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Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation

Baylisascaris schroederi, a roundworm (ascaridoid) parasite specific to the bamboo-feeding giant panda (Ailuropoda melanoleuca), represents a leading cause of mortality in wild giant panda populations. Here, we present a 293-megabase chromosome-level genome assembly of B. schroederi to infer its bio...

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Autores principales: Xie, Yue, Wang, Sen, Wu, Shuangyang, Gao, Shenghan, Meng, Qingshu, Wang, Chengdong, Lan, Jingchao, Luo, Li, Zhou, Xuan, Xu, Jing, Gu, Xiaobin, He, Ran, Yang, Zijiang, Peng, Xuerong, Hu, Songnian, Yang, Guangyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684166/
https://www.ncbi.nlm.nih.gov/pubmed/34487863
http://dx.doi.org/10.1016/j.gpb.2021.08.002
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author Xie, Yue
Wang, Sen
Wu, Shuangyang
Gao, Shenghan
Meng, Qingshu
Wang, Chengdong
Lan, Jingchao
Luo, Li
Zhou, Xuan
Xu, Jing
Gu, Xiaobin
He, Ran
Yang, Zijiang
Peng, Xuerong
Hu, Songnian
Yang, Guangyou
author_facet Xie, Yue
Wang, Sen
Wu, Shuangyang
Gao, Shenghan
Meng, Qingshu
Wang, Chengdong
Lan, Jingchao
Luo, Li
Zhou, Xuan
Xu, Jing
Gu, Xiaobin
He, Ran
Yang, Zijiang
Peng, Xuerong
Hu, Songnian
Yang, Guangyou
author_sort Xie, Yue
collection PubMed
description Baylisascaris schroederi, a roundworm (ascaridoid) parasite specific to the bamboo-feeding giant panda (Ailuropoda melanoleuca), represents a leading cause of mortality in wild giant panda populations. Here, we present a 293-megabase chromosome-level genome assembly of B. schroederi to infer its biology, including host adaptations. Comparative genomics revealed an evolutionary trajectory accompanied by host-shift events in ascaridoid parasite lineages after host separations, suggesting their potential for transmission and rapid adaptation to new hosts. Genomic and anatomical lines of evidence, including expansion and positive selection of genes related to the cuticle and basal metabolisms, indicate that B. schroederi undergoes specific adaptations to survive in the sharp-edged bamboo-enriched gut of giant pandas by structurally increasing its cuticle thickness and efficiently utilizing host nutrients through gut parasitism. Additionally, we characterized the secretome of B. schroederi and predicted potential drug and vaccine targets for new control strategies. Overall, this genome resource provides new insights into the host adaptation of B. schroederi to the giant panda as well as the host-shift events in ascaridoid parasite lineages. Our findings on the unique biology of B. schroederi will also aid in the development of prevention and treatment measures to protect giant panda populations from roundworm parasitism.
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spelling pubmed-96841662022-11-25 Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation Xie, Yue Wang, Sen Wu, Shuangyang Gao, Shenghan Meng, Qingshu Wang, Chengdong Lan, Jingchao Luo, Li Zhou, Xuan Xu, Jing Gu, Xiaobin He, Ran Yang, Zijiang Peng, Xuerong Hu, Songnian Yang, Guangyou Genomics Proteomics Bioinformatics Original Research Baylisascaris schroederi, a roundworm (ascaridoid) parasite specific to the bamboo-feeding giant panda (Ailuropoda melanoleuca), represents a leading cause of mortality in wild giant panda populations. Here, we present a 293-megabase chromosome-level genome assembly of B. schroederi to infer its biology, including host adaptations. Comparative genomics revealed an evolutionary trajectory accompanied by host-shift events in ascaridoid parasite lineages after host separations, suggesting their potential for transmission and rapid adaptation to new hosts. Genomic and anatomical lines of evidence, including expansion and positive selection of genes related to the cuticle and basal metabolisms, indicate that B. schroederi undergoes specific adaptations to survive in the sharp-edged bamboo-enriched gut of giant pandas by structurally increasing its cuticle thickness and efficiently utilizing host nutrients through gut parasitism. Additionally, we characterized the secretome of B. schroederi and predicted potential drug and vaccine targets for new control strategies. Overall, this genome resource provides new insights into the host adaptation of B. schroederi to the giant panda as well as the host-shift events in ascaridoid parasite lineages. Our findings on the unique biology of B. schroederi will also aid in the development of prevention and treatment measures to protect giant panda populations from roundworm parasitism. Elsevier 2022-04 2021-09-03 /pmc/articles/PMC9684166/ /pubmed/34487863 http://dx.doi.org/10.1016/j.gpb.2021.08.002 Text en © 2021 Beijing Institute of Genomics https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research
Xie, Yue
Wang, Sen
Wu, Shuangyang
Gao, Shenghan
Meng, Qingshu
Wang, Chengdong
Lan, Jingchao
Luo, Li
Zhou, Xuan
Xu, Jing
Gu, Xiaobin
He, Ran
Yang, Zijiang
Peng, Xuerong
Hu, Songnian
Yang, Guangyou
Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation
title Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation
title_full Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation
title_fullStr Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation
title_full_unstemmed Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation
title_short Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation
title_sort genome of the giant panda roundworm illuminates its host shift and parasitic adaptation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684166/
https://www.ncbi.nlm.nih.gov/pubmed/34487863
http://dx.doi.org/10.1016/j.gpb.2021.08.002
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