Azeem Shahan, Baroch John, Tewari Deepanker, Pabilonia Kristy L, Killian Mary, Bradel-Tretheway Birgit, Sun Dong, Ghorbani-Nezami Sara, Yoon Kyoung-Jin
Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA 50011, USA.
Institute of Microbiology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan.
Pathogens. 2024 Apr 17;13(4):333. doi: 10.3390/pathogens13040333.
The surveillance of migratory waterbirds (MWs) for avian influenza virus (AIV) is indispensable for the early detection of a potential AIV incursion into poultry. Surveying AIV infections and virus subtypes in understudied MW species could elucidate their role in AIV ecology. Oropharyngeal-cloacal (OPC) swabs were collected from non-mallard MWs between 2006 and 2011. OPC swabs ( = 1158) that molecularly tested positive for AIV (Cts ≤ 32) but tested negative for H5 and H7 subtypes were selected for virus isolation (VI). The selected samples evenly represented birds from all four North American flyways (Pacific, Central, Mississippi, and Atlantic). Eighty-seven low pathogenic AIV isolates, representing 31 sites in 17 states, were recovered from the samples. All isolates belonged to the North American lineage. The samples representing birds from the Central Flyway had the highest VI positive rate (57.5%) compared to those from the other flyways (10.3-17.2%), suggesting that future surveillance can focus on the Central Flyway. Of the isolates, 43.7%, 12.6%, and 10.3% were obtained from blue-winged teal, American wigeon, and American black duck species, respectively. Hatch-year MWs represented the majority of the isolates (70.1%). The most common H and N combinations were H3N8 (23.0%), H4N6 (18.4%), and H4N8 (18.4%). The HA gene between non-mallard and mallard MW isolates during the same time period shared 85.5-99.5% H3 identity and 89.3-99.7% H4 identity. Comparisons between MW (mallard and non-mallard) and poultry H3 and H4 isolates also revealed high similarity (79.0-99.0% and 88.7-98.4%), emphasizing the need for continued AIV surveillance in MWs.
对候鸟进行禽流感病毒监测对于早期发现潜在的禽流感病毒传入家禽群体至关重要。研究未充分了解的候鸟物种中的禽流感病毒感染情况和病毒亚型,有助于阐明它们在禽流感病毒生态中的作用。在2006年至2011年期间,从非绿头鸭候鸟中采集了口咽泄殖腔拭子。选择那些经分子检测禽流感病毒呈阳性(Ct值≤32)但H5和H7亚型检测呈阴性的口咽泄殖腔拭子(n = 1158)进行病毒分离。所选样本均匀地代表了来自北美所有四条候鸟迁徙路线(太平洋、中部、密西西比和大西洋)的鸟类。从样本中分离出87株低致病性禽流感病毒,代表了17个州的31个地点。所有分离株均属于北美谱系。与来自其他迁徙路线的样本(10.3 - 17.2%)相比,代表中部迁徙路线鸟类的样本病毒分离阳性率最高(57.5%),这表明未来的监测可以集中在中部迁徙路线。在分离株中,分别有43.7%、12.6%和10.3%来自蓝翅鸭、美国黑鸭和美洲绿头鸭物种。当年幼鸟占分离株的大多数(70.1%)。最常见的H和N组合是H3N8(23.0%)、H4N6(18.4%)和H4N8(18.4%)。同一时期非绿头鸭和绿头鸭候鸟分离株之间的血凝素(HA)基因H3同一性为85.5 - 99.5%,H4同一性为89.3 - 99.7%。对候鸟(绿头鸭和非绿头鸭)与家禽的H3和H4分离株进行比较也显示出高度相似性(79.0 - 99.0%和88.7 - 98.4%),强调了对候鸟持续进行禽流感病毒监测的必要性。