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Volume 27, Number 6—June 2021
Online Report

Proposal for Human Respiratory Syncytial Virus Nomenclature below the Species Level

Vahid Salimi, Mariana Viegas1, Alfonsina Trento1, Charles N. Agoti, Larry J. Anderson, Vasanthi Avadhanula, Justin Bahl, Louis Bont, J. Rodney Brister, Patricia A. Cane, Mónica Galiano, Barney S. Graham, Eneida L. Hatcher, Orienka Hellferscee, David M. Henke, Siddhivinayak Hirve, Sandra Jackson, Els Keyaerts, Leyla Kragten-Tabatabaie, Stephen Lindstrom, Inne Nauwelaers, D. James Nokes, Peter J. Openshaw, Teresa C. Peret, Pedro A. Piedra, Kaat Ramaekers, Annabel Rector, Nídia Sequeira Trovão, Anne von Gottberg, Maria Zambon, Wenqing Zhang, Thomas C. Williams, Ian G. Barr2Comments to Author , and Ursula J. Buchholz2Comments to Author 
Author affiliations: Tehran University of Medical Sciences, Tehran, Iran (V. Salimi); Hospital de Niños Dr. Ricardo Gutiérrez, Buenos Aires, Argentina (M. Viegas); National Center of Biotechnology, Madrid, Spain (A. Trento); KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya (C.N. Agoti, D.J. Nokes); Emory University, Atlanta, Georgia, USA (L.J. Anderson); Baylor College of Medicine, Houston, Texas, USA (V. Avadhanula, D.M. Henke, P.A. Piedra); University of Georgia, Athens, Georgia, USA (J. Bahl); University Medical Center, Utrecht, the Netherlands (L. Bont); National Center for Biotechnology Information, Bethesda, Maryland, USA (J.R. Brister, E.L. Hatcher); Public Health England, London, UK (P.A. Cane, M. Galiano, I. Nauwelaers, M. Zambon); Francis Crick Institute, London (M. Galiano); National Institute of Allergy and Infectious Diseases, Bethesda (B.S. Graham, U.J. Buchholz); National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa (O. Hellferscee, A. von Gottberg); W; orld Health Organization, Geneva, Switzerland (S. Hirve, S. Jackson, W. Zhang); University Hospitals Leuven, Leuven, Belgium (E. Keyaerts); ReSViNET Foundation, Zeist, the Netherlands (L. Kragten-Tabatabaie); Julius Clinical, Zeist (L. Kragten-Tabatabaie); Centers for Disease Control and Prevention, Atlanta (S. Lindstrom, T. Peret); Imperial College London, London (I. Nauwelaers, P. Openshaw); Rega Institute, Leuven (K. Ramaekers, A. Rector); Fogarty International Center, Bethesda (N. Sequeira Trovão); University of Edinburgh, Edinburgh, Scotland, UK (T.C. Williams); Peter Doherty Institute for Infection & Immunity, Melbourne, Victoria, Australia (I. Barr)

Cite This Article

Abstract

Human respiratory syncytial virus (HRSV) is the leading viral cause of serious pediatric respiratory disease, and lifelong reinfections are common. Its 2 major subgroups, A and B, exhibit some antigenic variability, enabling HRSV to circulate annually. Globally, research has increased the number of HRSV genomic sequences available. To ensure accurate molecular epidemiology analyses, we propose a uniform nomenclature for HRSV-positive samples and isolates, and HRSV sequences, namely: HRSV/subgroup identifier/geographic identifier/unique sequence identifier/year of sampling. We also propose a template for submitting associated metadata. Universal nomenclature would help researchers retrieve and analyze sequence data to better understand the evolution of this virus.

Human respiratory syncytial virus (HRSV) is the leading cause of severe respiratory illness in children <5 years of age and is associated with substantial illness from lower respiratory tract infections in industrialized countries and substantial illness and death in low- and middle-income countries (15). HRSV also causes severe disease among elderly and high-risk adults (6).

Figure 1

Annual numbers of HRSV whole-genome sequences released in GenBank since publication of the whole-genome sequence of HRSV A2, M74568, in 1993. HRSV, human respiratory syncytial virus.

Figure 1. Annual numbers of HRSV whole-genome sequences released in GenBank since publication of the whole-genome sequence of HRSV A2, M74568, in 1993. HRSV, human respiratory syncytial virus.

