Volume 20, Number 6—June 2014
Rapid Spread and Diversification of Respiratory Syncytial Virus Genotype ON1, Kenya
Respiratory syncytial virus genotype ON1, which is characterized by a 72-nt duplication in the attachment protein gene, has been detected in >10 countries since first identified in Ontario, Canada, in 2010. We describe 2 waves of genotype ON1 infections among children admitted to a rural hospital in Kenya during 2012. Phylogenetic analysis of attachment protein gene sequences showed multiple introductions of genotype ON1; variants distinct from the original Canadian viruses predominated in both infection waves. The genotype ON1 dominated over the other group A genotypes during the second wave, and some first wave ON1 variants reappeared in the second wave. An analysis of global genotype ON1 sequences determined that this genotype has become considerably diversified and has acquired signature coding mutations within immunogenic regions, and its most recent common ancestor dates to ≈2008–2009. Surveillance of genotype ON1 contributes to an understanding of the mechanisms of rapid emergence of respiratory viruses.
Human respiratory syncytial virus (RSV) is the major viral cause of bronchiolitis and pneumonia in infants and also a major cause of severe respiratory illness in the elderly (1). RSV infection usually occurs in annual epidemics, and the virus can re-infect persons throughout life. RSV isolates fall into 2 groups, A and B, and each group includes multiple genotypes. RSV epidemics are often caused by several variants of >1 RSV genotypes, and the dominant genotype is usually replaced each year (2). RSV’s most variable protein, the attachment (G) glycoprotein, is also a target of protective antibody responses, and analysis of its encoding genome portion shows continuous accumulation of genetic changes leading to antigenic drift (3,4). However, as a nonsegmented, single-stranded RNA virus, RSV does not show the abrupt antigenic changes that are sometimes seen in influenza A viruses. The abrupt changes in influenza A viruses commonly arise when genome segments reassort, sometimes acquiring new surface protein genes from animal sources, leading to antigenic shift as was seen in the recent influenza A(H1N1) pandemic strain (5). Nevertheless, twice in recent years, a distinct new genotype of RSV has arisen as a result of duplication within the G gene. The first of these new genotypes was detected in 1999 when 3 group B viruses with a 60-nt duplication in the C-terminal region of the G gene, which encodes strain-specific epitopes (4), were isolated in Buenos Aires, Argentina (6). This genotype was also observed in a retrospective analysis of RSV samples from 1998 to 1999 in Madrid, Spain (7). This novel genotype spread rapidly and by 2003 was being detected around the world; by 2006, it had become the predominant group B genotype (7,8).
In December 2010, a novel RSV group A genotype, ON1, with a 72-nt duplication in the C-terminal region of the G gene, was detected in Ontario, Canada (9). This genotype was also detected in Malaysia, India, and South Korea at the end of 2011 (10–12) and in Germany, Italy, South Africa, Japan, China, and Kenya in 2012 (13–15) (GenBank, unpub. data). The emergence and spread of these new genotypes, which can be readily tracked by G gene sequencing, provide an opportunity to re-examine 1) the interconnectedness of RSV epidemics at various levels (e.g., global, country, and community levels), 2) the spatial–temporal scale of the spread of variants, and 3) the pace and nature of associated genetic changes. Such examinations have the potential to bring new insights regarding how RSV persists to cause recurrent epidemics in human populations.
We conducted a detailed analysis of G gene variability of the ON1 genotype viruses detected among children inpatients at a hospital in rural Kenya in 2012. Two RSV epidemics were observed during the year, and a wave of genotype ON1 cases occurred in each. We compare the phylogenetic relationship between the ON1 viruses detected in Kenya and ON1 viruses worldwide during a similar period.
Study Location and Participants
The study specimens were obtained from children <5 years of age who had been admitted with severe pneumonia to Kilifi District Hospital (KDH), Kenya, during 2012. All children were enrolled as part of an ongoing study, initiated in 2002, of the epidemiology and disease of RSV-associated pneumonia in case-patients (16–18). KDH, located in the coastal town of Kilifi, north of Mombasa, serves a rural (predominantly) and semiurban community. In this setting, epidemics of RSV disease occur on an annual basis, beginning in late October or early November of each year and continuing through June, July, or August of the next year (18).
