Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice

Trypanosoma brucei gambiense (T. b. gambiense) is the major causative agent of human African trypanosomiasis (HAT). A great variety of clinical outcomes have been observed in West African foci, probably due to complex host-parasite interactions. In order to separate the roles of parasite genetic diversity and host variability, we have chosen to precisely characterize the pathogenicity and virulence of T. b. gambiense field isolates in a mouse model. Thirteen T. b. gambiense strains were studied in experimental infections, with 20 Balb/C infected mice per isolate. Mice were monitored for 30 days, in which mortality, parasitemia, anemia, and weight were recorded. Mortality rate, prepatent period, and maximum parasitemia were estimated, and a survival analysis was performed to compare strain pathogenicity. Mixed models were used to assess parasitemia dynamics, weight, and changes in Packed Cell Volume (PCV). Finally, a multivariate analysis was performed to infer relationships between all variables. A large phenotypic diversity was observed. Pathogenicity was highly variable, ranging from strains that kill their host within 9 days to a non-pathogenic strain (no deaths during the experiment). Virulence was also variable, with maximum parasitemia values ranging from 42 million to 1 billion trypanosomes/ml. Reduced PCV and weight occurred in the first two weeks of the infection, with the exception of two strains. Finally, the global analysis highlighted three groups of strains: a first group with highly pathogenic strains showing an early mortality associated with a short prepatent period; a second group of highly virulent strains with intermediate pathogenicity; and a third group of isolates characterized by low pathogenicity and virulence patterns. Such biological differences could be related to the observed clinical diversity in HAT. A better understanding of the biological pathways underlying the observed phenotypic diversity could thus help to clarify the complex nature of the host-parasite interactions that determine the resistance/susceptibility status to T. brucei gambiense.

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Main Authors: Kaboré, Jacques, Camara, Oumou, Koffi, Mathurin, Sanou, Djénéba, Ilboudou, Hamidou, Sakande, Hassane, Camara, Mamadou, De Meeus, Thierry, Ravel, Sophie, Belem, Adrien Marie Gaston, MacLeod, Annette, Bucheton, Bruno, Jamonneau, Vincent, Thevenon, Sophie
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Language:eng
Subjects:L72 - Organismes nuisibles des animaux, 000 - Autres thèmes, http://aims.fao.org/aos/agrovoc/c_4027, http://aims.fao.org/aos/agrovoc/c_3423,
Online Access:http://agritrop.cirad.fr/588093/
http://agritrop.cirad.fr/588093/1/Kabore%20et%20al%202018.pdf
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spelling dig-cirad-fr-5880932022-09-09T06:12:43Z http://agritrop.cirad.fr/588093/ http://agritrop.cirad.fr/588093/ Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice. Kaboré Jacques, Camara Oumou, Koffi Mathurin, Sanou Djénéba, Ilboudou Hamidou, Sakande Hassane, Camara Mamadou, De Meeus Thierry, Ravel Sophie, Belem Adrien Marie Gaston, MacLeod Annette, Bucheton Bruno, Jamonneau Vincent, Thevenon Sophie. 2018. Infection, Genetics and Evolution, 63 : 269-276.https://doi.org/10.1016/j.meegid.2018.05.018 <https://doi.org/10.1016/j.meegid.2018.05.018> Researchers Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice Kaboré, Jacques Camara, Oumou Koffi, Mathurin Sanou, Djénéba Ilboudou, Hamidou Sakande, Hassane Camara, Mamadou De Meeus, Thierry Ravel, Sophie Belem, Adrien Marie Gaston MacLeod, Annette Bucheton, Bruno Jamonneau, Vincent Thevenon, Sophie eng 2018 Infection, Genetics and Evolution L72 - Organismes nuisibles des animaux 000 - Autres thèmes Côte d'Ivoire Guinée http://aims.fao.org/aos/agrovoc/c_4027 http://aims.fao.org/aos/agrovoc/c_3423 Trypanosoma brucei gambiense (T. b. gambiense) is the major causative agent of human African trypanosomiasis (HAT). A great variety of clinical outcomes have been observed in West African foci, probably due to complex host-parasite interactions. In order to separate the roles of parasite genetic diversity and host variability, we have chosen to precisely characterize the pathogenicity and virulence of T. b. gambiense field isolates in a mouse model. Thirteen T. b. gambiense strains were studied in experimental infections, with 20 Balb/C infected mice per isolate. Mice were monitored for 30 days, in which mortality, parasitemia, anemia, and weight were recorded. Mortality rate, prepatent period, and maximum parasitemia were estimated, and a survival analysis was performed to compare strain pathogenicity. Mixed models were used to assess parasitemia dynamics, weight, and changes in Packed Cell Volume (PCV). Finally, a multivariate analysis was performed to infer relationships between all variables. A large phenotypic diversity was observed. Pathogenicity was highly variable, ranging from strains that kill their host within 9 days to a non-pathogenic strain (no deaths during the experiment). Virulence was also variable, with maximum parasitemia values ranging from 42 million to 1 billion trypanosomes/ml. Reduced PCV and weight occurred in the first two weeks of the infection, with the exception of two strains. Finally, the global analysis highlighted three groups of strains: a first group with highly pathogenic strains showing an early mortality associated with a short prepatent period; a second