In 2016, HRSV was reclassified by the International Committee on Virus Taxonomy (ICTV) into a new family, Pneumoviridae, genus, Orthopneumovirus, and species, Human orthopneumovirus. (7). The wider availability of viral sequencing technologies has increased submissions of HRSV sequences to databases (Figure 1), a trend we anticipate will continue. Although ICTV provides nomenclature standards for virus taxa, there is currently no standardized format for HRSV nomenclature below the species level. Given the current interest in both HRSV and database submissions, a standard nomenclature is needed to simplify studies of the genomic diversity of HRSV strains and variants below the species level. ICTV’s taxonomic reassignment provides us a timely opportunity to propose a universal naming convention for HRSV strains, sequences, and isolates, including a framework for database submissions that are rich in contextual information and associated metadata.

Several large laboratory HRSV surveillance and epidemiology studies are currently in progress. These studies include the World Health Organization’s Global Respiratory Syncytial Virus (WHO RSV) Surveillance Project (https://www.who.int/influenza/rsv), which conducts large-scale testing for HRSV and extensive sequencing of HRSV-positive clinical specimens from >20 countries worldwide. Focused molecular analyses have helped elucidate HRSV household (8) and local (9) transmission dynamics and may guide development of strategies for the control of HRSV transmission. For example, molecular analysis showed that HRSV in healthcare facilities can be acquired from sources within the facility or introduced from the community (10,11).

In temperate climates, annual HRSV epidemics usually occur in winter months; it remains to be seen how social distancing measures and nonpharmaceutical interventions due to the current coronavirus disease (COVID-19) pandemic will affect global HRSV circulation patterns. One of the 2 major genetic and antigenic HRSV subgroups, A or B, usually predominates in alternating years, but both subgroups can also co-circulate in the same season. Early research has shown that subgroup A HRSV is associated with slightly greater clinical severity than subgroup B (12). Disease severity has been correlated with specific strains, genotypes, or clades, but to date, no consistent association has been established between strains (1315), genotypes, or clades (1619) and virulence. Thus, a possible role of different HRSV strains in disease severity remains to be elucidated. The lack of standard nomenclature and the scarcity of rich metadata in databases currently limit and complicate such studies.

Reliable and concise nomenclature systems below the species level are available for measles virus, influenza virus, rotavirus, filovirus isolates (2023), and many other human viral pathogens. A similar nomenclature system tailored to HRSV and its pathology would support the requirements of researchers and the public health community by minimizing information errors when handling, storing, and shipping HRSV samples and when submitting, searching, and displaying sequencing data and associated metadata. Moreover, consistent nomenclature would improve the ability of researchers to pool and analyze data and associated information from different sources. To fill this need, an international group of researchers, in conjunction with the WHO RSV Global Surveillance Project, proposes a concise nomenclature system for HRSV below the species level.

HRSV Genome Organization

Figure 2

A) Schematic overview of the HRSV gene order and comparison of the amino acid identities of the reference strains of subgroups A (HRSV A2, GenBank accession no. M74568/NC_038235) and B (HRSV B1, GenBank accession no. AF013254/NC_001781). B) ICTV-proposed species designation, virus name, and associated GenBank reference sequences. HRSV, human respiratory syncytial virus; ICTV, International Committee on Virus Taxonomy; RefSeq, reference sequence.

Figure 2. A) Schematic overview of the HRSV gene order and comparison of the amino acid identities of the reference strains of subgroups A (HRSV A2, GenBank accession no. M74568/NC_038235) and B...

HRSV has a single-stranded nonsegmented negative-sense RNA genome ≈15,191–15,277 nt long (Figure 2, panel A) (7). The HRSV genome contains 10 genes, each encoding a separate mRNA with a single open reading frame (ORF) (Figure 2, panel A; Table), except for the M2 mRNA, which contains 2 overlapping ORFs. The 11 HRSV proteins are 2 nonstructural proteins (NS1 and NS2), nucleoprotein (N), phosphoprotein (P), matrix protein (M), small hydrophobic envelope protein (SH), attachment glycoprotein (G), fusion glycoprotein (F), the transcription processivity factor (M2–1), RNA regulatory factor (M2–2), and large RNA polymerase protein (L) (Table) (24,25). The F glycoprotein is the major viral neutralization and protective antigen, followed by the G glycoprotein (26).

