Co-infection of H9N2 subtype avian influenza virus and infectious bronchitis virus decreases SP-A expression level in chickens

被引:15
作者
Huang, Qi [1 ,2 ]
Wang, Kai [1 ,2 ]
Pan, Ling [1 ]
Qi, Kezong [1 ]
Liu, Hongmei [1 ]
Chen, Hongjun [2 ]
机构
[1] Anhui Agr Univ, Coll Anim Sci & Technol, Hefei 230036, Peoples R China
[2] Chinese Acad Agr Sci, Shanghai Vet Res Inst, Shanghai 200241, Peoples R China
基金
中国国家自然科学基金;
关键词
Chicken surfactant protein A; Immune response; Co-infection; H9N2 subtype avian influenza virus; Infectious bronchitis virus; SURFACTANT PROTEIN-A; INNATE IMMUNE PROTEINS; PULMONARY COLLECTINS; INFLAMMATORY RESPONSE; RESPIRATORY PATHOGENS; II CELLS; INHIBITION; MODULATE; DEFENSE; MECHANISM;
D O I
10.1016/j.vetmic.2017.02.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chicken surfactant protein A (cSP-A) is a collectin believed to play an important role in antiviral immunity. However, cSP-A expression in the respiratory tract of chickens after viral co-infection remains unclear. The aim of this study was the detection and charterization of cSP-A in co-infected chickens. For this purpose, four-week-old specific pathogen-free (SPF) chickens were divided into five groups and inoculated intranasally with H9N2 subtype avian influenza virus (AIV), infectious bronchitis virus (IBV), or Newcastle disease virus (NDV). Chickens were sacrificed at three days post inoculation, and the lung, trachea, and air sac samples were taken to determine histological changes and expression levels of cSP-A mRNA and cSP-A protein. The cSP-A mRNA and its protein were detected separately using real-time quantitative reverse transcriptional polymerase chain reaction (qRT-PCR), a sandwich enzyme-linked immunosorbent assay (S-ELISA), and an immunohistochemistry assay (IHC). In comparison, for the PBS group as the negative group and the NDV-infected group as the positive group, the histological changes showed that the lesions of the AIV+ IBV co-infected group were more serious compared to the AIV-infected group and the IBV-infected group. Consequently, the expression level of cSP-A in the AIV+ IBV co-infected group significantly decreased when compared to the AIV-infected group and the IBV-infected group by qRT-PCR, ELISA, and IHC analysis. The mechanism of the downregulation of SP-A expression level will be addressed in future. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:110 / 116
页数:7
相关论文
共 50 条
  • [21] Co-infection of H9N2 influenza virus and Pseudomonas aeruginosa contributes to the development of hemorrhagic pneumonia in mink
    Zhang Bo-shun
    Li, Li-juan
    Zhu Qian
    Wang Zhen
    Yuan Peng
    Zhou Guo-dong
    Shi Wen-jian
    Chu Xue-fei
    Jiang, Shijin
    Xie Zhi-jing
    VETERINARY MICROBIOLOGY, 2020, 240
  • [22] Predicting Avian Influenza Co-Infection with H5N1 and H9N2 in Northern Egypt
    Young, Sean G.
    Carrel, Margaret
    Malanson, George P.
    Ali, Mohamed A.
    Kayali, Ghazi
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2016, 13 (09):
  • [23] Epidemiological surveillance of H9N2 avian influenza virus infection among chickens in farms and backyards in Egypt 2015-2016
    El-Sayed, Moataz Mohamed
    Arafa, Abdel Satar
    Abdelmagid, Marwa
    Youssef, Ahmed Ibrahim
    VETERINARY WORLD, 2021, 14 (04) : 949 - 955
  • [24] Experimental Evaluation for the Dual Infection of Low Pathogenic Avian Influenza Virus H9N2 and Avian Pathogenic Escherichia Coli in Commercial Broiler Chickens
    Amer, Sameh Abdel-Moez
    Ahmed, Hagar Magdy
    Maatouq, Asmaa Mahmoud
    Abdelbaki, Mohamed Mahmoud
    EGYPTIAN JOURNAL OF VETERINARY SCIENCE, 2024, 55 (07): : 1985 - 1994
  • [25] Comparative trachea transcriptome analysis between avian infectious bronchitis virus and avian pathogenic E. coli individual infection and co-infection in SPF chickens
    Hashemi, S.
    Ghalyanchilangeroudi, A.
    Hosseini, S. M.
    Sheikhi, N.
    ACTA VIROLOGICA, 2020, 64 (04) : 457 - 469
  • [26] Pathology and molecular detection of influenza A subtype H9N2 virus in commercial poultry in Nigeria, 2024
    Akanbi, Olatunde Babatunde
    Alaka, Olugbenga Olayinka
    Olaifa, Olanrewaju Samuel
    Meseko, Clement A.
    Inuwa, Bitrus
    Ohore, Obokparo Godspower
    Tijani, Monsuru
    Jarikre, Theophilus
    Ola, Olawale
    Odita, Christianah
    Ahmed, James Saidu
    Fagbohun, Olusegun
    Oluwayelu, Daniel
    Daodu, Olufemi B.
    Oladele, Omolade
    Olapade, James
    Taiwo, Olusegun
    Muhammad, Maryam
    OPEN VETERINARY JOURNAL, 2024, 14 (09) : 2381 - 2391
  • [27] Increased Pulmonary Pneumococcal Clearance after Resolution of H9N2 Avian Influenza Virus Infection in Mice
    Li, Jingyun
    Wang, Hongyan
    Lian, Pengjing
    Bai, Yu
    Zhang, Zihui
    Zhao, Lihong
    Xu, Tong
    Qiao, Jian
    INFECTION AND IMMUNITY, 2021, 89 (06)
  • [28] Viral interference between H9N2-low pathogenic avian influenza virus and avian infectious bronchitis virus vaccine strain H120 in vivo
    Rim, Aouini
    Nacira, Laamiri
    Jihene, Nsiri
    Said, Salhi
    Khaled, Miled
    Ahmed, Rejab
    Abdeljelil, Ghram
    COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES, 2019, 65 : 219 - 225
  • [29] Evaluation of immunostimulatory effects of a commercial herbal extract on avian influenza subtype H9N2 and Newcastle disease vaccination in chickens
    Talazadeh, F.
    Mayahi, M.
    Fathi, M.
    JOURNAL OF THE HELLENIC VETERINARY MEDICAL SOCIETY, 2022, 73 (02): : 4023 - 4030
  • [30] Probiotic Lactobacilli Limit Avian Influenza Virus Subtype H9N2 Replication in Chicken Cecal Tonsil Mononuclear Cells
    Alqazlan, Nadiyah
    Alizadeh, Mohammadali
    Boodhoo, Nitish
    Taha-Abdelaziz, Khaled
    Nagy, Eva
    Bridle, Byram
    Sharif, Shayan
    VACCINES, 2020, 8 (04) : 1 - 16