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目的 为了掌握新疆维吾尔自治区外环境禽流感病毒潜在威胁和职业暴露人群潜在感染状况,并且对急性突发性传染病疫情及时进行监测预警。方法 血清样本数据与外环境样本均采集自2021–2024年新疆地区的监测点。前者来自家禽养殖、屠宰等职业暴露人群,采用既往检测的红细胞凝集抑制实验结果;后者所覆盖的样本种类包括笼具表面擦拭样本、禽类粪便样本、禽类饮用水样本、禽类清洗污水样本,以及禽肉宰杀和存放案板的表面擦拭样本等,我们对环境样本采用实时荧光定量PCR法对禽流感病毒亚型H5、H7、H9亚型的核酸检测并挑选阳性样本进行HA基因测序和遗传进化分析。结果 共收集血清样本3395份,总阳性率9.40%,其中H5亚型抗体阳性率在2024年显著上升至30.66%。外环境样本5135份,总阳性率20.66%,H9亚型为绝对优势亚型(17.57%)。笼具表面(26.06%)、禽类饮水(25.36%)、清洗污水(22.37%)为高风险污染环境。空间分布显示,阿克苏、伊犁、喀什等地因活禽交易活跃或地处候鸟迁徙通道,病毒污染及混合感染风险较高。基因进化分析显示,H9N2分离株属Y280-like分支,具备哺乳动物受体结合潜力;H5N1分离株属2.3.4.4b分支,与全球高致病性禽流感流行株高度同源。结论 2021-2024年新疆外环境禽流感病毒污染普遍,H9亚型为绝对优势株,笼具表面、禽类饮水、清洗污水为主要污染源。H5亚型于2024年活跃传播,分离株属全球流行的2.3.4.4b高致病性分支,候鸟迁徙存在输入风险。职业暴露人群H5抗体阳性率年内升至30.66%,感染风险持续存在。H9N2病毒已具备哺乳动物受体结合特征,提示跨种传播潜力。建议将高风险环境作为消毒重点,加强候鸟沿线及活禽集散地监测,做好职业人群防护,持续追踪病毒进化动态。
Abstract:Objective To understand the potential threat of avian influenza viruses in the external environment and the potential infection status of occupationally exposed populations in Xinjiang Region, China, so as to achieve timely surveillance and early warning for acute emerging infectious disease outbreaks. Methods Serum samples and environmental specimens were collected from surveillance sites in Xinjiang region from 2021 to 2024. Serum samples were obtained from occupationally exposed populations such as poultry breeders and slaughter workers, with antibody data derived from previous hemagglutination inhibition tests. Environmental samples included surface swabs of cages, poultry feces, poultry drinking water, washing sewage, and swabs from slaughtering and processing cutting boards. All environmental specimens were screened for H5, H7 and H9 avian influenza virus nucleic acids by real-time fluorescent quantitative PCR. Positive samples were further subjected to HA gene sequencing and phylogenetic analysis. Results A total of 3,395 serum samples were collected, with an overall positive rate of 9.40%. Among them, the positive rate of H5 subtype antibody increased significantly to 30.66% in 2024. Of 5,135 environmental samples, the overall positive rate was 20.66%, with H9 subtype as the predominant subtype(17.57%). High contamination were detected on cage surfaces(26.06%), in poultry drinking water(25.36%) and washing sewage(22.37%). Spatial distribution showed that Aksu, Ili, Kashgar and other regions with active live poultry trade or located on migratory bird migration routes had higher risks of viral contamination and co-infection. Phylogenetic analysis revealed that H9N2 isolates belonged to the Y280-like lineage with mammalian receptor binding potential, while H5N1 isolates fell into clade 2.3.4.4b, which was highly homologous to globally circulating highly pathogenic avian influenza strains. Conclusion Widespread environmental contamination by avian influenza viruses was found in Xinjiang region from 2021 to 2024, with H9 subtype as the dominant strain. Cage surfaces, poultry drinking water and washing sewage were the main contamination sources. The H5 subtype spread actively in 2024, and the isolates belonged to the globally prevalent clade 2.3.4.4b of highly pathogenic strains, indicating a potential risk of introduction via migratory birds. The H5 antibody positive rate in occupationally exposed populations rose to 30.66% within the year, suggesting a persistent infection risk. H9N2 viruses have acquired mammalian receptor binding characteristics, indicating potential for cross-species transmission. It is recommended to focus disinfection on high-risk environments, strengthen surveillance along migratory routes and live poultry distribution centers, improve protection for occupational populations, and continuously monitor viral evolutionary dynamics.
[1]Webster RG, Bean WJ, Gorman OT, et al. Evolution and ecology of influenza A viruses[J]. Microbiol Rev,1992, 56(1):152-179. DOI:10. 1128/mr. 56. 1. 152-179. 1992.
[2]Kayali G, Barbour E, Dbaibo G, et al. Evidence of infection with H4 and H11 avian influenza viruses among Lebanese chicken growers[J]. PLoS One, 2011, 6(10):e26818. DOI:10. 1371/journal. pone. 0026818.
[3]Tong S, Li Y, Rivailler P, et al. A distinct lineage of influenza A virus from bats[J]. Proc Natl Acad Sci U S A, 2012, 109(11):4269-4274. DOI:10. 1073/pnas. 1116200109.
[4]龙小凤.高致病性禽流感的流行病学特点及防控措施[J].北方牧业,2025(19):35.
