Bosch Albert, Carcereny Albert, García-Pedemonte David, Fuentes Cristina, Costafreda Maria I, Pintó Rosa M, Guix Susana
Department of Genetics, Microbiology and Statistics, School of Biology, Enteric Virus Laboratory, Barcelona 08028, Spain.
INSA, 2 Support for Virus Analysis in the Food Chain and the Water Cycle, Institute of Nutrition and Food Safety, University of Barcelona, Santa Coloma de Gramenet, Barcelona 08921, Spain.
J Appl Microbiol. 2025 Jan 6;136(1). doi: 10.1093/jambio/lxae311.
Enteroviruses (EVs) are a highly diverse group of viruses multiplying primarily in the gastrointestinal tract and/or the upper respiratory tract, initially distributed in two separate genera: Enterovirus and Rhinovirus, respectively. According to the similarities in genome organization and particle structure, rhinovirus species were later reclassified as also belonging to genus Enterovirus. Human EV infections are usually asymptomatic or causing mild clinical manifestations. Nevertheless, some EV infections may derive in severe neural complications, including acute flaccid paralysis (AFP) such as poliomyelitis, whose etiological agent is poliovirus, a member of the Enterovirus C species. The inactivated polio vaccine (IPV) and particularly the oral attenuated polio vaccine (OPV) have contributed to the virtual eradication of the disease. However, sustained global circulation of vaccine-derived poliovirus 2 (cVDPV2), originated from the genetic instability of OPV strain 2 and intertypic recombination between Sabin OPV strains and members of the Enterovirus C species, still causes outbreaks of AFP worldwide. In addition, humanitarian crises, in particular armed conflicts, hamper polio vaccination campaigns and facilitate the occurrence of cases. Additionally, besides poliovirus, other EV may also cause AFP, among them EV A71 or EV D68, and it is highly advisable to implement wastewater surveillance to elucidate the occurrence of not only polioviruses, but also of other EV susceptible to derive in serious neural complications, since the screening of viral RNA in cerebrospinal fluid samples in patients suffering from AFP is not a reliable diagnostic tool.
肠道病毒(EVs)是一类高度多样化的病毒,主要在胃肠道和/或上呼吸道中增殖,最初分别分布在两个不同的属:肠道病毒属和鼻病毒属。根据基因组组织和颗粒结构的相似性,鼻病毒种后来被重新分类为也属于肠道病毒属。人类EV感染通常无症状或引起轻微的临床表现。然而,一些EV感染可能导致严重的神经并发症,包括急性弛缓性麻痹(AFP),如脊髓灰质炎,其病原体是脊髓灰质炎病毒,属于肠道病毒C种的成员。灭活脊髓灰质炎疫苗(IPV),特别是口服减毒脊髓灰质炎疫苗(OPV),为该疾病的实际根除做出了贡献。然而,源自OPV 2株的基因不稳定性以及Sabin OPV株与肠道病毒C种成员之间的型间重组导致的疫苗衍生脊髓灰质炎病毒2(cVDPV2)在全球的持续传播,仍然在全球范围内引发AFP疫情。此外,人道主义危机,特别是武装冲突,阻碍了脊髓灰质炎疫苗接种运动并助长了病例的发生。此外,除了脊髓灰质炎病毒外,其他EV也可能导致AFP,其中包括EV A71或EV D68,并且非常有必要开展废水监测,以阐明不仅脊髓灰质炎病毒,而且其他易引发严重神经并发症的EV的发生情况,因为对AFP患者脑脊液样本中的病毒RNA进行筛查并不是一种可靠的诊断工具。