonneau Vincent4,Camara Mamadou1,MacLeod Annette6,Bucheton Bruno14,Rotureau Brice5ORCID

Affiliation:

1. Programme National de Lutte Contre la Trypanosomiase Humaine Africaine, Ministère de la Santé, Conakry, Guinea

2. Service de Dermatologie, Hôpital de Donka,Conakry, Guinea

3. Institut de Recherche en Sciences de la Santé (IRSS)—Unité de Recherche Clinique de Nanoro (URCN), Nanoro, Burkina-Faso

4. Institut de Recherche pour le Développement, Unité Mixte de Recherche Institut de Recherche pour le Développement (IRD)-CIRAD 177 InterTryp, Campus International de Baillarguet, Montpellier, France

5. Trypanosome Transmission Group, Trypanosome Cell Biology Unit, Institut National de la Santé et de la Recherche Médicale (INSERM) U1201 and Department of Parasites and Insect Vectors, Institut Pasteur, Paris, France

6. Wellcome Centre for Integrative Parasitology, College of Medical, Veterinary, and Life Sciences, Henry Wellcome Building for Comparative Medical Sciences, Glasgow, Scotland, United Kingdom

7. Department of Parasitology, National Institute of Biomedical Research (INRB), Kinshasa, Democratic Republic of the Congo

Abstract

Abstract Background The diagnosis of gambiense human African trypanosomiasis (gHAT) typically involves 2 steps: a serological screen, followed by the detection of living trypanosome parasites in the blood or lymph node aspirate. Live parasites can, however, remain undetected in some seropositive individuals, who, we hypothesize, are infected with Trypanosoma brucei gambiense parasites in their extravascular dermis. Methods To test this hypothesis, we conducted a prospective observational cohort study in the gHAT focus of Forecariah, Republic of Guinea. Of the 5417 subjects serologically screened for gHAT, 66 were enrolled into our study and underwent a dermatological examination. At enrollment, 11 seronegative, 8 unconfirmed seropositive, and 18 confirmed seropositive individuals had blood samples and skin biopsies taken and examined for trypanosomes by molecular and immunohistological methods. Results In seropositive individuals, dermatological symptoms were significantly more frequent, relative to seronegative controls. T.b. gambiense parasites were present in the blood of all confirmed cases (n = 18) but not in unconfirmed seropositive individuals (n = 8). However, T. brucei parasites were detected in the extravascular dermis of all unconfirmed seropositive individuals and all confirmed cases. Skin biopsies of all treated cases and most seropositive untreated individuals progressively became negative for trypanosomes 6 and 20 months later. Conclusions Our results highlight the skin as a potential reservoir for African trypanosomes, with implications for our understanding of this disease’s epidemiology in the context of its planned elimination and underlining the skin as a novel target for gHAT diagnostics.

Funder

Wellcome Trust

Institut de Recherche pour le Développement

French National Agency for Scientific Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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