[5]黄泽颖,王济民. 2004—2014年我国禽流感发生状况与特征分析[J].广东农业科学,2015, 42(4):93-98.DOI:10. 3969/j. issn. 1004-874X. 2015. 04. 018.
[6]Peacock TP, Moncla L, Dudas G, et al. The global H5N1 influenza panzootic in mammals[J]. Nature,2025, 637(8045):304-313. DOI:10. 1038/s41586-024-08054-z.
[7]Hew YL, Guinat C, Couty M, et al. Introduction and inter-species transmission dynamics of high pathogenicity avian influenza H5N1 viruses in Japan 2021–25[J].Virus Evol, 2026, 12(1):veag005. DOI:10. 1093/ve/veag005.
[8]Rolfes MA, Kniss K, Kirby MK, et al. Human infections with highly pathogenic avian influenza a(H5N1)viruses in the United States from March 2024to May 2025[J]. Nat Med, 2025, 31(11):3889-3898.DOI:10. 1038/s41591-025-03905-2.
[9]高枫,芮宝玲,樊旭成,等.乌鲁木齐市职业人群禽流感病毒感染及外环境禽流感病毒监测分析[J].职业与健康,2014, 30(6):750-751+754. DOI:10. 13329/j.cnki. zyyjk. 2014. 06. 027.
[10]Gao R, Cao B, Hu Y, et al. Human infection with a novel avian-origin influenza a(H7N9)virus[J]. N Engl J Med, 2013, 368(20):1888-1897. DOI:10. 1056/nejmoa1304459.
[11]郜振国,马合木提,赵俊,等. 2014—2018年新疆人感染H7N9禽流感分子流行病学特征分析[J].中国人兽共患病学报,2024, 40(8):774-781. DOI:10. 3969/j.issn. 1002-2694. 2024. 00. 108.
[12]Zhu Y, Cong Y, Sun Y, et al. Molecular patterns of matrix protein 1(M1):a strong predictor of adaptive evolution in H9N2 avian influenza viruses[J]. Proc Natl Acad Sci U S A, 2025, 122(9):e2423983122. DOI:10. 1073/pnas. 2423983122.
[13]Yang J, Li J, Sun J, et al. Genetic diversity of H9N2avian influenza viruses in poultry across China and implications for zoonotic transmission[J]. Nat Microbiol, 2025, 10(6):1378-1392. DOI:10. 1038/s41564-025-02002-x.
[14]Yang J, Chen X, Li X, et al. Global spread of H3subtype avian influenza viruses with an accelerated evolution after interspecies transmission[J]. J Infect,2025, 91(2):106542. DOI:10. 1016/j.jinf. 2025. 106542.
[15]Yamamoto Y, Nakamura K, Okamatsu M, et al. Avian influenza virus(H5N1)replication in feathers of domestic waterfowl[J]. Emerg Infect Dis, 2008, 14(1):149-151. DOI:10. 3201/eid1401. 071036.
[16]付小强,孙强,徐惠,等.湖北省鄂州市城乡活禽市场H9N2亚型禽流感病毒HA和NA基因生物学特征分析[J].病毒学报,2025, 41(4):1183-1189. DOI:10. 13242/j. cnki. bingduxuebao. 250042.
[17]Moatasim Y, Kandeil A, Mostafa A, et al. Single gene reassortment of highly pathogenic avian influenza A H5N1 in the low pathogenic H9N2 backbone and its impact on pathogenicity and infectivity of novel reassortant viruses[J]. Arch Virol, 2017, 162(10):2959-2969. DOI:10. 1007/s00705-017-3434-x.
[18]荣晓夙,李虎,马瑞杰,等. 2017—2020年新疆维吾尔自治区阿克苏地区外环境禽流感病毒监测分析[J].疾病监测,2022, 37(1):123-126. DOI:10. 3784/jbjc. 202104070172.
[19]张雪花,陆吉虎,华涛,等.通用型H5亚型禽流感病毒亚单位疫苗抗原表达和免疫效力研究[J].病毒学报,2019, 35(6):864-872. DOI:10. 13242/j. cnki.bingduxuebao. 003600.
[20]Zhang XS, Pebody R, De Angelis D, et al. The possible impact of vaccination for seasonal influenza on emergence of pandemic influenza via reassortment[J].PLoS One, 2014, 9(12):e114637. DOI:10. 1371/journal. pone. 0114637.
[21]MacMahon KL, Delaney LJ, Kullman G, et al.Protecting poultry workers from exposure to avian influenza viruses[J]. Public Health Reports®,2008,123(3):316-322. DOI:10. 1177/003335490812300311.
基本信息:
DOI:10.13242/j.cnki.bingduxuebao.260028
中图分类号:R511.7;R181.8
引用信息:
[1]拜热娜·伊力哈尔,李泉希,阿依巴提·湖阿提,等.2021-2024年新疆地区职业暴露人群血清学和外环境禽流感病毒监测结果分析[J].病毒学报,2026,42(04):1168-1178.DOI:10.13242/j.cnki.bingduxuebao.260028.
基金信息:
“天山英才”医药卫生高层次人才培养计划(项目号:TSYC202401B003),题目:基于现场宏基因组测序的急性呼吸道传染病病原识别及暴发分析流程的建立; 新疆重大需求人才支持计划(项目号:XJRC-2025-ZZB-ZDXQ-013),题目:基于传染病监测预警平台的防控体系研究及推广应用~~
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