Seal Bruce S, Wise Mark G, Pedersen Janice C, Senne Dennis A, Alvarez Rene, Scott Melissa S, King Daniel J, Yu Qingzhong, Kapczynski Darrell R
Southeast Poultry Research Laboratory, U.S. Department of Agriculture, Agricultural Research Service, 934 College Station Road, Athens, GA 360605, USA.
Vet Microbiol. 2005 Mar 20;106(1-2):7-16. doi: 10.1016/j.vetmic.2004.11.013. Epub 2005 Jan 28.
Avian paramyxovirus 1 (APMV-1), also referred to as Newcastle disease virus (NDV), variants of low virulence were isolated from chickens, ducks and other unidentified species found in live-bird markets of the northeastern United States. These isolates were characterized as APMV-1 by the hemagglutination-inhibition (HI) assay utilizing NDV-specific polyclonal antisera. However, the isolates failed to react with a monoclonal antibody that has specificity for a wide variety of APMV-1 isolates. Although only highly virulent isolates require reporting to international regulatory agencies, the ability to correctly identify APMV-1 types is important for control and regulatory purposes. Protein gel patterns of the purified isolates resembled previously reported APMV-1 and anti-NDV polyclonal sera recognized the viral proteins. For three isolates oligonucleotide primers specific for the nucleoprotein, fusion protein and polymerase genes of NDV were utilized to synthesize cDNA using viral RNA as a template. Approximately 12kb of the genome was subsequently sequenced for the three isolates that included the nucleoprotein, phosphoprotein, matrix protein, fusion (F) protein, hemagglutinin-neuraminidase protein genes and a 5' portion of the polymerase gene. The isolates had an F protein cleavage site sequence of ERQER/LVG indicating low-virulence viruses that phylogenetically separated with other unique NDV isolates designated as a lineage 6 genotype. Additionally, a four amino acid insert was detected in the predicted phosphoprotein which complies with the "rule of six" among paramyxoviruses. These APMV-1 genotypes have not been previously reported in North America and further substantiate the heterogeneous genetic nature of these commercially important pathogens found worldwide.
禽副粘病毒1型(APMV-1),也被称为新城疫病毒(NDV),从美国东北部活禽市场的鸡、鸭及其他未明确的物种中分离出了低毒力变种。利用新城疫病毒特异性多克隆抗血清通过血凝抑制(HI)试验将这些分离株鉴定为APMV-1。然而,这些分离株未能与对多种APMV-1分离株具有特异性的单克隆抗体发生反应。虽然只有高毒力分离株需要向国际监管机构报告,但正确鉴定APMV-1类型的能力对于控制和监管目的很重要。纯化分离株的蛋白质凝胶图谱与先前报道的APMV-1相似,抗新城疫病毒多克隆血清能识别病毒蛋白。对于三个分离株,利用针对新城疫病毒核蛋白、融合蛋白和聚合酶基因的寡核苷酸引物,以病毒RNA为模板合成cDNA。随后对这三个分离株约12kb的基因组进行了测序,包括核蛋白、磷蛋白、基质蛋白、融合(F)蛋白、血凝素神经氨酸酶蛋白基因以及聚合酶基因的5'端部分。这些分离株的F蛋白裂解位点序列为ERQER/LVG,表明是低毒力病毒,在系统发育上与其他被指定为6型基因型的独特新城疫病毒分离株分开。此外,在预测的磷蛋白中检测到一个四氨基酸插入,这符合副粘病毒中的“六规则”。这些APMV-1基因型此前在北美尚未有报道,进一步证实了这些在全球范围内具有商业重要性的病原体的遗传异质性。