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Molecular epidemiology of Rotavirus causing diarrhea among children less than five years of age visiting national level children hospitals, Nepal

机译:轮状病毒的分子流行病学造成近五年的儿童腹泻,尼泊尔儿童近期儿童医院

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Background Rotaviruses are the major cause of diarrhea among the infants and young children all over the world causing over 500,000 deaths and 2.4 million hospitalizations each year. In Nepal Rotavirus infection positivity rates ranges from 17.0 to 39.0% among children less than 5?years. However, little is known about the molecular genotypes of Rotavirus prevailing. The objective of this study was to estimate the burden of Rotavirus gastroenteritis and determine the genotypes of Rotavirus among children less than 5 years. Methods The cross sectional study was conducted from January to November 2014 among children less than 5 years old visiting Kanti Children’s Hospital and Tribhuvan University Teaching Hospital. Rotavirus antigen detection was performed by Enzyme Linked Immunosorbent Assay (ELISA) using ProSpecT Rotavirus Microplate Assay. Among the Rotavirus antigen positive samples, 59 samples were used for Rotavirus RNA extraction. Multiplex PCR was performed to identify G type comprising G1-G4, G8-G10 and G12 and P type comprising P[4], P[6], P[8], P[9], P[10], and P[11]. Results A total of 717 diarrheal stool samples were collected from patients ranging from 10?days to 59?months of age. Rotavirus antigen positive was found among ( N =?164)22.9% of patients. The highest number of the diarrhea was seen in January. Molecular analysis of Rotavirus genotypes revealed that the predominant G-Type was G12 (36%) followed by G9 (31%), G1 (21%), G2 (8.6%). The predominant P- type was P6 (32.8%) followed by P8 (31%), P10 (14.8%), P4 (14.8%). A total of seven G/P type combinations were identified the most common being G12P [6] (35.8%), G1P [8] (15.1%), G9P [8] (15.1%). Conclusion Rotavirus diarrhea is, mostly affecting children from 7 to 24?months in Nepal, mostly occurring in winter. The circulating genotypes in the country are found to be primarily unusual genotypes and predominance of G12P[6]. It is recommended to conduct genotyping of Rotavirus on large samples before starting vaccination in the country.
机译:背景技术轮状病毒是世界各地婴儿和幼儿中腹泻的主要原因,导致每年有超过500,000人死亡和240万住院治疗。在尼泊尔轮状病毒患者的情况下,阳性率范围从17.0至39.0%少于5岁的孩子。然而,关于RotaVirus的分子基因型众所周知。本研究的目的是估算轮状病毒胃肠炎的负担,并确定少于5年的儿童轮状病毒的基因型。方法采用跨剖面研究于2014年1月至11月,儿童少于5岁,前往Kanti儿童医院和培训大学教学医院。使用前景轮状病毒微孔板测定法通过酶联免疫吸附测定(ELISA)进行轮状病毒抗原检测。在轮状病毒抗原阳性样品中,59个样品用于轮状病毒RNA提取。进行多重PCR以鉴定包含G1-G4,G8-G10和G12和P型包含P [4],P [6],P [8],P [9],P [10]和P [ 11]。结果总共收集了717个腹泻粪便样品,从10个月到59岁以下的患者收集。在(n =β164)22.9%的患者中发现了Rotavirus抗原阳性。 1月份的腹泻数量最多。 RotaVirus基因型的分子分析显示,主要的G型为G12(36%),然后是G9(31%),G1(21%),G2(8.6%)。 P6(32.8%),P8(31%),P10(14.8%),P4(14.8%)。鉴定了总共七个G / P型组合是G12P [6](35.8%),G1P [8](15.1%),G9P [8](15.1%)。结论RotaVirus腹泻是,大多数影响7至24个月的儿童在尼泊尔,主要发生在冬季。发现该国的循环基因型主要是G12P的主要基因型和优势[6]。建议在该国开始疫苗接种之前对大型样品进行RotaVirus的基因分型。

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