HRSV Subgroups and Genotype Designations: Status and Outlook

HRSV subgroups A and B exhibit genomewide nucleotide and amino acid divergence (Figure 2, panel A) (25,27). The reference sequences for the 2 subgroups are derived from strains HRSV A2 (2831; GenBank accession number M74568.1; RefSeq accession number NC_038235) and HRSV B1 (32; GenBank accession number AF013254.1; RefSeq accession number NC_001781.1; Figure 2, panel B). F glycoprotein sequences between the 2 subgroups are well conserved (89% aa identity), whereas the G glycoproteins are the most divergent (53% aa identity between the subgroups) among the HRSV proteins (Figure 2, panel A) and undergo continuous molecular evolution. The ectodomain of the G glycoproteins of both subgroups contains a conserved central domain, representing an important antigenic site, flanked by 2 hypervariable domains (33). Except for the central conserved region, the antigenic cross-reactivity between G glycoproteins of the 2 subgroups is low (26).

Because the G ORF exhibits the greatest degree of genetic variability between isolates, it is most commonly used for studies on the molecular evolution of HRSV. The genetic variability of HRSV strains over time has been commonly determined by sequencing the distal C-terminal third of the G ORF, which includes the second hypervariable domain. The variability in the G ORF is characterized by a high rate of nonsynonymous nucleotide changes, suggesting that evolution may be driven by immune pressure, even though this factor may be partially antibody independent (34). It is likely that variability in the G protein contributes to the capacity of HRSV to cause yearly outbreaks in the community (3537). The nomenclature proposal outlined herein will be useful for the sequence analyses required to follow the molecular evolution of HRSV.

In a parallel effort, several research groups are working together on a genotyping proposal to provide a consensus on uniform genotype designations (38,39). As virus evolution continues, we expect new genotypes to emerge and older genotypes to become extinct. HRSV genotyping designations will need to capture present molecular evolutionary status and be adaptable to changes and will need to be reevaluated periodically by a global consortium.

Nomenclature Proposal for HRSV Strains and Isolates

For molecular epidemiology studies, a concise standard for short identifiers of specific HRSV sequences, suitable for the short definition lines that give context to a sample and its derived sequence, would be useful. Ideally, concise standardized identifiers should convey key information about each individual sequence in an alignment or phylogram, including source, date, and type, if known. Here, we aim to define this type of common naming convention for HRSV samples and isolates. We also propose using standard names and appropriate annotations for HRSV genes, provide examples to guide the annotation of sequence data during the sequence submission process, and suggest how to submit metadata associated with the source materials of HRSV sequences.

Definition Lines for HRSV Sequence Submissions

Figure 3

Schematic representation of the 5 consensus nomenclature elements of HRSV strains and isolates, with examples (top) and an explanation of each element (bottom). HRSV, human respiratory syncytial virus; ID, identification number; ISO, International Organization for Standardization.

Figure 3. Schematic representation of the 5 consensus nomenclature elements of HRSV strains and isolates, with examples (top) and an explanation of each element (bottom). HRSV, human respiratory syncytial virus; ID, identification...

GenBank records available through the National Center for Biotechnology Information (NCBI) are identified by 2 elements: a unique alphanumeric accession number and a definition line. The definition line is the portion of the identifier commonly associated with GenBank records shown in BLAST results and other searches. Definition lines are generated by the submitter during the sequence submission process and include the species and isolate name (e.g., Human orthopneumovirus isolate HRSV/A/USA/001/2011, complete genome [proposed]). (40). We propose a standardized format to capture 5 sample-specific parameters of HRSV-positive clinical samples or isolates to be included in sequence definition lines compatible with database naming requirements (Figure 3), in this specific order: [virus name abbreviation]/[HRSV subgroup]/[geographic identifier]/[unique sequence identifier]/[year of sampling].

Elements of Sequence Definition
I. Organism name; virus name abbreviation: HRSV

ICTV’s species name, Human orthopneumovirus (7), will be reflected as HRSV in the NCBI definition line. During submission to databases, the organism name can be entered as either Human orthopneumovirus or human respiratory syncytial virus. The abbreviation HRSV should be used in the definition line regardless of which organism name is provided.

II. HRSV subgroup: A or B; X, if unknown
III. Geographic identifier for the location of sampling. Because individual HRSV research networks have predefined requirements, we suggest some flexibility for this field:
  • If not specified by a research network, the ISO 3166–1 α-3 letter country code (https://www.iso.org/iso-3166-country-codes.html) should be used to indicate the country of sampling (XXX, if unknown). We strongly suggest that submitters provide any more specific geographic information on the sampling location (e.g., city or state) in metadata fields rather than in the definition line.

  • The WHO Global RSV Surveillance Project plans to use just the simple English-language name for the country.

  • Individual national studies may require a state, province, or city designation, in addition to the mandatory country name. If required, a period should be used to set off the country name ([state/province/city].[country name]).

