Full-length genome sequences of the first H9N2 avian influenza viruses isolated in the Northeast of Algeria

被引:16
作者
Barberis, Abdelheq [1 ,2 ]
Boudaoud, Amine [2 ]
Gorrill, Angelina [3 ]
Loupias, Josianne [3 ]
Ghram, Abdeljelil [4 ]
Lachheb, Jihene [4 ]
Alloui, Nadir [2 ]
Ducatez, Mariette F. [3 ]
机构
[1] Ctr Rech Biotechnol, Nouvelle Ville Ali Mendj, El Khroub, Algeria
[2] Univ Batna, ISVSA, LESPA, Dept Vet, Batna, Algeria
[3] Univ Toulouse, IHAP, INRAE, ENVT, 23 Chemin Capelles, F-31076 Toulouse, France
[4] Univ Tunis El Manar, Inst Pasteur Tunis, Lab Epidemiol & Microbiol Vet, Tunis, Tunisia
关键词
Algeria; Full-length genome sequencing; Phylogenetic analysis; Molecular characterization; AMINO-ACID SUBSTITUTION; N-LINKED GLYCOSYLATION; A VIRUS; RESPIRATORY VIRUSES; HEMAGGLUTININ GENE; ADAPTIVE MUTATIONS; MOLECULAR-CHANGES; BROILER FLOCKS; HIGH VIRULENCE; SUBTYPE H9N2;
D O I
10.1186/s12985-020-01377-z
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background H9N2 avian influenza viruses (AIV) has a worldwide geographic distribution and affects poultry of different types of production. H9N2 AIV was first reported in the Northeast of Algeria in April 2017, following an outbreak associated with high mortality, in broiler flocks. In the present study, we report full-length genome sequences of AIV H9N2, and the detailed phylogeny and molecular genetic analyses. Methods Ten AIV H9N2 strains, collected in broiler flocks, were amplified in 9-day-old embryonated specific pathogen free (SPF) chicken eggs. Their full-length genomes were successfully sequenced and phylogenetic and molecular characterizations were conducted. Results Phylogenetic analysis showed that the isolates were monophyletic, grouped within the G-1 lineage and were very close to Moroccan and Algerian strains identified in 2016 and 2017, respectively. The low pathogenicity of the strains was confirmed by the sequence motif (335RSSR/GLF341) at the hemagglutinin (HA) cleavage site. An exclusive substitution (T197A) that had not been previously reported for H9N2 viruses; but, conserved in some pandemic H1N1 viruses, was observed. When compared to the G1-like H9N2 prototype, the studied strains showed one less glycosylation site in HA, but 2-3 additional ones in the stalk of the neuraminidase (NA). The HA protein harbored the substitution 234 L, suggesting binding preference to human-like receptors. The NA protein harbored S372A and R403W substitutions, previously detected in H9N2 from Asia and the Middle East, and especially in H2N2 and H3N2 strains that caused human pandemics. Different molecular markers associated with virulence and mammalian infections have been detected in the viral internal proteins. The matrix M2 protein possessed the S31N substitution associated with drug resistance. The non-structural 1 (NS1) protein showed the "GSEV" PDZ ligand (PL) C-terminal motif and no 80-84 deletion. Conclusion Characterized Algerian AIV isolates showed mutations that suggest increased zoonotic potential. Additional studies in animal models are required to investigate the pathogenicity of these H9N2 AIV strains. Monitoring their evolution in both migratory and domestic birds is crucial to prevent transmission to humans. Implementation of adequate biosecurity measures that limit the introduction and the propagation of AIV H9N2 in Algerian poultry farm is crucial.
引用
收藏
页数:16
相关论文
共 98 条
[1]   Characterization of avian H9N2 influenza viruses from United Arab Emirates 2000 to 2003 [J].
Aamir, U. B. ;
Wernery, Ulrich ;
Ilyushina, N. ;
Webster, R. G. .
VIROLOGY, 2007, 361 (01) :45-55
[2]  
[Anonymous], 2013, DNA SEQ ASS V4, P2013
[3]   PB2 mutations arising during H9N2 influenza evolution in the Middle East confer enhanced replication and growth in mammals [J].
Arai, Yasuha ;
Kawashita, Norihito ;
Ibrahim, Madiha Salah ;
Elgendy, Emad Mohamed ;
Daidoji, Tomo ;
Ono, Takao ;
Takagi, Tatsuya ;
Nakaya, Takaaki ;
Matsumoto, Kazuhiko ;
Watanabe, Yohei .
PLOS PATHOGENS, 2019, 15 (07)
[4]   A Single Amino Acid Substitution in the Novel H7N9 Influenza A Virus NS1 Protein Increases CPSF30 Binding and Virulence [J].
Ayllon, Juan ;
Domingues, Patricia ;
Rajsbaum, Ricardo ;
Miorin, Lisa ;
Schmolke, Mirco ;
Hale, Benjamin G. ;
Garcia-Sastre, Adolfo .
JOURNAL OF VIROLOGY, 2014, 88 (20) :12146-12151
[5]   Influenza virus nucleoprotein interacts with influenza virus polymerase proteins [J].
Biswas, SK ;
Boutz, PL ;
Nayak, DP .
JOURNAL OF VIROLOGY, 1998, 72 (07) :5493-5501
[6]   PB2 Residue 271 Plays a Key Role in Enhanced Polymerase Activity of Influenza A Viruses in Mammalian Host Cells [J].
Bussey, Kendra A. ;
Bousse, Tatiana L. ;
Desmet, Emily A. ;
Kim, Baek ;
Takimoto, Toru .
JOURNAL OF VIROLOGY, 2010, 84 (09) :4395-4406
[7]   Avian influenza A (H9N2): computational molecular analysis and phylogenetic characterization of viral surface proteins isolated between 1997 and 2009 from the human population [J].
Butt, Azeem M. ;
Siddique, Samerene ;
Idrees, Muhammad ;
Tong, Yigang .
VIROLOGY JOURNAL, 2010, 7
[8]   H9N2 subtype influenza A viruses in poultry in Pakistan are closely related to the H9N2 viruses responsible for human infection in Hong Kong [J].
Cameron, KR ;
Gregory, V ;
Banks, J ;
Brown, IH ;
Alexander, DJ ;
Hay, AJ ;
Lin, YP .
VIROLOGY, 2000, 278 (01) :36-41
[9]   Genomic signatures of human versus avian influenza a viruses [J].
Chen, Guang-Wu ;
Chang, Shih-Cheng ;
Mok, Chee-Keng ;
Lo, Yu-Luan ;
Kung, Yu-Nong ;
Huang, Ji-Hung ;
Shih, Yun-Han ;
Wang, Ji-Yi ;
Chiang, Chiayn ;
Chen, Chi-Jene ;
Shih, Shin-Ru .
EMERGING INFECTIOUS DISEASES, 2006, 12 (09) :1353-1360
[10]  
Chen Yin, 2013, Zhonghua Liu Xing Bing Xue Za Zhi, V34, P604