%0 Journal Article %T Enterovirus detection in different regions of Madagascar reveals a higher abundance of enteroviruses of species C in areas where several outbreaks of vaccine-derived polioviruses occurred %+ Institut Pasteur de Madagascar %+ Signalisation antivirale - Virus sensing and signaling %+ Direction Internationale de l'Institut Pasteur %+ Institut Pasteur [Paris] (IP) %A Razafindratsimandresy, Richter %A Joffret, Marie-Line %A Andriamandimby, Soa Fy %A Andriamamonjy, Seta %A Rabemanantsoa, Sendraharimanana %A Richard, Vincent %A Delpeyroux, Francis %A Heraud, Jean-Michel %A Bessaud, Maël %Z Stools specimens analyzed in the current study were obtained thanks to the financial support provided by the Agence inter-établissement de Recherche pour le Développement (IRD) in Madagascar, the Agence Nationale de la Recherche (ANR) (Grant#ANR-09-MIEN-019) and the Fondation pour la Recherche Médicale (FRM) (Grant#DMI20091117313) in France. %< avec comité de lecture %@ 1471-2334 %J BMC Infectious Diseases %I BioMed Central %V 22 %N 1 %P 821 %8 2022-11 %D 2022 %R 10.1186/s12879-022-07826-0 %M 36348312 %Z Life Sciences [q-bio] %Z Life Sciences [q-bio]/Microbiology and Parasitology/VirologyJournal articles %X Abstract Background Poliomyelitis outbreaks due to pathogenic vaccine-derived polioviruses (VDPVs) are threatening and complicating the global polio eradication initiative. Most of these VDPVs are genetic recombinants with non-polio enteroviruses (NPEVs) of species C. Little is known about factors favoring this genetic macroevolution process. Since 2001, Madagascar has experienced several outbreaks of poliomyelitis due to VDPVs, and most of VDPVs were isolated in the south of the island. The current study explored some of the viral factors that can promote and explain the emergence of recombinant VDPVs in Madagascar. Methods Between May to August 2011, we collected stools from healthy children living in two southern and two northern regions of Madagascar. Virus isolation was done in RD, HEp-2c, and L20B cell lines, and enteroviruses were detected using a wide-spectrum 5ʹ-untranslated region RT-PCR assay. NPEVs were then sequenced for the VP1 gene used for viral genotyping. Results Overall, we collected 1309 stools, of which 351 NPEVs (26.8%) were identified. Sequencing revealed 33 types of viruses belonging to three different species: Enterovirus A (8.5%), Enterovirus B (EV-B, 40.2%), and Enterovirus C (EV-C, 51.3%). EV-C species included coxsackievirus A13, A17, and A20 previously described as putative recombination partners for poliovirus vaccine strains. Interestingly, the isolation rate was higher among stools originating from the South (30.3% vs. 23.6%, p-value = 0.009). EV-C were predominant in southern sites (65.7%) while EV-B predominated in northern sites (54.9%). The factors that explain the relative abundance of EV-C in the South are still unknown. Conclusions Whatever its causes, the relative abundance of EV-C in the South of Madagascar may have promoted the infections of children by EV-C, including the PV vaccine strains, and have favored the recombination events between PVs and NPEVs in co-infected children, thus leading to the recurrent emergence of recombinant VDPVs in this region of Madagascar. %G English %2 https://pasteur.hal.science/pasteur-04103923/document %2 https://pasteur.hal.science/pasteur-04103923/file/s12879-022-07826-0.pdf %L pasteur-04103923 %U https://pasteur.hal.science/pasteur-04103923 %~ PASTEUR %~ RIIP %~ CNRS %~ RIIP_MADAGASCAR %~ UNIV-PARIS %~ UNIVERSITE-PARIS %~ ANR %~ FRM %~ VIR-SENS %~ PASTEUR_UMR3569