Detection of ON1 and novel genotypes of human respiratory syncytial virus and emergence of palivizumab resistance in Lebanon

Abstract

Respiratory syncytial virus (RSV) is a common cause of respiratory tract infections in children and immunocompromised individuals. A multi-center surveillance of the epidemiologic and molecular characteristics of RSV circulating in Lebanon was performed. The attachment (G) and fusion (F) glycoproteins were analyzed and compared to those reported regionally and globally. 16% (83/519) of the nasopharyngeal swabs collected during the 2016/17 season tested positive for RSV; 50% (27/54) were RSV-A and 50% (27/54) were RSV-B. Phylogenetic analysis of the G glycoprotein revealed predominance of the RSVA ON1 genotype, in addition to two novel Lebanese genotype variants, hereby named LBA1 and LBA2, which descended from the ON1 and NA2 RSV-A genotypes, respectively. RSVB strains belonged to BA9 genotype except for one BA10. Deduced amino acid sequences depicted several unique substitutions, alteration of glycosylation patterns and the emergence of palivizumab resistance among the Lebanese viruses. The emergence of ON1 and other novel genotypes that are resistant to palivizumab highlights the importance of monitoring RSV globally. © 2019 Abou-El-Hassan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Adolescent, Adult, Antiviral agents, Child, Child, preschool, Drug resistance, viral, Female, Humans, Infant, Lebanon, Male, Middle aged, Models, molecular, Mutation, Palivizumab, Phylogeny, Respiratory syncytial virus infections, Respiratory syncytial virus, human, Respiratory tract infections, Young adult, Attachment glycoprotein, Fusion glycoprotein, Unclassified drug, Virus glycoprotein, Antivirus agent, Aged, Amino acid sequence, Amino acid substitution, Antiviral resistance, Article, Controlled study, Genotype, Human, Human respiratory syncytial virus, Human respiratory syncytial virus a, Human respiratory syncytial virus b, Major clinical study, Monitoring, Nasopharynx, Nonhuman, Nucleotide sequence, Preschool child, School child, Clinical trial, Drug effect, Genetics, Molecular model, Multicenter study, Respiratory syncytial virus infection, Respiratory tract infection, Virology

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