Putnam Shannon D, Sedyaningsih Endang R, Listiyaningsih Erlin, Pulungsih Sri Pandam, Soenarto Yati, Salim Octavianus Ch, Subekti Decy, Riddle Mark S, Burgess Timothy H, Blair Patrick J
U.S. Naval Medical Research Unit No. 2, Jakarta, Indonesia.
J Clin Virol. 2007 Dec;40(4):289-94. doi: 10.1016/j.jcv.2007.09.005. Epub 2007 Oct 30.
Globally, group A rotavirus causes significant morbidity and mortality among children. Limited data exist on the epidemiology of rotavirus disease among Indonesian children.
We describe the epidemiology of rotavirus-associated diarrhea among Indonesian children <6 years of age, including clinical symptoms and genotypes.
We conducted a hospital-based, case series study at four referral hospitals between February 2004 and February 2005 among children with diarrhea. Rotavirus positivity was defined by a positive result from either EIA or RT-PCR. A semi-nested RT-PCR was used to determine specific rotavirus genotypes.
1660 stools were tested for pathogens. The overall rotavirus prevalence was 45.5%. Children with rotavirus-associated diarrhea were significantly younger (p<0.0001) and more likely to be hospitalized (81.3% versus 72.2%; p<0.0001). Symptoms associated with rotavirus included, vomiting, fever, nausea, fatigue and dehydration, while bloody stool was significantly less common with rotavirus-associated diarrhea.
Rotavirus was an important contributor of morbidity to our study sample. Rotavirus genotyping demonstrated a temporal shift from G1-G4 to G9, but this was highly associated with the P[8] gene, suggesting that a multivalent rotavirus vaccine, incorporating G9 P[8] antigen, may reduce the burden of diarrheal illnesses among Indonesian children.
在全球范围内,A组轮状病毒导致儿童出现严重的发病和死亡情况。关于印度尼西亚儿童轮状病毒病流行病学的数据有限。
我们描述了印度尼西亚6岁以下儿童轮状病毒相关性腹泻的流行病学情况,包括临床症状和基因型。
2004年2月至2005年2月期间,我们在四家转诊医院对腹泻儿童进行了一项基于医院的病例系列研究。轮状病毒阳性定义为酶免疫分析(EIA)或逆转录聚合酶链反应(RT-PCR)结果呈阳性。采用半巢式RT-PCR确定特定的轮状病毒基因型。
对1660份粪便进行了病原体检测。轮状病毒总体患病率为45.5%。轮状病毒相关性腹泻患儿明显更年幼(p<0.0001),且住院可能性更高(81.3%对72.2%;p<0.0001)。与轮状病毒相关的症状包括呕吐、发热、恶心、疲劳和脱水,而血性便在轮状病毒相关性腹泻中明显较少见。
轮状病毒是我们研究样本中发病的一个重要因素。轮状病毒基因分型显示从G1-G4到G9的时间变化,但这与P[8]基因高度相关,这表明包含G9 P[8]抗原的多价轮状病毒疫苗可能减轻印度尼西亚儿童腹泻疾病的负担。