Clinical Samples and Laboratory Methods
Since 2002, nasal wash or nasopharyngeal swab specimens have been collected from all children enrolled in the pneumonia study. The samples are tested for the presence of RSV antigen and/or nucleic acid by using the indirect fluorescence antibody test and real-time reverse transcription PCR, respectively (19). G gene sequencing is routinely undertaken on all samples from the KDH study site that have RSV-positive test results (16,20) (J.R. Otieno and colleagues, unpub. data). The ON1 genotype was first detected by this surveillance in February 2012. This report focuses on RSV A specimens collected during 2012.
Viral RNA extraction, reverse transcription, PCR amplification, and sequencing of the G gene were undertaken as described (16,20,21). The specimens were collected after informed consent was given by a parent or guardian for each child. The Kenya National Ethics Review body approved the study protocols.
Sequence Alignments and Comparison Dataset
Consensus G gene sequences for RSV A were initially aligned in MAFFT v6.884b (22) and trimmed in BioEdit (http://www.mbio.ncsu.edu/bioedit/bioedit.html). Viruses possessing the ON1 72-nt duplication were readily identifiable from the alignments. Sequences for Kilifi viruses corresponded to the terminal 702 nt and 630 nt in the G ectodomain regions of ON1 and non-ON1 viruses, respectively. A comparison dataset of ON1 genotype sequences deposited into GenBank was downloaded, collated, aligned with the Kilifi ON1 sequences, and used to derive a global phylogenetic tree. Because some sequences were limited in length, the final worldwide ON1 alignment was trimmed to include only the C-terminal G gene region over the terminal 333 nt.
Phylogenetic trees were constructed in MEGA5.2.1 (23) by using the maximum likelihood method under the general time-reversible model of evolution. The robustness of the phylogenetic clusters was evaluated by bootstrapping with 1,000 iterations. Viruses were considered to be the same variant if they were identical in nucleotide sequence over the region we sequenced. Variants were grouped into a similar lineage if they shared signature-coding mutations. The Kilifi sequences reported here are deposited in GenBank under accession numbers KF587911–KF588014.
The rate of evolution of the ON1 G gene and the date of the most recent common ancestor (MRCA) of the viruses collected to date were estimated by 2 independent methods: 1) by using regression of the root-to-tip distances from the maximum-likelihood tree in Path-O-gen (http://tree.bio.ed.ac.uk/software/pathogen/) and 2) by using the BEAST v1.74 analysis package (https://code.google.com/p/beast-mcmc/), which uses the Bayesian Markov chain Monte Carlo approach (24). The analysis included only sequences for which the exact date of sampling was provided. Furthermore, to reduce the bias of oversampling from any 1 location, we included only viruses with unique nucleotide sequences in the C-terminus region in the analysis. The final data subset comprised 65 sequences from 7 countries.
The BEAST analysis was run through 50 million steps, with sampling every 2,500 steps, under the HKY model of evolution and the Bayesian skyride population growth model. Once the analysis was complete, run convergence was confirmed by using the Tracer v1.5 program (http://tree.bio.ed.ac.uk/software/tracer/); trees were summarized in TreeAnnotator and visualized in FigTree v1.40 (http://tree.bio.ed.ac.uk/software/figtree/).
During January 1–December 31, 2012, a total of 873 children who were admitted to KDH were eligible for the RSV surveillance study. Nasal wash or nasopharyngeal swab specimens were obtained from 834 of the children and tested for RSV. Of the 834 samples, 240 (28.8%) were RSV positive: 123 (51.3%) were group A infections, 114 (47.5%) were group B infections, and 3 (1.3%) were A/B co-infections. Of the 126 combined group A and group A/B viruses, 104 (82.5%) were successfully sequenced in the G gene ectodomain region, and of these, 77 (74.0%) possessed the ON1 genotype 72-nt duplication. The numbers of RSV A, B, and ON1 cases detected each month at KDH during 2012 are shown in Table 1. The number of cases detected each week is shown in Figure 1, panel A.
Two Waves of RSV Genotype ON1 Infections
The ON1 genotype was first detected in Kilifi in February 2012, which was about the middle of the 2011–12 RSV epidemic. The ON1 viruses continued to be detected along with the other group A viruses through June 2012; in July and August, ON1 was the only RSV A genotype detected, marking the end of the first wave (Table 1). Overall, however, the full 2011–12 RSV epidemic was dominated by group B viruses (65.0%), which co-circulated with the group A genotypes during the epidemic (Table 1, including footnotes; Figure 1, panel A). During the first 8 months of 2012, a total of 31 ON1 infections were detected, representing 20.9% (31/148) of the overall RSV diagnoses and 60.8% (31/51) of the group A diagnoses with known ON1 status (Table 1).
