Mboungou Cedeche Lebraiche Durain, Mfoutou Mapanguy Claujens Chastel, Mouanga Alain Maxime, Mikounou Louya Vivaldie, Vouvoungui Jeannhey Christevy, Ampa Raoul, Ntoumi Francine
Fondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Faculty of Sciences and Techniques, Marien Ngouabi University, Brazzaville, Republic of Congo.
IJID Reg. 2025 Feb 13;14:100596. doi: 10.1016/j.ijregi.2025.100596. eCollection 2025 Mar.
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.
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.
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.
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.
A组轮状病毒(RVA)仍然是全球范围内导致急性重症胃肠炎的主要原因,与儿童住院率和死亡率居高不下相关。RVA感染在低收入国家的流行情况各不相同。此外,其基因多样性在不同地区可能存在差异,并可能影响其流行程度。为了控制刚果共和国境内新出现的RVA毒株的传播,了解G和P基因型的多样性至关重要,因为这可能会使疫苗效果降低。因此,本研究旨在确定住院儿童(无论是否接种过疫苗)中RVA毒株的流行情况和基因型多样性。此外,还确定了疾病严重程度的潜在风险因素。
本研究于2022年4月至2023年3月进行。收集了5岁以下因急性胃肠炎入住儿科病房的儿童的粪便样本,并使用商业酶联免疫吸附测定(ELISA)检测RVA病例。同时,进行多重逆转录聚合酶链反应(RT-PCR)以检测RVA并进行基因分型。所有多重RT-PCR结果不明确的样本均进行测序。
共有227名住院儿童参与了RVA感染检测。使用ELISA和PCR检测,分别发现59名(26%)和131名(57.7%)个体感染了RVA。所有ELISA检测结果呈阳性的个体均通过PCR确认为RVA阳性。在98名有RVA疫苗接种记录的儿童中,60%出现了RVA感染。发现24小时内呕吐超过三次以及接种疫苗与样本采集之间的时间与RVA感染有关。RVA基因分型显示有六种P型(P[4];P[6];P[8];P[9];P[10];和P[11])。主要基因型为(P[4] 15.3%;P[6] 13.7%;P[8] 22.1%;P[9] 14.5%)。在八种G型中,最常见的是G3(13.7%)、G4(12.2%)和G1(6.9%)。未发现与疫苗接种史相关的特定基因型分布。
与我们在实施轮状病毒疫苗接种之前的研究结果相比,在本报告中,我们观察到住院儿童中RVA感染的流行率下降了约20%。结果表明,至少在布拉柴维尔,刚果共和国10年的轮状病毒疫苗接种产生了显著效果,尽管有报道称该疫苗在低收入和中等收入国家的效力有所降低。因此,这些发现支持通过国家疫苗接种计划加大覆盖力度的努力。