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Molecular Epidemiology and Clinical Features of Rotavirus Infection Among Pediatric Patients in East Java Indonesia During 2015–2018: Dynamic Changes in Rotavirus Genotypes From Equine-Like G3 to Typical Human G1/G3

机译:印度尼西亚东爪哇省儿科患者轮状病毒感染的分子流行病学和临床特征(2015-2018年):轮状病毒基因型从马似G3到典型人类G1 / G3的动态变化

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摘要

Group A rotavirus (RVA) is the most important cause of severe gastroenteritis among children worldwide, and effective RVA vaccines have been introduced in many countries. Here we performed a molecular epidemiological analysis of RVA infection among pediatric patients in East Java, Indonesia, during 2015–2018. A total of 432 stool samples were collected from hospitalized pediatric patients with acute gastroenteritis. None of the patients in this cohort had been immunized with an RVA vaccine. The overall prevalence of RVA infection was 31.7% (137/432), and RVA infection was significantly more prevalent in the 6- to 11-month age group than in the other age groups (P < 0.05). Multiplex reverse transcription-PCR (RT-PCR) revealed that the most common G-P combination was equine-like G3P[8] (70.8%), followed by equine-like G3P[6] (12.4%), human G1P[8] (8.8%), G3P[6] (1.5%), and G1P[6] (0.7%). Interestingly, the equine-like strains were exclusively detected until May 2017, but in July 2017 they were completely replaced by a typical human genotype (G1 and G3), suggesting that the dynamic changes in RVA genotypes from equine-like G3 to typical human G1/G3 in Indonesia can occur even in the country with low RVA vaccine coverage rate. The mechanism of the dynamic changes in RVA genotypes needs to be explored. Infants and children with RVA-associated gastroenteritis presented more frequently with some dehydration, vomiting, and watery diarrhea, indicating a greater severity of RVA infection compared to those with non-RVA gastroenteritis. In conclusion, a dynamic change was found in the RVA genotype from equine-like G3 to a typical human genotype. Since severe cases of RVA infection were prevalent, especially in children aged 6 to 11 months or more generally in those less than 2 years old, RVA vaccination should be included in Indonesia’s national immunization program.
机译:A组轮状病毒(RVA)是全世界儿童严重肠胃炎的最重要原因,许多国家已经引入有效的RVA疫苗。在这里,我们对2015-2018年印度尼西亚东爪哇省的小儿患者的RVA感染进行了分子流行病学分析。从住院的急性胃肠炎小儿患者中收集了总共432份粪便样本。该队列中没有患者接受RVA疫苗免疫。 RVA感染的总体患病率为31.7%(137/432),在6至11个月年龄组中RVA感染的发生率明显高于其他年龄组(P <0.05)。多重逆转录PCR(RT-PCR)显示,最常见的GP组合是马类G3P [8](70.8%),其次是马类G3P [6](12.4%)人G1P [8]( 8.8%),G3P [6](1.5%)和G1P [6](0.7%)。有趣的是,直到2017年5月才专门检测到马类病毒株,但在2017年7月,它们被典型的人类基因型(G1和G3)完全取代,表明RVA基因型从马类G3到典型的人类G1的动态变化即使在RVA疫苗覆盖率较低的国家,印度尼西亚也可能出现/ G3。 RVA基因型动态变化的机制需要探索。患有RVA相关性肠胃炎的婴儿和儿童出现脱水,呕吐和水样腹泻的频率更高,这表明与非RVA胃肠炎相比,RVA感染的严重性更高。总之,在RVA基因型中发现了动态变化,从马样G3到典型的人类基因型。由于RVA感染的严重病例很普遍,尤其是在6至11个月或更广泛的2岁以下儿童中,因此RVA疫苗接种应纳入印度尼西亚的国家免疫计划。

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