IV. Unique isolate identifier

This field must be restricted to 8 alphanumeric characters. Underscores are permitted, but neither other special characters (e.g., /, %, $, @) nor spaces can be used. Controversial names or phrases, names of prominent people, and trademarked names or phrases cannot be used. To prevent duplication of sample or isolate identifiers by different groups, we recommend inserting a lettercode identifying a study or institute before the sample number. For example, unique isolate identifiers for samples from the INFORM-RSV study might use “INF” followed by a number (e.g., INF001 in HRSV/A/COUNTRY/INF001/2019).

V. Year of sampling; YYYY or XXXX, if unknown.
Examples of Sequence Definition Lines Using Proposed Nomenclature
  • HRSV/A/USA/001/2011

  • HRSV/B/Denver.USA/14617/1985

  • HRSV/A/IRN/001/2017

  • HRSV/A/Iran/001/2017

  • HRSV/X/IRN/001/2017 (subgroup unknown)

  • HRSV/B/New_Zealand/FR123/2020

Our nomenclature proposal prioritizes a short, concise definition line that will be easy to use in the laboratory, easily readable, and be a uniform system for HRSV in public databases. Additional host, virus, location or temporal information if desired could be submitted in metadata fields, which would allow researchers, epidemiologists, and database users to apply specific metadata filters, as needed for data retrieval and specific applications, analyses, or for displaying designations, such as in dendrograms.

Terminology for Annotations

Figure 4

Schematic aid to gene annotations of HRSV whole-genome sequences. An HRSV gene comprises the sequence from the first nucleotide of the conserved HRSV gene start signal (GGGGCAAATa) to the last adenosine residue of the HRSV gene end signal (AGTTAnnnnAAAA) (25,41). Gene start signals are represented by black triangles, and gene end signals are shown as black rectangles, separated by intergenic regions (underlined). Note the M2/L gene overlap (annotations derived from HRSV A2; GenBank accession no. M74568/NC_038235). le, leader region; HRSV, human respiratory syncytial virus; tr, trailer region.

Figure 4. Schematic aid to gene annotations of HRSV whole-genome sequences. An HRSV gene comprises the sequence from the first nucleotide of the conserved HRSV gene start signal (GGGGCAAATa) to the last...

To support efficient data analysis, uniform designations must be used at the database submission stage. Commonly accepted names for HRSV genes and proteins are shown in the table. An HRSV gene comprises a gene start signal GGGGCAAAT(A/G), an ORF with adjacent noncoding regions, if present, and the gene end signal through the last adenosine residue [AGT(T/A)A(T/A/G)(A/T)(A/T)(A/T)An] (Figure 4; 41). Each HRSV gene contains a single ORF, except for the M2 gene, which has 2 overlapping ORFs, M2–1 and M2–2. Nucleotide annotations of genes and ORFs for the HRSV A2 (Figure 4) and HRSV B1 reference sequences are shown in the table.

Metadata for HRSV Sequence Submissions

What is the most pertinent host data will depend on the interests and objectives of individual study groups. For example, when studying HRSV in a pediatric setting, prematurity may be of interest, but when studying HRSV in an adult setting, researchers may be more interested in whether participants are immunocompromised. We suggest information that could be included in metadata fields for HRSV:

1. Isolation source: sample type (upper or lower airways)
  • Viral RNA can be extracted directly from a clinical sample, from an isolate grown in cell culture, or possibly from a cDNA-derived recombinant virus. The sources of sequences from isolated viruses can be identified by the following designations:

    • wt: wild-type; sequences derived from RNA extracted directly from clinical specimens

    • tc: tissue culture; sequences derived from RNA extracted from HRSV isolates propagated in tissue culture

    • rec: recombinant; sequences of cDNA-derived recombinant virus (including vaccine strain)

2. Host:
Homo sapiens; subject age. Indicate years and months if <5 years of age, years only if ≥5 years of age. Sex should be spelled out if known.
3. Country, state, and (nearest) city of sampling.
Metadata information must include the full country name (not the 3-letter abbreviation) from the NCBI list of accepted country designations (https://www.ncbi.nlm.nih.gov/GenBank/collab/country). City, state, or province can also be included. Names should be written based on the standard ASCII letters including spaces if required (https://www.nist.gov/system/files/documents/2021/03/23/ansi-nist_2010_traditional_encoding.pdf). Geolocation coordinates of the location where sampling took place should be included if known.
4. Collection date
We highly recommend that the exact date of specimen collection (DD-Mon-YYYY format; e.g., 17-Feb-2002) be used; if exact date is not known, at least the month and year should be indicated (Mon-YYYY format).
5. Genotype according to the consensus in genotype classification by an HRSV working group [in progress (38,39)].
Associated with the International RSV Society, a special interest group of the International Society for Influenza and other respiratory viruses https://www.isirv.org/site/index.php/special-interest-groups/international-respiratory-syncytial-virus-society.
6. Metadata on the patient-host and the clinical disease should be included in the notes field in a structured format. Protected personally identifiable health information will be excluded from metadata submissions.
  • If >6 months of age, birthweight and gestational age at birth.

