首页> 美国卫生研究院文献>Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians Inc >Validation of two multiplex real-time PCR assays based on single nucleotide polymorphisms of the HA1 gene of equine influenza A virus in order to differentiate between clade 1 and clade 2 Florida sublineage isolates
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Validation of two multiplex real-time PCR assays based on single nucleotide polymorphisms of the HA1 gene of equine influenza A virus in order to differentiate between clade 1 and clade 2 Florida sublineage isolates

机译:基于马甲型流感病毒HA1基因单核苷酸多态性的两个多重实时PCR分析的验证以便区分进化枝1和进化枝2佛罗里达亚系分离株

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摘要

We validated 2 multiplex real-time PCR (rtPCR) assays based on single nucleotide polymorphisms (SNPs) of the hemagglutinin-1 ( ) gene of H3N8 equine influenza A virus (EIV) to determine clade affiliation of prototype and field isolates. Initial validation of the 2 multiplex rtPCR assays (SNP1 and SNP2) was performed using nucleic acid from 14 EIV Florida sublineage clade 1 and 2 prototype strains. We included in our study previously banked EIV rtPCR-positive nasal secretions from 341 horses collected across the United States in 2012–2017 to determine their clade affiliation. All 14 EIV prototype strains were identified correctly as either Florida sublineage clade 1 or clade 2 using the 2 SNP target positions. Of 341 EIV rtPCR-positive samples, 337 (98.8%) and 4 (1.2%) isolates were classified as belonging to clade 1 and 2 Florida sublineage EIV, respectively. All clade 1 Florida sublineage EIV strains were detected in domestic horses, three clade 2 Florida sublineage EIV strains originated from horses recently imported into the United States, and one clade 2 Florida sublineage EIV strain originated from a healthy horse recently vaccinated with a modified-live intranasal EIV vaccine containing the American lineage strain A/eq/Kentucky/1991. EIV Florida sublineage clade differentiation using a fast and reliable multiplex rtPCR platform will help monitor the introduction of clade 2 Florida sublineage EIV strains into North America via international transportation.
机译:我们基于H3N8马甲型流感病毒(EIV)的血凝素1()基因的单核苷酸多态性(SNP)验证了2种多重实时PCR(rtPCR)测定,以确定原型和现场分离株的进化枝隶属关系。使用来自14个EIV Florida亚系进化枝1和2个原型菌株的核酸,对2种多重rtPCR分析(SNP1和SNP2)进行了初步验证。我们在我们的研究中纳入了之前在2012-2017年间从美国各地收集的341匹马的EIV rtPCR阳性鼻分泌物,以确定它们的进化枝隶属关系。使用2个SNP目标位置,可以将所有14种EIV原型菌株正确鉴定为佛罗里达亚系进化枝1或进化枝2。在341个EIV rtPCR阳性样品中,分别有337个(98.8%)和4个(1.2%)分离株分别属于进化枝1和2佛罗里达亚谱系EIV。在家养的马匹中检测到所有进化枝1佛罗里达亚谱系EIV株,其中3进化枝2佛罗里达亚谱系EIV株起源于最近进口到美国的马匹,一种进化枝2佛罗里达亚谱系EIV株起源于最近接种了改良活疫苗的健康马含有美国谱系菌株A / eq / Kentucky / 1991的鼻内IVV疫苗。使用快速可靠的多重rtPCR平台对EIV佛罗里达亚系进化枝进行分化,将有助于监测通过国际运输将2种佛罗里达亚系EIV菌株引入北美的情况。

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