The second wave of ON1 infections in Kilifi started in October 2012 at the beginning of the 2012–13 RSV epidemic, and detection continued up to the last month covered by the surveillance reported here (December 2012) (Table 1). During those 3 months, more cases of group A (75.6%, 68/90) than group B RSV were detected, and the ON1 genotype constituted the majority of the RSV A viruses (86.8%, 46/53) among those successfully sequenced (Table 1). Overall, more ON1 cases were recorded each week during the second infection wave than during the first wave (Figure 1, panel A), and the genotype appeared to predominate the other RSV A genotypes during the second wave (Table 1).
Genetic Variability of ON1 Viruses from the Two Infection Waves
Of the 77 sequenced ON1 viruses, 25 unique nucleotide sequences were identified across the 702 nt–long G gene region: 8 were found only in the first infection wave, 14 were found only in the second wave, and 3 were found in both waves. Phylogenetic analysis of the G gene region of these ON1 genotype Kilifi viruses identified 3 main lineages circulating in Kilifi. The 3 lineages comprised multiple phylogenetic clusters and several singleton sequences (Figure 1, panel B; Figure 2, panel A). Lineage 1 was the first to be identified and included most (84.4%, 65/77) of the Kilifi ON1 viruses. The sequences of this lineage did not fall into a single cluster, but they were closely related and shared signature mutations (Table 2; Technical Appendix [PDF - 631 KB - 2 pages] Figure 1. Lineages 2 (5 viruses) and 3 (7 viruses) were assigned from the 2 phylogenetic clusters that were prominent from the rest of the Kilifi ON1 sequences and on well-supported branches (bootstrap >90%). These lineages most likely represented 2 independent introductions of the ON1 genotype into the Kilifi community during the first infection wave. It is also possible that lineage 1 was introduced multiple times, which would explain its sequence diversity (shown by the multiple small clusters and the singleton sequences). Figure 2, panel B, shows how the 3 Kilifi lineages fit into the global picture on phylogenetic analysis of the C-terminal third region of all ON1 sequences detected throughout the world to date (see detail below).
Persistence of ON1 Variants between Infection Waves
G nucleotide sequences for 24 of 46 ON1 viruses sequenced from the second infection wave were identical to sequences of 3 variants from the first wave (Figures 1, panel B; Figure 2, panel A), suggesting possible sustained transmission of these variants in the community through the interepidemic trough. Two of these first-wave variants were from lineage 1, and the third was from lineage 3. Phylogenetic analysis of viruses from the first and second infection waves (Figure 2, panel A) showed that lineage 1 and 3 viruses were detected during both waves, but lineage 2 was detected only during the first wave (Figure 1, panel B). These persisting first-wave variants were initially detected on February 13, March 23, and August 24, 2012, and they were still being detected in December 2012 (during the second infection wave), the last month of the surveillance reported here.
Genetic Variability of ON1 Viruses Identified Globally
To evaluate the global genetic variability of the ON1 genotype, we combined the G gene sequences from the 77 ON1 viruses from Kenya with 118 ON1 G gene sequences in GenBank from 9 other countries; the GenBank sequences represented all ON1 sequences available as of September 8, 2013. The phylogenetic relationships of these combined ON1 sequences in the G gene are shown in Figure 2, panel B, and in Technical Appendix [PDF - 631 KB - 2 pages] Figure 2 (taxon names provided). Sequences for 72 of the 77 ON1 viruses from Kenya (i.e., all lineage 1 and 3 sequences from the Kilifi data) fell into 1 branch of the global phylogeny. The bootstrap support value for the 72 sequences was low, indicating the presence of just a few unique substitutions. This branch also included 20 viruses from Japan, 2 viruses from Italy, and the 1 virus from India (Technical Appendix [PDF - 631 KB - 2 pages] Figure 2). Of the 20 Japanese viruses within this branch, 12 were identical to 1 of the Kilifi variants that appeared in the first infection wave and persisted into the second wave. The ON1 Kilifi lineage that fell outside this main Kenyan branch (i.e., lineage 2) clustered with the original ON1 viruses from Canada together with ON1 viruses from Germany, Malaysia, and Italy (Figure 2, panel B).
