首页> 外文期刊>American Journal of Infectious Diseases and Microbiology >Detection and Molecular Characterization of Respiratory Syncytial Virus (RSV) in Children with Respiratory Signs in Khartoum State, Sudan 2011-2012
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Detection and Molecular Characterization of Respiratory Syncytial Virus (RSV) in Children with Respiratory Signs in Khartoum State, Sudan 2011-2012

机译:2011-2012年苏丹喀土穆州有呼吸道症状的儿童呼吸道合胞病毒(RSV)的检测和分子表征

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Background: The present study was to investigate the incidence of the respiratory syncytial virus infection in children and to characterize the RSV circulating in Khartoum state during 2011-12 winter seasons. Methodology: Throat swab specimens collected from 224 children less than 5 years old, with respiratory tract infections admitted at Khartoum Hospitals in winter season (2011- 2012), were screened for RSV using direct immunofluorescence assay (DFA) and reverse transcription- polymerase chain reaction (RT-). Isolation in cell culture followed by nucleotide sequencing and bioinformatics analysis based on the G gene, were done for the RT- positive RSV samples. Results: Out of 224 patients, RSV infections were detected in 136 (60.7%) patients, by using DFA technique, and 44 (19.6%) patients using RT-PCR. 22 strains of RSV were isolated in Hep-2 cell line. The clinical symptoms including Bronchiolitis, Pneumonia, Asthma and Allergy showed significantly different rates (p<0.05) in having RSV infection, (P-value = 0.017, 0.002, 0.0001, 0.0001) respectively. Bioinformatics analysis of nucleotide sequences of 7 cell culture isolated RSV strains revealed that all analyzed RSV belonged to the RSV-A genotype. Phylogenetic tree of RSV-A sequences showed that, all Sudanese strains were grouped with strains from Belgium and Saudi Arabia. Conclusions: This is the first report on molecular characterization that describes the circulation of RSV genotype in Sudan. DFA and RT-PCR offers rapid methods for detection of RSV in hospitalized children with Respiratory tract infection (RTI).
机译:背景:本研究旨在调查儿童呼吸道合胞病毒感染的发生率,并分析2011-12冬季喀土穆州的RSV传播情况。方法:采用直接免疫荧光法(DFA)和逆转录-聚合酶链反应,从喀土穆医院在冬季(2011-2012年)收治的224例小于5岁的儿童的呼吸道拭子样本中检测RSV。 (RT-)。对RT阳性RSV样品进行细胞培养分离,然后进行核苷酸测序和基于G基因的生物信息学分析。结果:在224例患者中,通过DFA技术检测出136例(60.7%)患者的RSV感染,通过RT-PCR检测到44例(19.6%)的RSV感染。在Hep-2细胞系中分离出22株RSV。包括毛细支气管炎,肺炎,哮喘和过敏在内的临床症状显示RSV感染的发生率显着不同(p <0.05)(P值分别为0.017、0.002、0.0001、0.0001)。对7种细胞培养分离的RSV毒株核苷酸序列的生物信息学分析表明,所有分析的RSV均属于RSV-A基因型。 RSV-A序列的系统进化树表明,所有苏丹菌株均与比利时和沙特阿拉伯的菌株分组。结论:这是描述苏丹RSV基因型循环的分子表征的第一份报告。 DFA和RT-PCR为住院呼吸道感染(RTI)的儿童提供了快速检测RSV的方法。

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