Abstract

Rhinoviruses (RVs) are increasingly implicated not only in mild upper respiratory tract infections, but also in more severe lower respiratory tract infections; however, little is known about species diversity and viral epidemiology of RVs among the infected children. Therefore, we investigated the rhinovirus (RV) infection prevalence over a 2-year period, compared it with prevalence patterns of other common respiratory viruses, and explored clinical and molecular epidemiology of RV infections among 590 children hospitalized with acute respiratory infection in north-western and central parts of Croatia. For respiratory virus detection, nasopharyngeal and pharyngeal flocked swabs were taken from each patient and subsequently analyzed with multiplex RT-PCR. To determine the RV species in a subset of positive children, 5′UTR in RV-positive samples has been sequenced. Nucleotide sequences of referent RV strains were retrieved by searching the database with Basic Local Alignment Tool, and used to construct alignments and phylogenetic trees using MAFFT multiple sequence alignment tool and the maximum likelihood method, respectively. In our study population RV was the most frequently detected virus, diagnosed in 197 patients (33.4%), of which 60.4% was detected as a monoinfection. Median age of RV-infected children was 2.25 years, and more than half of children infected with RV (55.8%) presented with lower respiratory tract infections. Most RV cases were detected from September to December, and all three species co-circulated during the analyzed period (2017–2019). Sequence analysis based on 5′UTR region yielded 69 distinct strains; the most prevalent was RV-C (47.4%) followed by RV-A (44.7%) and RV-B (7.9%). Most of RV-A sequences formed a distinct phylogenetic group; only strains RI/HR409-18 (along with a reference strain MF978777) clustered with RV-C strains. Strains belonging to the group C were the most diverse (41.6% identity among strains), while group B was the most conserved (71.5% identity among strains). Despite such differences in strain groups (hitherto undescribed in Croatia), clinical presentation of infected children was rather similar. Our results are consistent with newer studies that investigated the etiology of acute respiratory infections, especially those focused on children with lower respiratory tract infections, where RVs should always be considered as potentially serious pathogens.

Highlights

  • Rhinoviruses (RVs) are small, non-enveloped viruses that belong to the family Picornaviridae, genus Enterovirus

  • There are differences between RV species in utilization of cell entry receptor: a majority of RV-A and RV-B attach to the intercellular adhesion molecule (ICAM)-1 and the others alternatively bind low density lipoprotein receptor (LDL-R), whereas RV-C utilizes human cadherin-related family member 3 (CDHR3) (Bochkov et al, 2015; Royston and Tapparel, 2016)

  • In this study we initially evaluated the prevalence of RV and other common respiratory viruses, as well as RV species distribution in hospitalized children with symptoms of acute respiratory tract infection (ARI) over a period of 2 years

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Summary

Introduction

Rhinoviruses (RVs) are small, non-enveloped viruses that belong to the family Picornaviridae, genus Enterovirus. There are 171 rhinovirus (RV) genotypes recognized and classified into the three species as RV-A (83 types), RV-B (32 types), and RV-C (56 types) (Royston and Tapparel, 2016; Pan et al, 2018). There are differences between RV species in utilization of cell entry receptor: a majority of RV-A and RV-B attach to the intercellular adhesion molecule (ICAM)-1 (classified as the major receptor group) and the others alternatively bind low density lipoprotein receptor (LDL-R) (minor receptor group), whereas RV-C utilizes human cadherin-related family member 3 (CDHR3) (Bochkov et al, 2015; Royston and Tapparel, 2016). Rhinovirus genome is a 7.2-kb single-stranded, positive-sense RNA with a single open reading frame (ORF) joined to a 5 untranslated region (5 UTR) and a short viral priming protein (VPg) (Jacobs et al, 2013). A rather conserved 5 UTR region that harbors internal ribosomal entry site (IRES) is usually utilized for RV detection from clinical samples, while more precise genotyping is based on VP4/VP2 or VP1 sequence analysis

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