group of highly virulent strains with intermediate pathogenicity; and a third group of isolates characterized by low pathogenicity and virulence patterns. Such biological differences could be related to the observed clinical diversity in HAT. A better understanding of the biological pathways underlying the observed phenotypic diversity could thus help to clarify the complex nature of the host-parasite interactions that determine the resistance/susceptibility status to T. brucei gambiense. article info:eu-repo/semantics/article Journal Article info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/588093/1/Kabore%20et%20al%202018.pdf text Cirad license info:eu-repo/semantics/restrictedAccess https://agritrop.cirad.fr/mention_legale.html https://doi.org/10.1016/j.meegid.2018.05.018 10.1016/j.meegid.2018.05.018 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.meegid.2018.05.018 info:eu-repo/semantics/altIdentifier/purl/https://doi.org/10.1016/j.meegid.2018.05.018
institution CIRAD FR
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-cirad-fr
tag biblioteca
region Europa del Oeste
libraryname Biblioteca del CIRAD Francia
language eng
topic L72 - Organismes nuisibles des animaux
000 - Autres thèmes
http://aims.fao.org/aos/agrovoc/c_4027
http://aims.fao.org/aos/agrovoc/c_3423
L72 - Organismes nuisibles des animaux
000 - Autres thèmes
http://aims.fao.org/aos/agrovoc/c_4027
http://aims.fao.org/aos/agrovoc/c_3423
spellingShingle L72 - Organismes nuisibles des animaux
000 - Autres thèmes
http://aims.fao.org/aos/agrovoc/c_4027
http://aims.fao.org/aos/agrovoc/c_3423
L72 - Organismes nuisibles des animaux
000 - Autres thèmes
http://aims.fao.org/aos/agrovoc/c_4027
http://aims.fao.org/aos/agrovoc/c_3423
Kaboré, Jacques
Camara, Oumou
Koffi, Mathurin
Sanou, Djénéba
Ilboudou, Hamidou
Sakande, Hassane
Camara, Mamadou
De Meeus, Thierry
Ravel, Sophie
Belem, Adrien Marie Gaston
MacLeod, Annette
Bucheton, Bruno
Jamonneau, Vincent
Thevenon, Sophie
Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice
description Trypanosoma brucei gambiense (T. b. gambiense) is the major causative agent of human African trypanosomiasis (HAT). A great variety of clinical outcomes have been observed in West African foci, probably due to complex host-parasite interactions. In order to separate the roles of parasite genetic diversity and host variability, we have chosen to precisely characterize the pathogenicity and virulence of T. b. gambiense field isolates in a mouse model. Thirteen T. b. gambiense strains were studied in experimental infections, with 20 Balb/C infected mice per isolate. Mice were monitored for 30 days, in which mortality, parasitemia, anemia, and weight were recorded. Mortality rate, prepatent period, and maximum parasitemia were estimated, and a survival analysis was performed to compare strain pathogenicity. Mixed models were used to assess parasitemia dynamics, weight, and changes in Packed Cell Volume (PCV). Finally, a multivariate analysis was performed to infer relationships between all variables. A large phenotypic diversity was observed. Pathogenicity was highly variable, ranging from strains that kill their host within 9 days to a non-pathogenic strain (no deaths during the experiment). Virulence was also variable, with maximum parasitemia values ranging from 42 million to 1 billion trypanosomes/ml. Reduced PCV and weight occurred in the first two weeks of the infection, with the exception of two strains. Finally, the global analysis highlighted three groups of strains: a first group with highly pathogenic strains showing an early mortality associated with a short prepatent period; a second group of highly virulent strains with intermediate pathogenicity; and a third group of isolates characterized by low pathogenicity and virulence patterns. Such biological differences could be related to the observed clinical diversity in HAT. A better understanding of the biological pathways underlying the observed phenotypic diversity could thus help to clarify the complex nature of the host-parasite interactions that determine the resistance/susceptibility status to T. brucei gambiense.
format article
topic_facet L72 - Organismes nuisibles des animaux
000 - Autres thèmes
http://aims.fao.org/aos/agrovoc/c_4027
http://aims.fao.org/aos/agrovoc/c_3423
author Kaboré, Jacques
Camara, Oumou
Koffi, Mathurin
Sanou, Djénéba
Ilboudou, Hamidou
Sakande, Hassane
Camara, Mamadou
De Meeus, Thierry
Ravel, Sophie
Belem, Adrien Marie Gaston
MacLeod, Annette
Bucheton, Bruno
Jamonneau, Vincent
Thevenon, Sophie
author_facet Kaboré, Jacques
Camara, Oumou
Koffi, Mathurin
Sanou, Djénéba
Ilboudou, Hamidou
Sakande, Hassane
Camara, Mamadou
De Meeus, Thierry
Ravel, Sophie
Belem, Adrien Marie Gaston
MacLeod, Annette
Bucheton, Bruno
Jamonneau, Vincent
Thevenon, Sophie
author_sort Kaboré, Jacques
title Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice
title_short Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice
title_full Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice
title_fullStr Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice
title_full_unstemmed Differences in pathogenicity and virulence of Trypanosoma brucei gambiense field isolates in experimentally infected Balb/C mice
title_sort differences in pathogenicity and virulence of trypanosoma brucei gambiense field isolates in experimentally infected balb/c mice
url http://agritrop.cirad.fr/588093/
http://agritrop.cirad.fr/588093/1/Kabore%20et%20al%202018.pdf
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