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The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice

There is burgeoning interest in the complex tripartite interplays between the commensal microbiota, host's genetic factors, and immune response during helminth infections which are still poorly understood. The study explores this relationship in the context of chronic schistosomiasis-driven patholog...

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Main Author: Mpotje, Thabo Rantanta Victor
Other Authors: Brombacher, F
Format: Thesis
Language:English
Published: Department of Pathology 2021
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access_status_str Open Access
author Mpotje, Thabo Rantanta Victor
author2 Brombacher, F
author_browse Brombacher, F
Mpotje, Thabo Rantanta Victor
author_facet Brombacher, F
Mpotje, Thabo Rantanta Victor
author_sort Mpotje, Thabo Rantanta Victor
collection Thesis
description There is burgeoning interest in the complex tripartite interplays between the commensal microbiota, host's genetic factors, and immune response during helminth infections which are still poorly understood. The study explores this relationship in the context of chronic schistosomiasis-driven pathology. In the first part of the thesis, removal of the host Basic Leucine Zipper ATF-Like Transcription Factor 2 (Batf2) gene in 129Sv (Batf2-/- ) mice resulted in alteration of the intestinal microbial composition and reduced granulomatous inflammatory immune response. These changes associated with rescue from pre-mature mortality and improved fitness of Batf2-/- mice during chronic experimental schistosomiasis in relation to control wild type mice. The prolonged survival and reduced immunopathology were diminished by treatment with α-CD8 antibody highlighting the significance of CD8-expressing immune mediators during chronic Schistosomiasis. Transfer of the altered intestinal microbiota from Batf2-/- mice to wild type mice by co-housing was enough to rescue the latter from exacerbated granulomatous inflammation and prolonged their survival during chronic schistosomiasis. These observations suggest, for the first time, a central role of the host gut microbiota in decisively regulating the tissue immune response, the elicited pathology and host survival during schistosomiasis. To validate the robustness of this tripartite interaction during chronic schistosomiasis around the gut microbiota, the second part of the present work analysed two genetically identical murine models (C57BL/6) housed under two different specific Pathogen free environments (SPF1 and SPF2) and presenting differential susceptibility to chronic schistosomiasis. Our work revealed a higher susceptibility of C57BL/6 mice from the SPF2 facility in relation to C57BL/6 mice from the SPF1 facility. In confirmation with our first series of experiments, that demonstrated a central role of the host intestinal microbiota in regulating the immune responses, the pathology, and the survival of the host during schistosomiasis, the second series of experiments further presented an ameliorated immunological, pathological and vital prognosis of vulnerable SPF2 C57BL/6 mice receiving the intestinal microbiota of more resistant SPF1 C57BL/6 mice. Therefore, the study demonstrates the genetic regulation of gut microbiota which in turn, and/or in concert with the genetic make-up, influence the immunological, pathological, and vital host response during chronic schistosomiasis. The present work expands the conventional knowledge on schistosomiasis disease regulation and presents the gene-microbiota-immune-response interactome as a core piece of the regulatory machinery of this infection as exploitable to alter disease progression in the context of drug and vaccine development.
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institution University of Cape Town (South Africa)
language eng
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license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2021
publishDateRange 2021
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/33888 The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice Mpotje, Thabo Rantanta Victor Brombacher, F Gray, Clive Pathology There is burgeoning interest in the complex tripartite interplays between the commensal microbiota, host's genetic factors, and immune response during helminth infections which are still poorly understood. The study explores this relationship in the context of chronic schistosomiasis-driven pathology. In the first part of the thesis, removal of the host Basic Leucine Zipper ATF-Like Transcription Factor 2 (Batf2) gene in 129Sv (Batf2-/- ) mice resulted in alteration of the intestinal microbial composition and reduced granulomatous inflammatory immune response. These changes associated with rescue from pre-mature mortality and improved fitness of Batf2-/- mice during chronic experimental schistosomiasis in relation to control wild type mice. The prolonged survival and reduced immunopathology were diminished by treatment with α-CD8 antibody highlighting the significance of CD8-expressing immune mediators during chronic Schistosomiasis. Transfer of the altered intestinal microbiota from Batf2-/- mice to wild type mice by co-housing was enough to rescue the latter from exacerbated granulomatous inflammation and prolonged their survival during chronic schistosomiasis. These observations suggest, for the first time, a central role of the host gut microbiota in decisively regulating the tissue immune response, the elicited pathology and host survival during schistosomiasis. To validate the robustness of this tripartite interaction during chronic schistosomiasis around the gut microbiota, the second part of the present work analysed two genetically identical murine models (C57BL/6) housed under two different specific Pathogen free environments (SPF1 and SPF2) and presenting differential susceptibility to chronic schistosomiasis. Our work revealed a higher susceptibility of C57BL/6 mice from the SPF2 facility in relation to C57BL/6 mice from the SPF1 facility. In confirmation with our first series of experiments, that demonstrated a central role of the host intestinal microbiota in regulating the immune responses, the pathology, and the survival of the host during schistosomiasis, the second series of experiments further presented an ameliorated immunological, pathological and vital prognosis of vulnerable SPF2 C57BL/6 mice receiving the intestinal microbiota of more resistant SPF1 C57BL/6 mice. Therefore, the study demonstrates the genetic regulation of gut microbiota which in turn, and/or in concert with the genetic make-up, influence the immunological, pathological, and vital host response during chronic schistosomiasis. The present work expands the conventional knowledge on schistosomiasis disease regulation and presents the gene-microbiota-immune-response interactome as a core piece of the regulatory machinery of this infection as exploitable to alter disease progression in the context of drug and vaccine development. 2021-09-14T18:08:16Z 2021-09-14T18:08:16Z 2021 2021-09-14T07:43:36Z Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/33888 eng application/pdf Department of Pathology Faculty of Health Sciences
spellingShingle Pathology
Mpotje, Thabo Rantanta Victor
The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
thesis_degree_str Doctoral
title The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
title_full The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
title_fullStr The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
title_full_unstemmed The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
title_short The role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
title_sort role of host and microbial factors in the pathogenesis of chronic schistosomiasis in mice
topic Pathology
url http://hdl.handle.net/11427/33888
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