在引入轮状病毒疫苗接种10年后,刚果5岁以下儿童因肠胃炎住院的轮状病毒感染率

IF 1.5 Q4 INFECTIOUS DISEASES
Cedeche Lebraiche Durain Mboungou , Claujens Chastel Mfoutou Mapanguy , Alain Maxime Mouanga , Vivaldie Mikounou Louya , Jeannhey Christevy Vouvoungui , Raoul Ampa , Francine Ntoumi
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引用次数: 0

摘要

目的轮状病毒A (RVA)仍然是急性严重胃肠炎的主要病因,在世界范围内与儿童住院率和死亡率高相关。在低收入国家,RVA感染的流行程度各不相同。此外,其遗传多样性可能因地区而异,并可能影响其流行程度。为了控制刚果共和国流行的RVA新毒株的出现,必须了解G和P基因型的多样性,这可能会降低疫苗的有效性。因此,本研究旨在确定住院儿童中RVA菌株的患病率和基因型多样性,无论是否接种疫苗。此外,还确定了疾病严重程度的潜在危险因素。方法研究时间为2022年4月~ 2023年3月。收集儿科病房急性胃肠炎住院的5岁以下儿童的粪便样本,并使用商用酶联免疫吸附试验(ELISA)检测RVA病例。同时,多重逆转录聚合链反应(RT-PCR)用于RVA检测和基因分型。所有多重RT-PCR结果不明确的样品都进行测序。结果共纳入227例住院儿童进行RVA感染检测。ELISA和PCR检测分别有59例(26%)和131例(57.7%)感染RVA。所有ELISA检测结果阳性的个体均经PCR证实为rva阳性。在98名有记录的RVA疫苗接种史的儿童中,60%出现RVA感染。24小时内出现三次以上呕吐以及接种疫苗和采集样本之间的时间与RVA感染有关。RVA基因分型显示6种P型(P[4];P [6];P [8];P [9];P [10];和P[11])。优势基因型为(P bb0 15.3%;P [6] 13.7%;P [8] 22.1%;P[9] 14.5%)。在8种G型中,G3(13.7%)、G4(12.2%)、G1(6.9%)最为常见。没有特定的基因型分布作为疫苗接种史的功能。结论:与实施轮状病毒疫苗接种前的研究结果相比,在本报告中,我们观察到住院儿童RVA感染率下降了约20%。结果表明,在布拉柴维尔,刚果共和国至少进行了10年的轮状病毒疫苗接种,取得了显著效果,尽管据报道,在中低收入国家疫苗的效力有所下降。因此,研究结果支持加强努力,通过国家疫苗接种规划提高覆盖率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The prevalence of rotavirus infection among Congolese children younger than 5 years hospitalized for gastroenteritis 10 years after introduction of rotavirus vaccination

Objectives

Rotavirus A (RVA) remains the primary cause of acute severe gastroenteritis associated with high rates of childhood hospitalization and mortality worldwide. The prevalence of RVA infection varies within low-income countries. In addition, its genetic diversity may vary among regions and may affect its prevalence. To control the emergence of new strains of RVA circulating in the Republic of Congo, it is essential to know the diversity of both G and P genotypes, which could render the vaccine less effective. Therefore, this study aimed to determine the prevalence and genotype diversity of RVA strains in children who were hospitalized, whether vaccinated or not. Moreover, the potential risk factors of disease severity are identified.

Methods

The study was conducted from April 2022 to March 2023. Stool samples were collected from children younger than 5 years, hospitalized in a pediatric ward for acute gastroenteritis, and a commercial enzyme-linked immunosorbent assay (ELISA) was used to detect RVA cases. In parallel, a multiplex reverse transcription-polymerization chain reaction (RT-PCR) was performed for RVA detection and genotyping. All samples with ambiguous multiplex RT-PCR results were subjected to sequencing.

Results

A total of 227 children hospitalized were enrolled and tested for RVA infection. Using ELISA and PCR, 59 (26%) and 131 (57.7%) individuals were found to be infected with RVA, respectively. All individuals with a positive ELISA test result were confirmed as RVA-positive by PCR. Of the 98 children with documented histories of RVA vaccination, 60% presented with RVA infection. The occurrence of vomiting on more than three occasions within a 24-hour period and the time between vaccination and sample collection were found to be associated with RVA infection. RVA genotyping revealed six P types (P[4]; P[6]; P[8]; P[9]; P[10]; and P[11]). The predominant genotypes were (P[4] 15.3%; P[6] 13.7%; P[8] 22.1%; P[9] 14.5%). Among the eight G types, the most prevalent were G3 (13.7%), G4 (12.2%), and G1 (6.9%). No specific genotype distribution was discernible as a function of vaccination history.

Conclusions

Compared with the findings of our study before the implementation of rotavirus vaccination, in this report, we observed a roughly 20% decreased prevalence of RVA infection in children hospitalized. The results suggest that in Brazzaville at least, 10 years of rotavirus vaccination in the Republic of Congo have had a substantial effect, despite the reported reduced efficacy of the vaccines in low- and middle-income countries. The findings thus support enhanced efforts to increase coverage through national vaccination programs.
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IJID regions
IJID regions Infectious Diseases
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