Delmarva (DMV1639) infectious bronchitis virus infection alters the microbiome of gastrointestinal and respiratory tracts of broiler chickens

IF 2.4 3区 医学 Q3 VIROLOGY Virology Pub Date : 2025-03-01 Epub Date: 2025-01-23 DOI:10.1016/j.virol.2025.110428
Heshanthi Herath Mudiyanselage , Ahmed Ali , Motamed Elsayed Mohmoud , Muhammad Farooq , Ishara M. Isham , Awais Ghaffar , Juan Jovel , Susantha M. Gomis , Dongyan Niu , Mohamed Faizal Abdul-Careem
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Abstract

Infectious bronchitis virus (IBV) is known to cause significant alterations in tracheal microbial flora in broiler chickens 5 days post-infection (dpi) and our focus is to understand the changes in both respiratory and gastrointestinal microbiome in broilers over a period of time following IBV infection. A study was conducted to characterize the tracheal and cecal microbiome in IBV infected and control broiler chickens at 6, 9 and 15 dpi. IBV genome in trachea, lung and cecal tonsils could be observed in the infected group at all the time points. Immune response parameters and histopathological lesion scores were significantly higher in IBV infected trachea and cecal tonsils at 6, 9 and 15 dpi compared to the controls. We observed that cecal microbial diversity (alpha diversity) was increased in the IBV infected group at 6 and 15 dpi. On the other hand, diversity (alpha diversity) of tracheal microbiome was elevated only at 9 dpi in the IBV infected group. Moreover, significant shift of microbial communities (beta diversity), in both cecum and trachea was observed following IBV infection. Enzyme and metabolic pathway analyses of cecum indicated an upregulation of DNA replication and cell wall synthesis pathways and a downregulation of pathways related to short chain fatty acid (SCFA) production in the IBV infected group compared to the controls. Analysis of tracheal metabolic pathways suggested initial adaptation to the infection stress and gradually shifting to enhanced microbial growth and stability. The study outcome adds to the understanding of microbiome changes secondary to histological changes and immune response following IBV infection in broiler chickens.
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德尔玛瓦(DMV1639)传染性支气管炎病毒感染可改变肉鸡胃肠道和呼吸道的微生物群。
已知传染性支气管炎病毒(IBV)在感染后5天(dpi)引起肉鸡气管微生物群的显著改变,我们的重点是了解IBV感染后一段时间内肉鸡呼吸道和胃肠道微生物群的变化。研究了IBV感染肉鸡和对照肉鸡在6、9和15 dpi时的气管和盲肠微生物组特征。感染组在各时间点均可观察到气管、肺和盲肠扁桃体的IBV基因组。与对照组相比,IBV感染的气管和盲肠扁桃体在6、9和15 dpi时的免疫反应参数和组织病理学病变评分显著高于对照组。我们观察到IBV感染组在6和15 dpi时盲肠微生物多样性(α多样性)增加。另一方面,IBV感染组气管微生物组的多样性(α多样性)仅在9 dpi时升高。此外,IBV感染后,盲肠和气管内的微生物群落(β多样性)发生了显著变化。盲肠酶和代谢途径分析表明,与对照组相比,IBV感染组的DNA复制和细胞壁合成途径上调,与短链脂肪酸(SCFA)产生相关的途径下调。对气管代谢途径的分析表明,最初是适应感染压力,逐渐转向增强微生物生长和稳定性。本研究结果有助于理解IBV感染肉鸡后继发于组织学变化和免疫反应的微生物组变化。
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来源期刊
Virology
Virology 医学-病毒学
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
50 days
期刊介绍: Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.
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