The reconstruction of a phylogenetic tree combining all the global ON1 sequences, from which the duplicated region had been excised, and the non-ON1 sequences detected in Kilifi in 2012 showed that the global ON1 sequences, including those from Kilifi, form a monophyletic cluster away from sequences of non-ON1 viruses. This finding reaffirmed that the Kilifi viruses with the duplication (ON1) did not arise de novo locally (data not shown).
The global geographic locations for which ON1 sequences were available in GenBank as of September 8, 2013, and the number of sequences present by country are shown in Figure 3, panels A and B. The temporal patterns for the detections of the ON1 viruses in Kilifi and in the GenBank dataset are consistent with 2 ON1 infection waves in 2012; the genotype was rare in 2011, despite first being detected in 2010 (Figure 3, panel C).
Signature Amino Acid Substitutions
Several nonsynonymous substitutions were predicted in the first and second hypervariable regions of the ON1 G protein. Signature coding mutations that were observed in >3 viruses are summarized in Table 2, and the amino acid alignment of the deduced G protein C-terminus region from the unique nucleotide sequences among the combined Kenyan ON1 and GenBank collated dataset is shown in Figure 4. Several of the changes within the second hypervariable G region had occurred on codon positions (relative to the prototype strain RSV A2) previously predicted to be positively selected: codons 225, 226, 246, 248, 249, 253, 256, 262, 265, 272, 274–276, 280, and 284–286 (25,28). Four amino acid changes (L274P, L298P, Y304H, and L310P) relative to the original Canadian viruses were shared by most of the viruses from multiple countries and defined the 2 major branches on the phylogenetic tree (Table 2; Figures 2, panel B, and 4). The first 2 of these changes, L274P and L298P, occurred concurrently in most strains and refer to the same positions within the parent and the resulting duplication region; thus, this event is considered noteworthy because the region nearby (aa 265–273) is a reported antigenic site (29). Furthermore, changes were observed in the region that would change the potential N-glycosylation profile from the original Canadian viruses. Some of the changes would cause the loss of a site (e.g., N318H in Ken/113732/28-Jun-2012 and N318F in ITA/Roma/KC858255/2013) and others would cause site gains (e.g., H266N in ITA/Roma/KC858255/2013 and ITA/Roma/KC858257/2012).
Timing of the ON1 Genotype MRCA and Evolution Rate
The MRCA analysis of the combined global ON1 sequences from the root-to-tip genetic distances on the maximum-likelihood tree showed that the ON1 genotype probably arose during the 2008–09 RSV season; the point estimate was August 2008 (Figure 5). The nucleotide substitution rate was estimated to be 7.87 × 10−3 substitutions per site per year in the C-terminus region. The alternative Bayesian methods showed that the global ON1 genotype viruses MRCA probably occurred in December 2009 (95% highest probability density [HPD] interval, 2004.26–2012.10), and the nucleotide substitution rate over the period was estimated to be 5.27 × 10−3 (95% HPD interval; 1.53 × 10−3 to 9.11 × 10−3). Although the Bayesian methods presented a wide estimate interval, both analysis methods indicate that the variant probably arose 1–2 epidemic seasons before its first detection in Ontario.
Our findings reinforce the observation that respiratory viruses, including RSV, can spread rapidly around the world. It has long been known that novel antigenic variants of influenza A spread rapidly over short periods and drive successive epidemics; however, the mechanism of recurrent epidemics or global endemicity for RSV is poorly understood (30). Observation of the emergence and rapid spread and diversification of RSV group B genotype BA (containing a 60-nt duplication) has improved our understanding of the scale of RSV spread and transmission in the world (29). Our findings regarding the ON1 genotype, which also possesses a large nucleotide duplication, closely relate to findings regarding the BA genotype and confirm that novel RSV strains do spread rapidly and widely.
