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Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts

The human whipworm Trichuris trichiura infects 289 million people worldwide, resulting in substantial morbidity. Whipworm infections are difficult to treat due to low cure rates and high reinfection rates. Interactions between whipworm and its host’s intestinal microbiome present a potential novel t...

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Autores principales: Rosa, Bruce A., Snowden, Caroline, Martin, John, Fischer, Kerstin, Kupritz, Jonah, Beshah, Ethiopia, Supali, Taniawati, Gankpala, Lincoln, Fischer, Peter U., Urban, Joseph F., Mitreva, Makedonka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7991909/
https://www.ncbi.nlm.nih.gov/pubmed/33777847
http://dx.doi.org/10.3389/fcimb.2021.637570
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author Rosa, Bruce A.
Snowden, Caroline
Martin, John
Fischer, Kerstin
Kupritz, Jonah
Beshah, Ethiopia
Supali, Taniawati
Gankpala, Lincoln
Fischer, Peter U.
Urban, Joseph F.
Mitreva, Makedonka
author_facet Rosa, Bruce A.
Snowden, Caroline
Martin, John
Fischer, Kerstin
Kupritz, Jonah
Beshah, Ethiopia
Supali, Taniawati
Gankpala, Lincoln
Fischer, Peter U.
Urban, Joseph F.
Mitreva, Makedonka
author_sort Rosa, Bruce A.
collection PubMed
description The human whipworm Trichuris trichiura infects 289 million people worldwide, resulting in substantial morbidity. Whipworm infections are difficult to treat due to low cure rates and high reinfection rates. Interactions between whipworm and its host’s intestinal microbiome present a potential novel target for infection control or prevention but are very complicated and are identified using inconsistent methodology and sample types across the literature, limiting their potential usefulness. Here, we used a combined 16S rRNA gene OTU analysis approach (QIIME2) for samples from humans and mice infected with whipworm (T. trichiura and T. muris, respectively) to identify for the first time, bacterial taxa that were consistently associated with whipworm infection spanning host species and infection status using four independent comparisons (baseline infected vs uninfected and before vs after deworming for both humans and mice). Using these four comparisons, we identified significant positive associations for seven taxa including Escherichia, which has been identified to induce whipworm egg hatching, and Bacteroides, which has previously been identified as a major component of the whipworm internal microbiome. We additionally identified significant negative associations for five taxa including four members of the order Clostridiales, two from the family Lachnospiraceae, including Blautia which was previously identified as positively associated with whipworm in independent human and mouse studies. Using this approach, bacterial taxa of interest for future association and mechanistic studies were identified, and several were validated by RT-qPCR. We demonstrate the applicability of a mouse animal model for comparison to human whipworm infections with respect to whipworm-induced intestinal microbiome disruption and subsequent restoration following deworming. Overall, the novel cross-species analysis approach utilized here provides a valuable research tool for studies of the interaction between whipworm infection and the host intestinal microbiome.
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spelling pubmed-79919092021-03-26 Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts Rosa, Bruce A. Snowden, Caroline Martin, John Fischer, Kerstin Kupritz, Jonah Beshah, Ethiopia Supali, Taniawati Gankpala, Lincoln Fischer, Peter U. Urban, Joseph F. Mitreva, Makedonka Front Cell Infect Microbiol Cellular and Infection Microbiology The human whipworm Trichuris trichiura infects 289 million people worldwide, resulting in substantial morbidity. Whipworm infections are difficult to treat due to low cure rates and high reinfection rates. Interactions between whipworm and its host’s intestinal microbiome present a potential novel target for infection control or prevention but are very complicated and are identified using inconsistent methodology and sample types across the literature, limiting their potential usefulness. Here, we used a combined 16S rRNA gene OTU analysis approach (QIIME2) for samples from humans and mice infected with whipworm (T. trichiura and T. muris, respectively) to identify for the first time, bacterial taxa that were consistently associated with whipworm infection spanning host species and infection status using four independent comparisons (baseline infected vs uninfected and before vs after deworming for both humans and mice). Using these four comparisons, we identified significant positive associations for seven taxa including Escherichia, which has been identified to induce whipworm egg hatching, and Bacteroides, which has previously been identified as a major component of the whipworm internal microbiome. We additionally identified significant negative associations for five taxa including four members of the order Clostridiales, two from the family Lachnospiraceae, including Blautia which was previously identified as positively associated with whipworm in independent human and mouse studies. Using this approach, bacterial taxa of interest for future association and mechanistic studies were identified, and several were validated by RT-qPCR. We demonstrate the applicability of a mouse animal model for comparison to human whipworm infections with respect to whipworm-induced intestinal microbiome disruption and subsequent restoration following deworming. Overall, the novel cross-species analysis approach utilized here provides a valuable research tool for studies of the interaction between whipworm infection and the host intestinal microbiome. Frontiers Media S.A. 2021-03-11 /pmc/articles/PMC7991909/ /pubmed/33777847 http://dx.doi.org/10.3389/fcimb.2021.637570 Text en Copyright © 2021 Rosa, Snowden, Martin, Fischer, Kupritz, Beshah, Supali, Gankpala, Fischer, Urban and Mitreva http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Rosa, Bruce A.
Snowden, Caroline
Martin, John
Fischer, Kerstin
Kupritz, Jonah
Beshah, Ethiopia
Supali, Taniawati
Gankpala, Lincoln
Fischer, Peter U.
Urban, Joseph F.
Mitreva, Makedonka
Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts
title Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts
title_full Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts
title_fullStr Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts
title_full_unstemmed Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts
title_short Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts
title_sort whipworm-associated intestinal microbiome members consistent across both human and mouse hosts
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7991909/
https://www.ncbi.nlm.nih.gov/pubmed/33777847
http://dx.doi.org/10.3389/fcimb.2021.637570
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