  • Significant pediatric co-morbidities, including prematurity, congenital cardiac disease, and broncho-pulmonary dysplasia (BPD).

  • Twin? (Y/N)

  • Exposed to specific HRSV therapeutic, vaccine, antibody, or antiviral? (Y/N)

  • Viral or bacterial co-infections, if known; pathogen species should be spelled out.

  • Adult underlying conditions, such as chronic obstructive pulmonary disease (COPD) or asthma, or altered immune status (e.g., immunocompromised, bone marrow transplant recipient).

  • Disease outcomes. Five grades are distinguished:

    • No medical care.

    • Outpatient or emergency room.

    • Hospital admission.

    • ICU admission.

    • Death.

For NCBI submissions, data can be entered through the web interface, or uploaded as tab-delimited text files. Sequences can be uploaded in FASTA format (https://blast.ncbi.nlm.nih.gov; Appendix), with associated metadata provided in a plain text, tab-delimited, source modifier table (Appendix Table 1) and gene or protein annotations provided in a plain text, tab-delimited, 5-column feature table (Appendix Table 2).

Outlook

Molecular surveillance has revealed that multiple HRSV genotypes circulate simultaneously in communities. Circulating genotypes often vary between communities, and circulation patterns within a community can change from year to year. Extended monitoring of circulating viruses is necessary to better understand transmission and molecular evolution (42). As HRSV vaccine candidates and antivirals are being developed, molecular epidemiology studies may reveal potential effects of prevention strategies on viral evolution and possible antibody-escape variants. Timely sharing of HRSV data worldwide through the use of public databases is essential. We propose that sequence data be uploaded to publicly accessible databases, such as NCBI (31). Although NCBI is the most complete repository for HRSV sequence information, studies may require that sequences first be submitted to other databases, such as GISAID (https://www.gisaid.org).

Public access will provide useful availability for investigators to submit, query, and analyze HRSV sequence data, enabling the evolutionary analysis of sequence diversity within or between HRSV genotypes. The utility of public access has been clearly demonstrated with the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the critical role that genetic sequence analysis has played. Notably, a nomenclature model for SARS-CoV-2 similar to what we have proposed for HRSV has been adopted, although some differences remain between databases (e.g., NCBI, SARS-CoV-2/human/USA/COVID20–1096/2020; GISAID, hCoV-19/Australia/VIC12/2020). When an HRSV vaccine becomes available, high-quality, geographically representative, country-specific data on circulating strains and rich datasets of well-curated, standardized, and parsable data will be required to monitor and trace possible evolutionary changes in response to vaccine-induced selective pressure (43,44). This proposal will profit from strong support by members of the International RSV Society, a special interest group of the International Society for Influenza and other Respiratory Virus Diseases (https://isirv.org), members of the WHO Global RSV Surveillance Project, and the HRSV research community.

Dr. Salimi is a virologist, associate professor, and head of the virology department at the School of Public Health, Tehran University of Medical Sciences. His primary research interests include genetic characterization, immunopathogenesis, and vaccine design of respiratory viruses.

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Acknowledgments

This manuscript is dedicated to the memory of Jose A. Melero, a superb scientist and leader in the HRSV field and a wonderful and generous friend to us all.

Support for this work was provided by the Intramural Research Programs of the Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health. M.Z. was supported by Public Health England (PHE), and I.N. was supported by PHE and by the National Institute of Health Research (NIHR) Respiratory Health Protection Unit. The work of J.R.B. and E.L.H. was supported by the Intramural Research Program of the National Library of Medicine, National Institutes of Health. T.C.W. was the recipient of a Wellcome Trust Award [204802/Z/16/Z]. The WHO’s Global RSV Surveillance is supported by the Bill and Melinda Gates Foundation grant award no. OPP1127419.

