Faculdade de Medicine, Universidade Agostinho Neto, Luanda, Angola.
CISA-Centro de Investigação em Saúde de Angola, Caxito, Bengo, Angola.
Viruses. 2024 Feb 3;16(2):243. doi: 10.3390/v16020243.
Human type A rotavirus (RV-A) is world-recognized as the major pathogen causing viral gastroenteritis in children under 5 years of age. The literature indicates a substantial increase in the diversity of rotavirus strains across continents, especially in Africa, which can pose significant challenges including an increase of disease burden and a reduction of vaccines' effectiveness. However, few studies have mapped the variety of circulating virus strains in different regions, which may hamper decisions on epidemiological surveillance and preventive public health measures. Thus, our aim was to compile the most updated available evidence on the genetic profile of RV-A among children in Africa and determine the prevalence of different genotypes according to the geographical regions by means of a broad systematic review. Systematic searches were performed in PubMed, Scopus, Web of Science, and Scielo without language, time limits, or geographical restrictions within the African continent. We selected full-text peer-reviewed articles assessing the genetic profile (i.e., genotyping) of RV-A in children up to 5 years old in Africa. Overall, 682 records were retrieved, resulting in 75 studies included for evidence synthesis. These studies were published between 1999 and 2022, were conducted in 28 countries from the five African regions, and 48% of the studies were carried out for 24 months or more. Most studies (n = 55; 73.3%) evaluated RV-A cases before the introduction of the vaccines, while around 20% of studies (n = 13) presented data after the vaccine approval in each country. Only seven (9.3%) studies compared evidence from both periods (pre- and post-vaccine introduction). Genotyping methods to assess RV-A varied between RT-PCR, nested or multiplex RT-PCR, testing only the most common P and G-types. We observed G1 and P[8] to be the most prevalent strains in Africa, with values around 31% and 43%, respectively. Yet if all the genotypes with the following highest prevalence were added ((G1 + G2, G3, G9) and (P[8] + P[6], P[4])), these figures would represent 80% and 99% of the total prevalence. The combination G1P[8] was the most reported in the studies (around 22%). This review study demonstrated an increased strain diversity in the past two decades, which could represent a challenge to the efficacy of the current vaccine.
人源 A 型轮状病毒(RV-A)是公认的导致 5 岁以下儿童病毒性肠胃炎的主要病原体。文献表明,轮状病毒株在各大洲的多样性显著增加,尤其是在非洲,这可能带来重大挑战,包括疾病负担增加和疫苗效力降低。然而,很少有研究针对不同地区循环病毒株的多样性进行绘图,这可能会阻碍流行病学监测和预防公共卫生措施的决策。因此,我们的目的是汇总非洲儿童中 RV-A 的最新遗传特征证据,并通过广泛的系统综述,根据地理位置确定不同基因型的流行率。在非洲大陆内,我们在 PubMed、Scopus、Web of Science 和 Scielo 中进行了系统搜索,没有语言、时间限制或地理限制。我们选择了评估非洲儿童中 RV-A 遗传特征(即基因分型)的全文同行评审文章。总体而言,共检索到 682 条记录,最终纳入了 75 项研究进行证据综合。这些研究发表于 1999 年至 2022 年,在非洲的 28 个国家进行,其中 48%的研究持续 24 个月或更长时间。大多数研究(n = 55;73.3%)评估了疫苗接种前的 RV-A 病例,而大约 20%的研究(n = 13)在每个国家批准疫苗后提供了数据。只有 7 项(9.3%)研究比较了疫苗接种前后(接种前和接种后)的证据。评估 RV-A 的基因分型方法在 RT-PCR、巢式或多重 RT-PCR 之间有所不同,仅检测最常见的 P 和 G 型。我们观察到 G1 和 P[8]是非洲最流行的株,分别约为 31%和 43%。然而,如果将以下具有最高流行率的所有基因型((G1+G2、G3、G9)和(P[8]+P[6]、P[4]))相加,这些数字将分别代表总流行率的 80%和 99%。在研究中报告最多的是组合 G1P[8](约 22%)。本综述研究表明,在过去二十年中,株的多样性有所增加,这可能对当前疫苗的效力构成挑战。