Spatz Stephen J, Garcia Maricarmen, Riblet Sylva, Ross Teresa A, Volkening Jeremy D, Taylor Tonya L, Kim Taejoong, Afonso Claudio L
a United States Department of Agriculture , Agricultural Research Service, US National Poultry Research Center , USDA ARS USNPRC, Athens , GA , USA.
b Department of Population Health , College of Veterinary Medicine, Poultry Diagnostic and Research Center, University of Georgia , Athens , GA , USA.
Avian Pathol. 2019 Jun;48(3):255-269. doi: 10.1080/03079457.2019.1579298. Epub 2019 Mar 11.
Over the last decade the US broiler industry has fought long-lasting outbreaks of infectious laryngotracheitis (ILTV). Previously, nine genotypes (I-IX) of ILTVs have been recognized using the polymerase chain reaction-restriction fragment length polymorphisms (PCR-RFLP) method with three viral alleles (gB, gM and UL47/gG). In this study, the genotyping system was simplified to six genotypes by amplicon sequencing and examining discriminating single nucleotide polymorphisms (SNPs) within these open reading frames. Using phylogenomic analysis of 27 full genomes of ILTV, a single allele (ORF A/ORF B) was identified containing SNPs that could differentiate ILTVs into genotypes congruent with the phylogenetic partitioning. The allelic variations allowed for the cataloging of the 27 strains into 5 genotypes: vaccinal TCO, vaccinal CEO, virulent CEO-like, virulent US and virulent US backyard flocks from 1980 to 1990, correlating with the PCR-RFLP genotypes I/ II/ III (TCO), IV (CEO), V (virulent CEO-like), VI (virulent US) and VII/VIII/IX (virulent US backyard flock isolates). With the unique capabilities of third generation sequencing, we investigated the application of Oxford Nanopore MinION technology for rapid sequencing of the amplicons generated in the single-allele assay. This technology was an improvement over Sanger-based sequencing of the single allele amplicons due to a booster amplification step in the MinION sequencing protocol. Overall, there was a 90% correlation between the genotyping results of the single-allele assay and the multi-allele assay. Surveillance of emerging ILTV strains could greatly benefit from real-time amplicon sequencing using the single-allele assay and MinION sequencing. RESEARCH HIGHLIGHTS A multi-allelic assay identified nine ILTV genotypes circulating in the US Single-allele genotyping is congruent with whole genome phylogenetic partitioning US ILTV strains can be grouped into five genotypes using the single-allele assay The single-allele assay can be done using MinION sequencing of barcoded amplicons.
在过去十年中,美国肉鸡产业一直在应对传染性喉气管炎病毒(ILTV)的长期疫情。此前,利用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,结合三个病毒等位基因(gB、gM和UL47/gG),已识别出ILTV的九种基因型(I-IX)。在本研究中,通过扩增子测序并检查这些开放阅读框内具有区分性的单核苷酸多态性(SNP),将基因分型系统简化为六种基因型。利用对27个ILTV全基因组的系统发育基因组分析,鉴定出一个单一等位基因(ORF A/ORF B),其包含的SNP可将ILTV分为与系统发育划分一致的基因型。等位基因变异使得这27个毒株可被归类为5种基因型:疫苗株TCO、疫苗株CEO、强毒株CEO样、强毒株美国株以及1980年至1990年的强毒株美国后院鸡群毒株,这与PCR-RFLP基因型I/II/III(TCO)、IV(CEO)、V(强毒株CEO样)、VI(强毒株美国株)和VII/VIII/IX(强毒株美国后院鸡群分离株)相关。借助第三代测序的独特功能,我们研究了牛津纳米孔MinION技术在单等位基因检测中对扩增子进行快速测序的应用。由于MinION测序方案中的增强扩增步骤,该技术相较于基于桑格法的单等位基因扩增子测序有了改进。总体而言,单等位基因检测与多等位基因检测的基因分型结果之间存在90%的相关性。对新兴ILTV毒株的监测可通过使用单等位基因检测和MinION测序的实时扩增子测序大大受益。研究亮点:多等位基因检测识别出在美国流行的九种ILTV基因型;单等位基因基因分型与全基因组系统发育划分一致;使用单等位基因检测可将美国ILTV毒株分为五种基因型;单等位基因检测可通过对条形码扩增子进行MinION测序来完成。