Dairy cows develop protective immunity against reinfection with bovine H5N1 influenza virus

IF 20.5 1区 生物学 Q1 MICROBIOLOGY
Antonio Facciuolo, Lauren Aubrey, Ulises Barron-Castillo, Nathalie Berube, Carla Norleen, Shannon McCreary, Yanyun Huang, Natalia Pessoa, Leslie Macas Jacome, Samira Mubareka, Allison McGeer, Yohannes Berhane, Volker Gerdts, Andrew Van Kessel, Bryce Warner, Yan Zhou
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Abstract

Infection of highly pathogenic avian influenza (HPAI) H5N1 clade 2.3.4.4b in dairy cows causes severe mastitis and milk production losses. Whether cows can develop protective immunity is unclear. Here we infected three lactating cows with HPAI H5N1 genotype B3.13 via the hindquarters of the udder to mimic intra-mammary infection. Inoculated cows displayed clinical responses consistent with affected dairy herds in the United States including virus shedding almost exclusively in inoculated hindquarters that peaked between Days 2–4 post inoculation and gradually declined by Day 21. Histologically, peak virus shedding in milk corresponded with severe acute necrotic mastitis in the inoculated hindquarters but not in the uninoculated forequarters. Two cows were reinfected with HPAI H5N1 virus at unaffected forequarters following resolution of infection. Secondary inoculation did not result in clinical manifestations or virus shedding in milk. Virus-neutralizing antibodies were detected at Day 14 post inoculation in milk with higher titres observed in the inoculated hindquarters relative to the forequarters. We also detected HPAI H5N1 viral RNA in air samples from animal rooms during routine husbandry activity. These data indicate that primary infection via intra-mammary inoculation can generate protective immunity against bovine HPAI H5N1 virus in dairy cows.

Abstract Image

奶牛对牛H5N1流感病毒的再感染产生保护性免疫
奶牛感染高致病性禽流感(HPAI) H5N1分支2.3.4.4b可导致严重的乳腺炎和产奶量损失。奶牛是否能产生保护性免疫尚不清楚。本研究用HPAI H5N1基因型B3.13感染了3头泌乳奶牛,通过乳房后臀模拟乳腺内感染。接种的奶牛表现出与美国受感染奶牛群一致的临床反应,包括病毒几乎完全在接种后2-4天达到高峰,到第21天逐渐下降。组织学上,乳汁中病毒脱落高峰与接种后臀的严重急性坏死性乳腺炎相对应,而与未接种前臀无关。在感染得到解决后,两头奶牛在未受影响的前肢再次感染了高致病性H5N1病毒。二次接种未引起临床表现或病毒在乳汁中脱落。接种后第14天,在乳汁中检测到病毒中和抗体,接种后后腿的抗体效价高于前肢。我们还在常规饲养活动期间从动物房间采集的空气样本中检测到高致病性H5N1病毒RNA。这些数据表明,通过乳内接种的初次感染可在奶牛中产生对牛高致病性H5N1病毒的保护性免疫。
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来源期刊
Nature Microbiology
Nature Microbiology Immunology and Microbiology-Microbiology
CiteScore
44.40
自引率
1.10%
发文量
226
期刊介绍: Nature Microbiology aims to cover a comprehensive range of topics related to microorganisms. This includes: Evolution: The journal is interested in exploring the evolutionary aspects of microorganisms. This may include research on their genetic diversity, adaptation, and speciation over time. Physiology and cell biology: Nature Microbiology seeks to understand the functions and characteristics of microorganisms at the cellular and physiological levels. This may involve studying their metabolism, growth patterns, and cellular processes. Interactions: The journal focuses on the interactions microorganisms have with each other, as well as their interactions with hosts or the environment. This encompasses investigations into microbial communities, symbiotic relationships, and microbial responses to different environments. Societal significance: Nature Microbiology recognizes the societal impact of microorganisms and welcomes studies that explore their practical applications. This may include research on microbial diseases, biotechnology, or environmental remediation. In summary, Nature Microbiology is interested in research related to the evolution, physiology and cell biology of microorganisms, their interactions, and their societal relevance.
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