Hewson K A, Browning G F, Devlin J M, Ignjatovic J, Noormohammadi A H
Department of Veterinary Science, The University of Melbourne, 250 Princes Highway, Werribee, Victoria 3030, Australia.
Aust Vet J. 2010 Oct;88(10):408-13. doi: 10.1111/j.1751-0813.2010.00622.x.
A real-time polymerase chain reaction (PCR)/high-resolution melt (HRM) curve analysis protocol was developed in our laboratory to differentiate infectious bronchitis (IB) virus reference strains. In the current study, this method was used to detect and classify IB viruses in field submissions.
Over an 11-month period samples from 40 cases of suspected IB virus were received and 17 submissions were positive for IB virus by polymerase chain reaction. HRM curve analysis classified each strain as subgroup 1, 2 or 3 strain (12 submissions) or a strain that was unable to be classified (5 submissions). The 3' untranslated region (UTR) and partial S1 gene nucleotide sequences for the 17 IB virus strains were determined and their identity with those of the relative reference strains compared to confirm the classifications generated using the HRM curve analysis.
Of the 12 IB field viruses classified as subgroup 1, 2, or 3 using HRM curve analysis, the 3'UTR and S1 gene nucleotide sequences had identities ≥99% with the respective subgroup reference strain. Analysis of the 3' UTR and S1 gene nucleotide sequences for the five IB virus strains that could not be classified indicated that four belonged to one of the subgroups, and one was a potential recombinant strain (between strains from subgroups 2 and 3). A novel recombinant strain was also detected.
HRM curve analysis can rapidly assign the majority of IB viruses present in field submissions to known subgroups. Importantly, HRM curve analysis also identified variant genotypes that require further investigation.
我们实验室开发了一种实时聚合酶链反应(PCR)/高分辨率熔解(HRM)曲线分析方法,用于区分传染性支气管炎(IB)病毒参考毒株。在本研究中,该方法用于检测和分类现场送检样本中的IB病毒。
在11个月的时间里,共收到40例疑似IB病毒病例的样本,其中17份样本经聚合酶链反应检测为IB病毒阳性。HRM曲线分析将每个毒株分类为1、2或3亚组毒株(12份样本)或无法分类的毒株(5份样本)。测定了17株IB病毒的3'非翻译区(UTR)和部分S1基因核苷酸序列,并将其与相关参考毒株的序列进行比较,以确认使用HRM曲线分析得出的分类结果。
在通过HRM曲线分析分类为1、2或3亚组的12株IB现场病毒中,3'UTR和S1基因核苷酸序列与各自亚组参考毒株的序列同一性≥99%。对5株无法分类的IB病毒的3'UTR和S1基因核苷酸序列分析表明,其中4株属于其中一个亚组,1株是潜在的重组毒株(介于2亚组和3亚组毒株之间)。还检测到一株新型重组毒株。
HRM曲线分析可以快速将现场送检样本中存在的大多数IB病毒归为已知亚组。重要的是,HRM曲线分析还鉴定出了需要进一步研究的变异基因型。