S.H., S.J., and W.Z. work with the World Health Organization. The authors are responsible for the views expressed in this publication and they do not necessarily represent the decisions, policy or views of the World Health Organization. Names of specific vendors, manufacturers, or products are included for public health and informational purposes; inclusion does not imply endorsement of the vendors, manufacturers, or products by the World Health Organization. L.A. has done paid consultancies on RSV vaccines for Bavarian Nordic, Novavax, ClearPath Vaccines Company, and Pfizer; his laboratory is currently receiving funding through Emory University from Pfizer and Advac for laboratory studies for HRSV surveillance studies in adults, and he holds a subcontract on an NIH SBIR award to Sciogen on G protein HRSV vaccines. L.A. is a co-inventor on several CDC patents on the HRSV G protein and its CX3C chemokine motif relative to immune therapy and vaccine development, and on a patent filing for use of HRSV platform VLPs with the F and G proteins for vaccines. U.B. reports CRADA support to NIH from Sanofi Pasteur, outside the submitted work; in addition, she has patents on live-attenuated HRSV with royalties paid to NIH by Sanofi Pasteur. There are no additional conflicts of interest by any of the authors.

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References

  1. Shi  T, McAllister  DA, O’Brien  KL, Simoes  EAF, Madhi  SA, Gessner  BD, et al.; RSV Global Epidemiology Network. Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in young children in 2015: a systematic review and modelling study. Lancet. 2017;390:94658. DOIPubMed
  2. Nair  H, Nokes  DJ, Gessner  BD, Dherani  M, Madhi  SA, Singleton  RJ, et al. Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet. 2010;375:154555. DOIPubMed
  3. Salimi  V, Tavakoli-Yaraki  M, Yavarian  J, Bont  L, Mokhtari-Azad  T. Prevalence of human respiratory syncytial virus circulating in Iran. J Infect Public Health. 2016;9:12535. DOIPubMed
  4. Stein  RT, Bont  LJ, Zar  H, Polack  FP, Park  C, Claxton  A, et al. Respiratory syncytial virus hospitalization and mortality: Systematic review and meta-analysis. Pediatr Pulmonol. 2017;52:55669. DOIPubMed
  5. O’Brien  KL, Baggett  HC, Brooks  WA, Feikin  DR, Hammitt  LL, Higdon  MM, et al.; Pneumonia Etiology Research for Child Health (PERCH) Study Group. Causes of severe pneumonia requiring hospital admission in children without HIV infection from Africa and Asia: the PERCH multi-country case-control study. Lancet. 2019;394:75779. DOIPubMed
  6. Falsey  AR, Hennessey  PA, Formica  MA, Cox  C, Walsh  EE. Respiratory syncytial virus infection in elderly and high-risk adults. N Engl J Med. 2005;352:174959. DOIPubMed
  7. Rima  B, Collins  P, Easton  A, Fouchier  R, Kurath  G, Lamb  RA, et al.; Ictv Report Consortium. ICTV virus taxonomy profile: Pneumoviridae. J Gen Virol. 2017;98:29123. DOIPubMed
  8. Agoti  CN, Phan  MVT, Munywoki  PK, Githinji  G, Medley  GF, Cane  PA, et al. Genomic analysis of respiratory syncytial virus infections in households and utility in inferring who infects the infant. Sci Rep. 2019;9:10076. DOIPubMed
  9. Trovao  NS, Khuri-Bulos  N, Tan  Y, Puri  V, Shilts  MH, Halpin  RA, et al. Molecular characterization of respiratory syncytial viruses circulating in a paediatric cohort in Amman, Jordan. Microb Genom. 2019 Sep 18 [Epub ahead of print].
  10. Geis  S, Prifert  C, Weissbrich  B, Lehners  N, Egerer  G, Eisenbach  C, et al. Molecular characterization of a respiratory syncytial virus outbreak in a hematology unit in Heidelberg, Germany. J Clin Microbiol. 2013;51:15562. DOIPubMed
  11. Nabeya  D, Kinjo  T, Parrott  GL, Uehara  A, Motooka  D, Nakamura  S, et al. The clinical and phylogenetic investigation for a nosocomial outbreak of respiratory syncytial virus infection in an adult hemato-oncology unit. J Med Virol. 2017;89:136472. DOIPubMed
  12. Hall  CB, Walsh  EE, Schnabel  KC, Long  CE, McConnochie  KM, Hildreth  SW, et al. Occurrence of groups A and B of respiratory syncytial virus over 15 years: associated epidemiologic and clinical characteristics in hospitalized and ambulatory children. J Infect Dis. 1990;162:128390. DOIPubMed
