FEMS microbes Pub Date : 2025-02-03 eCollection Date: 2025-01-01 DOI:10.1093/femsmc/xtaf001
Samson Oladokun, Mohammadali Alizadeh, Amirul I Mallick, Fatemeh Fazel, Janan Shoja Doost, Katherine Blake, Myles St Denis, Sugandha Raj, Shayan Sharif
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摘要

禽流感病毒(AIV)对家禽和人类健康构成重大威胁。本研究采用 16S rRNA 基因测序法研究 H9N2 AIV 感染对鸡呼吸道微生物群的影响。总共 48 只一天龄无特定病原体的鸡被分配到六个组:对照组和五个感染后组(第 1、3、5、7 和 9 天)。经过 15 天的微生物群稳定期后,感染鸡通过眼部、鼻内和气管内途径接受病毒接种体(107 TCID50/ml)。对气管和支气管肺泡灌洗液样本进行了分析。与 d0 对照组相比,在感染后第 5、7 和 9 天观察到微生物群多样性显著减少。永久多变量方差分析证实,感染组和未感染组之间存在显著的贝塔多样性差异(P = 0.001)。从第 5 天到第 9 天,微生物的变化主要表现为变形菌增加、放线菌和固缩菌减少,以及菊形菌增加。d5时Ⅰ型干扰素(IFN-β)和蝰蛇素基因表达的升高与微生物群多样性的降低相吻合,突出了呼吸道微生物群在调节宿主对AIV H9N2感染的反应中的作用,并提出了呼吸道菌群失调的潜在生物标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influenza a virus subtype H9N2 infection induces respiratory microbiota dysbiosis in chickens via type-I interferon-mediated mechanisms.

Avian influenza virus (AIV) poses significant threats to poultry and human health. This study investigates the impact of H9N2 AIV infection on the respiratory microbiota of chickens using 16S rRNA gene sequencing. Total 48 one-day-old specific pathogen-free chickens were assigned to six groups: a control and five post-infection groups (days 1, 3, 5, 7, and 9). After a 15-day microbiota stabilization period, the infected chickens received a viral inoculum (107 TCID50/ml) via ocular, intra-nasal, and intra-tracheal routes. Tracheal and broncho-alveolar lavage samples were analyzed. Significant reductions in microbiota diversity were observed on days 5, 7, and 9 post-infection, compared to d0 controls. Permutational Multivariate Analysis of Variance confirmed significant beta diversity differences (P = 0.001) between infected and uninfected groups. The microbial shifts from d5 to d9 were marked by increased Proteobacteria, decreased Actinobacteria and Firmicutes, and a rise in Dickeya. Elevated type-I interferon (IFN-β) and viperin gene expression at d5 coincided with reduced microbiota diversity, highlighting the respiratory microbiota's role in modulating host responses to AIV H9N2 infection and suggesting potential biomarkers for respiratory dysbiosis.

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CiteScore
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