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Molecular epidemiology and evolutionary histories of human coronavirus OC43 and HKU1 among patients with upper respiratory tract infections in Kuala Lumpur, Malaysia

机译:马来西亚吉隆坡上呼吸道感染患者中冠状病毒OC43和HKU1的分子流行病学和进化史

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Background Despite the worldwide circulation of human coronavirus OC43 (HCoV-OC43) and HKU1 (HCoV-HKU1), data on their molecular epidemiology and evolutionary dynamics in the tropical Southeast Asia region is lacking. Methods The study aimed to investigate the genetic diversity, temporal distribution, population history and clinical symptoms of betacoronavirus infections in Kuala Lumpur, Malaysia between 2012 and 2013. A total of 2,060 adults presented with acute respiratory symptoms were screened for the presence of betacoronaviruses using multiplex PCR. The spike glycoprotein, nucleocapsid and 1a genes were sequenced for phylogenetic reconstruction and Bayesian coalescent inference. Results A total of 48/2060 (2.4?%) specimens were tested positive for HCoV-OC43 (1.3?%) and HCoV-HKU1 (1.1?%). Both HCoV-OC43 and HCoV-HKU1 were co-circulating throughout the year, with the lowest detection rates reported in the October-January period. Phylogenetic analysis of the spike gene showed that the majority of HCoV-OC43 isolates were grouped into two previously undefined genotypes, provisionally assigned as novel lineage 1 and novel lineage 2. Sign of natural recombination was observed in these potentially novel lineages. Location mapping showed that the novel lineage 1 is currently circulating in Malaysia, Thailand, Japan and China, while novel lineage 2 can be found in Malaysia and China. Molecular dating showed the origin of HCoV-OC43 around late 1950s, before it diverged into genotypes A (1960s), B (1990s), and other genotypes (2000s). Phylogenetic analysis revealed that 27.3?% of the HCoV-HKU1 strains belong to genotype A while 72.7?% belongs to genotype B. The tree root of HCoV-HKU1 was similar to that of HCoV-OC43, with the tMRCA of genotypes A and B estimated around the 1990s and 2000s, respectively. Correlation of HCoV-OC43 and HCoV-HKU1 with the severity of respiratory symptoms was not observed. Conclusions The present study reported the molecular complexity and evolutionary dynamics of human betacoronaviruses among adults with acute respiratory symptoms in a tropical country. Two novel HCoV-OC43 genetic lineages were identified, warranting further investigation on their genotypic and phenotypic characteristics.
机译:背景技术尽管人类冠状病毒OC43(HCoV-OC43)和HKU1(HCoV-HKU1)在世界范围内流通,但缺乏有关其在热带东南亚地区的分子流行病学和进化动力学的数据。方法:本研究旨在调查2012年至2013年在马来西亚吉隆坡发生的β-冠状病毒感染的遗传多样性,时间分布,人口史和临床症状。通过多重筛查,共筛查了2,060名出现急性呼吸道症状的成年人是否存在β-冠状病毒。 PCR。穗糖蛋白,核衣壳和1a基因进行了测序,以进行系统发育重建和贝叶斯合并推断。结果总共对48/2060(2.4%)的样本进行了HCoV-OC43(1.3 %%)和HCoV-HKU1(1.1 %%)阳性测试。 HCoV-OC43和HCoV-HKU1全年都在流通,在10月至1月期间报告的检出率最低。对穗基因的系统发生分析表明,大多数HCoV-OC43分离株被分为两个以前未定义的基因型,临时指定为新谱系1和新谱系2。在这些潜在的新谱系中观察到自然重组的迹象。位置图谱显示,新世系1在马来西亚,泰国,日本和中国目前正在流行,而新世系2在马来西亚和中国可以找到。分子测年显示了HCoV-OC43的起源,大约在1950年代末,然后分化为A型(1960年代),B型(1990年代)和其他基因型(2000年代)。系统发育分析表明,HCoV-HKU1菌株的27.3%属于基因型A,而72.7%则属于基因型B。HCoV-HKU1的树根与HCoV-OC43相似,tMRCA分别为基因型A和B。估计分别在1990年代和2000年代左右。没有观察到HCoV-OC43和HCoV-HKU1与呼吸道症状的严重程度之间的相关性。结论本研究报告了热带国家成年人急性呼吸道症状中人β冠状病毒的分子复杂性和进化动力学。确定了两个新的HCoV-OC43遗传谱系,需要对其基因型和表型特征进行进一步研究。

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