  13. Malekshahi  SS, Razaghipour  S, Samieipoor  Y, Hashemi  FB, Manesh  AAR, Izadi  A, et al. Molecular characterization of the glycoprotein and fusion protein in human respiratory syncytial virus subgroup A: Emergence of ON-1 genotype in Iran. Infect Genet Evol. 2019;71:16678. DOIPubMed
  14. Vos  LM, Oosterheert  JJ, Kuil  SD, Viveen  M, Bont  LJ, Hoepelman  AIM, et al. High epidemic burden of RSV disease coinciding with genetic alterations causing amino acid substitutions in the RSV G-protein during the 2016/2017 season in The Netherlands. J Clin Virol. 2019;112:206. DOIPubMed
  15. Pierangeli  A, Viscido  A, Bitossi  C, Frasca  F, Gentile  M, Oliveto  G, et al. Differential interferon gene expression in bronchiolitis caused by respiratory syncytial virus-A genotype ON1. Med Microbiol Immunol (Berl). 2020;209:238. DOIPubMed
  16. Vandini  S, Biagi  C, Lanari  M. Respiratory syncytial virus: the influence of serotype and genotype variability on clinical course of infection. Int J Mol Sci. 2017;18:1717. DOIPubMed
  17. Laham  FR, Mansbach  JM, Piedra  PA, Hasegawa  K, Sullivan  AF, Espinola  JA, et al. Clinical profiles of respiratory syncytial virus subtypes A and B among children hospitalized with bronchiolitis. Pediatr Infect Dis J. 2017;36:80810. DOIPubMed
  18. Gilca  R, De Serres  G, Tremblay  M, Vachon  ML, Leblanc  E, Bergeron  MG, et al. Distribution and clinical impact of human respiratory syncytial virus genotypes in hospitalized children over 2 winter seasons. J Infect Dis. 2006;193:548. DOIPubMed
  19. Martinello  RA, Chen  MD, Weibel  C, Kahn  JS. Correlation between respiratory syncytial virus genotype and severity of illness. J Infect Dis. 2002;186:83942. DOIPubMed
  20. Measles virus nomenclature update: 2012. Wkly Epidemiol Rec. 2012;87:7381.PubMed
  21. Kuhn  JH, Bao  Y, Bavari  S, Becker  S, Bradfute  S, Brister  JR, et al. Virus nomenclature below the species level: a standardized nomenclature for laboratory animal-adapted strains and variants of viruses assigned to the family Filoviridae. Arch Virol. 2013;158:142532. DOIPubMed
  22. Matthijnssens  J, Ciarlet  M, McDonald  SM, Attoui  H, Bányai  K, Brister  JR, et al. Uniformity of rotavirus strain nomenclature proposed by the Rotavirus Classification Working Group (RCWG). Arch Virol. 2011;156:1397413. DOIPubMed
  23. Reconsideration of influenza A virus nomenclature: a WHO memorandum. Bull World Health Organ. 1979;57:22733.PubMed
  24. Collins  PL, Fearns  R, Graham  BS. Respiratory syncytial virus: virology, reverse genetics, and pathogenesis of disease. Curr Top Microbiol Immunol. 2013;372:338. DOIPubMed
  25. Collins  PL, Karron  RA. Respiratory syncytial virus and metapneumovirus. In: Knipe DM, Howley PM, Cohen JI, Griffin DE, Lamb RA, Martin MA, et al., editors. Fields Virology. 6th ed. Philadelphia: Lippincott Williams & Wilkins; 2013. p. 1086–123.
  26. Collins  PL, Melero  JA. Progress in understanding and controlling respiratory syncytial virus: still crazy after all these years. Virus Res. 2011;162:8099. DOIPubMed
  27. Mufson  MA, Orvell  C, Rafnar  B, Norrby  E. Two distinct subtypes of human respiratory syncytial virus. J Gen Virol. 1985;66:211124. DOIPubMed
  28. Collins  PL, Olmsted  RA, Spriggs  MK, Johnson  PR, Buckler-White  AJ. Gene overlap and site-specific attenuation of transcription of the viral polymerase L gene of human respiratory syncytial virus. Proc Natl Acad Sci U S A. 1987;84:51348. DOIPubMed
  29. Mink  MA, Stec  DS, Collins  PL. Nucleotide sequences of the 3′ leader and 5′ trailer regions of human respiratory syncytial virus genomic RNA. Virology. 1991;185:61524. DOIPubMed
  30. O’Leary  NA, Wright  MW, Brister  JR, Ciufo  S, Haddad  D, McVeigh  R, et al. Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation. Nucleic Acids Res. 2016;44(D1):D73345. DOIPubMed
  31. Sayers  EW, Beck  J, Brister  JR, Bolton  EE, Canese  K, Comeau  DC, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. 2020;48(D1):D916. DOIPubMed