Of particular interest is the observation that within a few years of the generation of these new genotypes, variants have evolved with accumulated signature coding changes in regions of the G protein targeted by the neutralizing antibody response. For example, a previously identified putative epitope around codon 274 was duplicated in the ON1 genotype, and some of the emerging variants have shown amino acid changes in both copies of this epitope (Figure 4). This suggests that such ON1 variants were selected by the change on this particular epitope. Furthermore, in many ON1 variants, additional coding changes are observed at codons previously predicted to be positively selected (25,26,28), at potential N-glycosylation codons (4), and at positions previously reported in escape mutants from certain monoclonal antibodies (e.g., L310P, which in viruses without the duplication will be equivalent to L286P) (27). The P286L change has been associated with abrogation of reaction of peptides to convalescent-phase human serum (31). Thus it may be deduced that the amino acid changes already observed in the ON1 variants have led to profound differences in its antigenic profile.
The presence of the multiple ON1 genotype lineages in Kilifi, some occurring as multiple phylogenetic clusters or several distinct sequences, suggests that there have been multiple introductions of the genotype into the region. Some of these ON1 viruses have partial G gene sequences identical to the few ON1 genotype GenBank sequences available from around the world, indicating that ON1 variants that arose soon after its emergence are also quickly spreading worldwide. We also detected identical ON1 G gene sequences for viruses from the 2 RSV infection waves in Kilifi, which could reflect continued local transmission of the first-wave viruses or further new introductions of identical viruses of the genotype into the community during the second wave.
MRCA analysis determined that ON1 first emerged in 2008 or 2009. This would suggest that the variant was circulating undetected before December 2010, and its first location of occurrence may remain unknown. This estimate of the time between first occurrence and detection is shorter than the ≈12 years proposed by Tsukagoshi et al. (13). Overall, by both the maximum likelihood and Bayesian methods, we estimated that this variant had a higher rate of evolution in its C-terminus region (point estimates of >5.0 × 10−3 nucleotide substitutions per site per year) than previously predicted for RSV A (3.382 × 10−3 [95% HPD interval 1.911 × 10−3 to 4.954 × 10−3]) (32). This finding suggested an accelerated evolution rate in this variant early in its lifetime; however, our estimates have wide intervals, and it should be noted that viruses with G gene nucleotide sequences nearly identical to those of the original Canadian ON1 viruses were co-circulating with the diversified viruses at least up to late in 2012.
Our RSV ON1 genotype analyses were limited to the G ectodomain region (≈700 nt), and analyses for the global data were limited to the G C-terminus region (≈330 nt). Whole-genome comparison of 2 ON1 sequences currently available in GenBank (accession nos. JX627336/2011  and KC731482/2011 ) showed up to 57 nt differences, a substantial proportion of which occurred beyond the G protein gene region (data not shown). Thus, to better understand the local and global molecular epidemiology and phylogeography of the ON1 genotype, whole-genome sequences must be compared. To that end, we are currently conducting whole-genome sequencing of the ON1 viruses from Kilifi.
The phylodynamics of these emergent RSV genotypes with large nucleotide duplications in the G gene (i.e., the BA and ON1) enable parallels to be drawn with pandemic influenza viruses arising from antigenic shift. The cause of the apparent enhanced biologic fitness of the BA and ON1 genotypes (whether virologic or immunologic) is not well understood. Since around 2005, the BA genotype has dominated all other group B genotypes. We cannot tell if the ON1 genotype will also eventually dominate other group A genotypes. However, during the preparation of this report, the detection of RSV genotype ON1 was reported in 3 more countries: Thailand (33), Latvia (34), and Cyprus (35). Thus the prevalence and geographic distribution of ON1 is rapidly changing. The monitoring of this change will lead to a better understanding of the factors underlying the successful emergence of variant genotypes and help inform future methods for the control of RSV.
Mr Agoti is a research assistant in the Viral Epidemiology and Control group, Kenya Medical Research Institute–Wellcome Trust Research Programme, and a PhD student. His primary interest is to inform epidemic control strategies by applying phylogenetic and bioinformatics tools to understand the evolution and origins of respiratory viruses and relationships between viral epidemics.
We thank the parents and guardians of children participating in the study. We also thank the clinical and laboratory staff of the Kilifi Viral Epidemiology and Control group who obtained and processed the study specimens. The study is published with permission of director of the Kenya Medical Research Institute.
This work was supported by the Wellcome Trust (grant no. 084633).
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Suggested citation for this article: Agoti CN, Otieno JR, Gitahi CW, Cane PA, Nokes DJ. Rapid spread and diversification of respiratory syncytial virus genotype ON1, Kenya. Emerg Infect Dis. 2014 June [date cited]. http://dx.doi.org/10.3201/eid2006.131438
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