Mancera Gracia Jose Carlos, Van den Hoecke Silvie, Saelens Xavier, Van Reeth Kristien
Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Center for Medical Biotechnology, VIB, Ghent, Belgium.
PLoS One. 2017 Apr 6;12(4):e0175267. doi: 10.1371/journal.pone.0175267. eCollection 2017.
H9N2 avian influenza viruses are endemic in poultry in Asia and the Middle East. These viruses sporadically cause dead-end infections in pigs and humans raising concerns about their potential to adapt to mammals or reassort with human or swine influenza viruses. We performed ten serial passages with an avian H9N2 virus (A/quail/Hong Kong/G1/1997) in influenza naïve pigs to assess the potential of this virus to adapt to swine. Virus replication in the entire respiratory tract and nasal virus excretion were examined after each passage and we deep sequenced viral genomic RNA of the parental and passage four H9N2 virus isolated from the nasal mucosa and lung. The parental H9N2 virus caused a productive infection in pigs with a predominant tropism for the nasal mucosa, whereas only 50% lung samples were virus-positive. In contrast, inoculation of pigs with passage four virus resulted in viral replication in the entire respiratory tract. Subsequent passages were associated with reduced virus replication in the lungs and infectious virus was no longer detectable in the upper and lower respiratory tract of inoculated pigs at passage ten. The broader tissue tropism after four passages was associated with an amino acid residue substitution at position 225, within the receptor-binding site of the hemagglutinin. We also compared the parental H9N2, passage four H9N2 and the 2009 pandemic H1N1 (pH1N1) virus in a direct contact transmission experiment. Whereas only one out of six contact pigs showed nasal virus excretion of the wild-type H9N2 for more than four days, all six contact animals shed the passage four H9N2 virus. Nevertheless, the amount of excreted virus was significantly lower when compared to that of the pH1N1, which readily transmitted and replicated in all six contact animals. Our data demonstrate that serial passaging of H9N2 virus in pigs enhances its replication and transmissibility. However, full adaptation of an avian H9N2 virus to pigs likely requires an extensive set of mutations.
H9N2禽流感病毒在亚洲和中东的家禽中呈地方流行性。这些病毒偶尔会在猪和人类中引起终末感染,这引发了人们对其适应哺乳动物或与人类或猪流感病毒重配的潜力的担忧。我们用一种禽H9N2病毒(A/鹌鹑/香港/G1/1997)在未感染流感的猪中进行了十次连续传代,以评估该病毒适应猪的潜力。每次传代后检查整个呼吸道中的病毒复制情况和鼻腔病毒排泄情况,并对从鼻黏膜和肺部分离的亲代和传代4的H9N2病毒的病毒基因组RNA进行深度测序。亲代H9N2病毒在猪中引起了有生产性的感染,主要嗜性为鼻黏膜,而只有50%的肺样本病毒呈阳性。相比之下,用传代4病毒接种猪导致病毒在整个呼吸道中复制。随后的传代与肺中病毒复制减少有关,在传代10时,接种猪的上、下呼吸道中不再能检测到感染性病毒。传代4后更广泛的组织嗜性与血凝素受体结合位点内第225位的氨基酸残基取代有关。我们还在直接接触传播实验中比较了亲代H9N2、传代4的H9N2和2009年大流行H1N1(pH1N1)病毒。虽然六只接触猪中只有一只显示野生型H9N2的鼻腔病毒排泄持续超过四天,但所有六只接触动物都排出了传代4的H9N2病毒。然而,与pH1N1相比,排出的病毒量显著较低,pH1N1在所有六只接触动物中都能轻易传播和复制。我们的数据表明,H9N2病毒在猪中的连续传代增强了其复制和传播能力。然而,禽H9N2病毒完全适应猪可能需要一系列广泛的突变。