  32. Karron  RA, Buonagurio  DA, Georgiu  AF, Whitehead  SS, Adamus  JE, Clements-Mann  ML, et al. Respiratory syncytial virus (RSV) SH and G proteins are not essential for viral replication in vitro: clinical evaluation and molecular characterization of a cold-passaged, attenuated RSV subgroup B mutant. Proc Natl Acad Sci U S A. 1997;94:139616. DOIPubMed
  33. Martínez  I, Dopazo  J, Melero  JA. Antigenic structure of the human respiratory syncytial virus G glycoprotein and relevance of hypermutation events for the generation of antigenic variants. J Gen Virol. 1997;78:241929. DOIPubMed
  34. Trento  A, Ábrego  L, Rodriguez-Fernandez  R, González-Sánchez  MI, González-Martínez  F, Delfraro  A, et al. Conservation of G-protein epitopes in respiratory syncytial virus (group A) despite broad genetic diversity: is antibody selection involved in virus evolution? J Virol. 2015;89:777685. DOIPubMed
  35. Melero  JA, García-Barreno  B, Martínez  I, Pringle  CR, Cane  PA. Antigenic structure, evolution and immunobiology of human respiratory syncytial virus attachment (G) protein. J Gen Virol. 1997;78:24118. DOIPubMed
  36. Sullender  WM, Mufson  MA, Anderson  LJ, Wertz  GW. Genetic diversity of the attachment protein of subgroup B respiratory syncytial viruses. J Virol. 1991;65:542534. DOIPubMed
  37. Cane  PA, Matthews  DA, Pringle  CR. Analysis of respiratory syncytial virus strain variation in successive epidemics in one city. J Clin Microbiol. 1994;32:14. DOIPubMed
  38. Goya  S, Galiano  M, Nauwelaers  I, Trento  A, Openshaw  PJ, Mistchenko  AS, et al. Toward unified molecular surveillance of RSV: A proposal for genotype definition. Influenza Other Respir Viruses. 2020;14:27485. DOIPubMed
  39. Ramaekers  K, Rector  A, Cuypers  L, Lemey  P, Keyaerts  E, Van Ranst  M. Towards a unified classification for human respiratory syncytial virus genotypes. Virus Evol. 2020;6:veaa052.
  40. The GenBank Submissions Handbook. Bethesda (MD): National Center for Biotechnology Information; 2011.
  41. Collins  PL, Dickens  LE, Buckler-White  A, Olmsted  RA, Spriggs  MK, Camargo  E, et al. Nucleotide sequences for the gene junctions of human respiratory syncytial virus reveal distinctive features of intergenic structure and gene order. Proc Natl Acad Sci U S A. 1986;83:45948. DOIPubMed
  42. Trento  A, Casas  I, Calderón  A, Garcia-Garcia  ML, Calvo  C, Perez-Breña  P, et al. Ten years of global evolution of the human respiratory syncytial virus BA genotype with a 60-nucleotide duplication in the G protein gene. J Virol. 2010;84:750012. DOIPubMed
  43. Graham  BS. Vaccine development for respiratory syncytial virus. Curr Opin Virol. 2017;23:10712. DOIPubMed
  44. Mazur  NI, Higgins  D, Nunes  MC, Melero  JA, Langedijk  AC, Horsley  N, et al.; Respiratory Syncytial Virus Network (ReSViNET) Foundation. The respiratory syncytial virus vaccine landscape: lessons from the graveyard and promising candidates. Lancet Infect Dis. 2018;18:e295311. DOIPubMed
  45. Collins  PL, Hill  MG, Camargo  E, Grosfeld  H, Chanock  RM, Murphy  BR. Production of infectious human respiratory syncytial virus from cloned cDNA confirms an essential role for the transcription elongation factor from the 5′ proximal open reading frame of the M2 mRNA in gene expression and provides a capability for vaccine development. Proc Natl Acad Sci U S A. 1995;92:115637. DOIPubMed
  46. Crowe  JE Jr, Bui  PT, Firestone  CY, Connors  M, Elkins  WR, Chanock  RM, et al. Live subgroup B respiratory syncytial virus vaccines that are attenuated, genetically stable, and immunogenic in rodents and nonhuman primates. J Infect Dis. 1996;173:82939. DOIPubMed

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DOI: 10.3201/eid2706.204608

Original Publication Date: May 10, 2021

1These authors contributed equally to this article.

2These last authors contributed equally to this article.

Table of Contents – Volume 27, Number 6—June 2021

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Ian Barr, Peter Doherty Institute for Infection & Immunity, 792 Elizabeth Street , Melbourne, VIC 3000, Australia

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