Chumbe Ana, Izquierdo-Lara Ray, Tataje Luis, Gonzalez Rosa, Cribillero Giovana, González Armando E, Fernández-Díaz Manolo, Icochea Eliana
A FARVET S.A.C., Chincha Alta, Ica, Peru.
B Laboratory of Avian Pathology, Universidad Nacional Mayor de San Marcos, School of Veterinary Medicine, San Borja, Lima, Peru.
Avian Dis. 2017 Mar;61(1):16-24. doi: 10.1637/11456-062016-Reg.
Infections of poultry with virulent strains of avian paramyxovirus 1 (APMV-1), also known as Newcastle disease viruses (NDVs), cause Newcastle disease (ND). This highly contagious disease affects poultry and many other species of birds worldwide. In countries where the disease is prevalent, constant monitoring and characterization of isolates causing outbreaks are necessary. In this study, we report the results of pathogenicity testing and phylogenetic analyses of seven NDVs isolated from several regions of Peru between 2004 and 2015. Six viruses had intracerebral pathogenicity indices (ICPIs) of between 1.75 and 1.88, corresponding to a velogenic pathotype. The remaining virus had an ICPI of 0.00, corresponding to a lentogenic pathotype. These results were consistent with amino acid sequences at the fusion protein (F) cleavage site. All velogenic isolates had the polybasic amino acid sequence RRQKR↓F at the F cleavage site. Phylogenetic analyses of complete F gene sequences showed that all isolates are classified in class II of APMV-1. The velogenic viruses are classified in genotype XII, while the lentogenic virus is classified in genotype II, closely related to the LaSota vaccine strain. Moreover, tree topology, bootstrap values, and genetic distances observed within genotype XII resulted in the identification of novel subgenotypes XIIa (in South America) and XIIb (in China) and possibly two clades within genotype XIIa. All velogenic Peruvian viruses belonged to subgenotype XIIa. Overall, our results confirm the presence of genotype XII in Peru and suggest that it is the prevalent genotype currently circulating in our country. The phylogenetic characterization of these isolates helps to characterize the evolution of NDV and may help with the development of vaccines specific to our regional necessities.
家禽感染1型禽副黏病毒(APMV-1)的强毒株,即新城疫病毒(NDV),会引发新城疫(ND)。这种高度传染性疾病影响着全球的家禽及许多其他鸟类物种。在该病流行的国家,持续监测和鉴定引发疫情的分离株很有必要。在本研究中,我们报告了2004年至2015年间从秘鲁几个地区分离出的7株新城疫病毒的致病性测试和系统发育分析结果。6株病毒的脑内致病性指数(ICPI)在1.75至1.88之间,对应速发型致病型。其余1株病毒的ICPI为0.00,对应缓发型致病型。这些结果与融合蛋白(F)裂解位点的氨基酸序列一致。所有速发型分离株在F裂解位点都有多元氨基酸序列RRQKR↓F。对完整F基因序列的系统发育分析表明,所有分离株都被归类于APMV-1的II类。速发型病毒被归类于基因型XII,而缓发型病毒被归类于基因型II,与LaSota疫苗株密切相关。此外,在基因型XII中观察到的树形拓扑结构、自展值和遗传距离,导致鉴定出新型亚基因型XIIa(在南美洲)和XIIb(在中国),并且在基因型XIIa内可能有两个分支。所有秘鲁的速发型病毒都属于亚基因型XIIa。总体而言,我们的结果证实了秘鲁存在基因型XII,并表明它是目前在我国流行的主要基因型。这些分离株的系统发育特征有助于描述新城疫病毒的进化,并可能有助于开发符合我们地区需求的特定疫苗。