Kiulia N M, Peenze I, Dewar J, Nyachieo A, Galo M, Omolo E, Steele A D, Mwenda J M
Institute of Primate Research, P.O. Box 24481-00502, Karen, Nairobi, Kenya.
East Afr Med J. 2006 Jul;83(7):360-5. doi: 10.4314/eamj.v83i7.9447.
Rotavirus is the most common cause of severe infantile diarrhoea disease in infants and young children below five years worldwide. Rotavirus is associated with high cases of morbidity and mortality and it is estimated that up to 650,000 deaths in young children occur annually in the less developed countries and approximately 150,000-200,000 deaths occur in Africa alone.
To characterise the circulating rotavirus strains in Maua, Meru North district, Kenya.
A prospective study to investigate and characterise rotavirus serotypes/genotypes and electropherotypes in infants and children with severe diarrhoea hospitalised and/or attending the outpatient department of Maua Methodist Hospital during the period April 2004 to September 2005.
Maua Methodist Hospital, Meru North, Kenya.
Faecal samples were collected from 135 infants and children with acute diarrhoea and were screened first for the presence of human Group A rotavirus antigen using commercially available enzyme linked immunosorbent assay kit (ELISA). The positive samples were evaluated by sodium dodecyl polycrylamide gel electrophoresis (SDS-PAGE) to determine the viral RNA electropherotype profile. Rotavirus strains were also genotyped using reverse transcriptase polymerase chain reaction (RT-PCR) of the VP7 gene.
Assay of these samples with commercial ELISA showed that 17.8% (24/135) were positive for group A rotavirus antigen. Twenty of these ELISA positive samples were also analysed by SDS-PAGE of which 75% (15/20) gave detectable electropherotype pattern with the long electropherotype being predominant 80.0% (12/15) followed by the short RNA profile 20.0% (2/ 15). Seventeen of the ELISA positive samples were genotyped for VP7 and the results showed that G9 was the most predominant genotype comprising 47.1% (8/17) followed by G8 29.4% (5/17), GI 17.4% (3/17) and the mixed genotype was G8/G9 5.9% (1/17). Most patients with rotavirus infection were of the age of 3 - 60 months, with 79% being less than 18 months old.
The overall prevalence of rotavirus infection in young children with diarrhoea hospitalised and/or attending the out-patient department of Maua Methodist Hospital was 17.8% with the predominant serotype being G9. These results show that rotavirus plays an important role in severe viral diarrhoea in young children in Maua Meru North district, Kenya. Furthermore, this high G9 rotavirus prevalence in Kenya may require vaccine trials to be held in Kenya so as to determine the efficacy of new rotavirus vaccine candidates that do not include the G9 serotype.
轮状病毒是全球五岁以下婴幼儿严重腹泻疾病的最常见病因。轮状病毒与高发病率和高死亡率相关,据估计,在欠发达国家,每年有多达65万幼儿死亡,仅在非洲就有大约15万至20万例死亡。
对肯尼亚梅鲁北区马乌阿市流行的轮状病毒株进行特征分析。
一项前瞻性研究,旨在调查和分析2004年4月至2005年9月期间在马乌阿卫理公会医院住院和/或门诊就诊的重症腹泻婴幼儿的轮状病毒血清型/基因型和电泳图谱型。
肯尼亚梅鲁北区马乌阿卫理公会医院。
从135名急性腹泻婴幼儿中采集粪便样本,首先使用市售酶联免疫吸附测定试剂盒(ELISA)筛查人A组轮状病毒抗原的存在情况。对阳性样本进行十二烷基聚丙烯酰胺凝胶电泳(SDS-PAGE)评估,以确定病毒RNA电泳图谱型。还使用VP7基因的逆转录聚合酶链反应(RT-PCR)对轮状病毒株进行基因分型。
用商业ELISA检测这些样本显示,17.8%(24/135)的样本A组轮状病毒抗原呈阳性。对其中20份ELISA阳性样本也进行了SDS-PAGE分析,其中75%(15/20)呈现出可检测的电泳图谱型,长电泳图谱型占主导地位,为80.0%(12/15),短RNA图谱型占20.0%(2/15)。对17份ELISA阳性样本进行VP7基因分型,结果显示G9是最主要的基因型,占47.1%(8/17),其次是G8,占29.4%(5/17),G1占17.4%(3/17),混合基因型为G8/G9,占5.9%(1/17)。大多数轮状病毒感染患者年龄在3至60个月之间,79%小于18个月。
在马乌阿卫理公会医院住院和/或门诊就诊的腹泻幼儿中,轮状病毒感染的总体患病率为17.8%,主要血清型为G9。这些结果表明,轮状病毒在肯尼亚梅鲁北区马乌阿市幼儿严重病毒性腹泻中起重要作用。此外,肯尼亚这种高比例的G9轮状病毒流行情况可能需要在肯尼亚进行疫苗试验,以确定不包含G9血清型的新型轮状病毒候选疫苗的疗效。