Hellferscee Orienka, Tempia Stefano, Walaza Sibongile, Variava Ebrahim, Dawood Halima, Wolter Nicole, Madhi Shabir A, du Plessis Mignon, Cohen Cheryl, Treurnicht Florette K
National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
University of the Witwatersrand, Johannesburg, South Africa.
J Med Virol. 2017 Oct;89(10):1759-1767. doi: 10.1002/jmv.24869. Epub 2017 Jul 6.
Enteroviruses can cause outbreaks of severe acute respiratory illness (SARI) and EV-A, -B, -C, and -D species have different pathogenic profiles and circulation patterns. We aimed to characterize and determine the prevalence of enterovirus genotypes among South African patients with respiratory illness and controls during June 2012 to July 2014. Syndromic SARI and influenza-like illness (ILI) surveillance was performed at two sentinel sites. At each site nasopharyngeal/oropharyngeal specimens were collected from SARI and ILI patients as well as controls. Specimens were tested for enterovirus by real-time PCR. Positive specimens were further genotyped by sequencing a region of the VP1 gene. The prevalence of enterovirus was 5.8% (87/1494), 3.4% (103/3079), and 3.4% (46/1367) among SARI, ILI, and controls, respectively (SARI/controls, P = 0.002 and ILI/control, P = 0.973). Among the 101/236 (42.8%) enterovirus-positive specimens that could be genotyped, we observed a high diversity of circulating enterovirus genotypes (a total of 33 genotypes) from all four human enterovirus species with high prevalence of Enterovirus-B (60.4%; 61/101) and Enterovirus-A (21.8%; 22/101) compared to Enterovirus-C (10.9%; 11/101) and Enterovirus-D (6.9%; 7/101) (P = 0.477). Of the enterovirus genotypes identified, Echovirus 30 (9.9%, 10/101), Coxsackie virus B5 (7.9%, 8/101) and Enterovirus-D68 (6.9%, 7/101) were most prevalent. There was no difference in disease severity (SARI or ILI compared to controls) between the different enterovirus species (P = 0.167). We observed a high number of enterovirus genotypes in patients with respiratory illness and in controls from South Africa with no disease association of EV species with disease severity.
肠道病毒可引发严重急性呼吸道疾病(SARI)的暴发,且肠道病毒A、B、C和D型具有不同的致病特征和传播模式。我们旨在对2012年6月至2014年7月期间南非呼吸道疾病患者及对照人群中的肠道病毒基因型进行特征分析并确定其流行率。在两个哨点开展了症状性SARI和流感样疾病(ILI)监测。在每个哨点,采集了SARI和ILI患者以及对照人群的鼻咽/口咽标本。通过实时PCR检测标本中的肠道病毒。对阳性标本进一步通过对VP1基因区域进行测序来进行基因分型。肠道病毒在SARI、ILI和对照人群中的流行率分别为5.8%(87/1494)、3.4%(103/3079)和3.4%(46/1367)(SARI/对照,P = 0.002;ILI/对照,P = 0.973)。在236份可进行基因分型的标本中有101份(42.8%)肠道病毒阳性,我们观察到来自所有四种人类肠道病毒型别的循环肠道病毒基因型具有高度多样性(共33种基因型),其中肠道病毒B型(60.4%;61/101)和肠道病毒A型(21.8%;22/101)的流行率高于肠道病毒C型(10.9%;11/101)和肠道病毒D型(6.9%;7/101)(P = 0.477)。在鉴定出的肠道病毒基因型中,埃可病毒30型(9.9%,10/101)、柯萨奇病毒B5型(7.9%,8/101)和肠道病毒D68型(6.9%,7/101)最为常见。不同肠道病毒型别之间在疾病严重程度方面(与对照相比的SARI或ILI)没有差异(P = 0.167)。我们在南非的呼吸道疾病患者及对照人群中观察到大量肠道病毒基因型,且肠道病毒型别与疾病严重程度之间无疾病关联。