Volume 25, Number 9—September 2019
Vaccine Effectiveness against DS-1–Like Rotavirus Strains in Infants with Acute Gastroenteritis, Malawi, 2013–2015
Atypical DS-1–like G1P rotaviruses emerged in 2013 in Malawi after rotavirus vaccine introduction. Vaccine effectiveness among infants hospitalized with acute DS-1–like G1P rotavirus gastroenteritis was 85.6% (95% CI 34.4%–96.8%). These findings suggest that vaccine provides protection against these strains despite their emergence coinciding with vaccine introduction.
Rotavirus remains a major cause of severe dehydration, diarrhea, and death among children <5 years of age in many low-income countries. After the introduction of Rotarix (Glaxo SmithKline, https://www.gsksource.com) rotavirus vaccine into Malawi’s immunization schedule in October 2012, enhanced surveillance combined with case–control studies have described the substantial population impact and effectiveness of Rotarix on hospitalized rotavirus disease and diarrheal deaths (1,2).
Both of the globally available rotavirus vaccines, Rotarix and RotaTeq (Merck & Co., https://www.merckvaccines.com), have been shown to protect against rotaviruses with a broad range of G and P types, as defined by the 2 viral outer-capsid proteins (3,4). A whole-genome classification system describes rotavirus strains more completely by assigning genotypes to each of its 11 double-stranded RNA segments (5). Most rotavirus strains contain either a Wa (G1-P-I1-R1-C1-M1-A1-N1-T1-E1-H1) or DS-1 (G2-P-I2-R2-C2-M2-A2-N2-T2-E2-H2) genotype constellation (6). Typically, G1P strains, including the Rotarix strain (RIX4414), possess a Wa-like genetic backbone, whereas G2P strains generally have a DS-1–like genotype constellation (6). A switch in predominant rotavirus genotype from G1P to G2P after Rotarix introduction has been described in various settings (7,8), and higher vaccine effectiveness (VE) against G1P strains has been described compared with G2P in some settings (2,9). It is not known whether these changes in strain distribution and strain-specific differences in VE are related to differences in cross-protection afforded by the outer capsid proteins (G and P type) or to the distinct genetic backbones possessed by DS-1–like strains and the Wa-like Rotarix strain.
Previously, we demonstrated that all G1P strains detected before Rotarix introduction in Malawi had a Wa-like genetic backbone (10). Shortly after Rotarix introduction, atypical DS-1–like G1P rotavirus strains were detected, which provided an opportunity to examine whether emergence of DS-1–like G1P strains could be the result of reduced protection afforded by the Wa-like G1P Rotarix vaccine.
We used enzyme immunoassay (EIA) to detect rotaviruses in stool samples collected from children <5 years of age with acute gastroenteritis at Queen Elisabeth Central Hospital (QECH; Blantyre, Malawi) (2). We used reverse transcription PCR to assign G and P genotypes to rotavirus-positive samples (10,11). Samples with sufficient volume and containing G1 (n = 110), G2 (n = 64), or other (G4, G9, or G12, n = 42) rotavirus strains were selected at random during January 2013–December 2015.
We generated rotavirus whole-genome sequences (WGS) using the HiSeq 2000 platform (Illumina Inc., https://www.illumina.com) as described previously (10). We derived consensus sequences using Geneious (https://www.geneious.com) and genotyped them using RotaC (http://rotac.regatools.be). All complete nucleotide sequences generated in this study were deposited into GenBank (12) (accession nos. MG181227–941).
We calculated rotavirus VE using logistic regression to compare 2-dose versus 0-dose vaccination status among hospitalized strain-specific rotavirus diarrhea case-patients and concurrently hospitalized control patients with non–rotavirus-caused diarrhea, matched by age at admission. We defined concurrency of controls for each endpoint (Table) as any patient hospitalized for diarrhea who tested negative for rotavirus occurring in the same date range (between the first and last hospitalized strain-specific case) in which cases of strain-specific rotavirus were detected. We limited VE analysis to infants <12 months of age because previous analysis did not demonstrate statistically significant protection in the second year of life (VE 31.7%, 95% CI −140.6% to 80.6%) (2). We obtained ethics approval from the National Health Sciences Research Committee, Malawi (867), and the Research Ethics Committee of the University of Liverpool, Liverpool, UK (000490).
Of 216 rotavirus strains sequenced, 114 (53%) had a Wa-like and 88 (44%) a DS-1–like genotype constellation. Among Wa-like strains, 72% were G1, <1% were G2, and 25% were G12. Of the DS-1–like strains, 31% were G1 and 69% were G2. Of the 110 G1 strains analyzed by WGS, 75% were Wa-like and 25% were DS-1–like. We detected atypical G1 rotaviruses with DS-1–like genotype constellation in Malawi in 2013; their circulation peaked in 2014 and subsequently decreased in 2015 (<1%, 1/72) (Figure).
In logistic regression analysis adjusted for year of presentation, Rotarix effectiveness against DS-1–like G1P rotavirus was 85.6% (95% CI 34.4%–96.8%; p = 0.01). Effectiveness estimates against Wa-like G1 (VE 76.7%, 95% CI −153.8% to 97.9%) and DS-1–like G2 (VE 48.5%, 95% CI −154.3% to 89.6%) rotaviruses included wide bounds and the null value (Table).
Atypical DS-1–like G1 rotavirus strains emerged in Malawi shortly after Rotarix vaccine introduction (10). Although strain oscillation and emergence of novel types have been reported globally in the absence of vaccination, the mechanisms driving this phenomenon are not well understood. It is possible that the emergence of these DS-1–like G1P strains was coincidental with vaccine introduction. The high VE strongly suggests that escape from vaccine-induced immunity is not the driver for emergence. The swift decline in prevalence of these strains is in contrast with more sustained changes in strain circulation described in other settings in the context of high VE (13). The decline could have been precipitated by the observed high VE or may represent a natural phenomenon related to viral fitness and associated periodic nature of the circulation of the DS-1–like strains, which has been observed historically and globally in the absence of vaccine. These findings support continued use of rotavirus vaccine in this population as an intervention to reduce severe diarrhea caused by rotavirus strains possessing either Wa-like or DS-1–like genetic backbones. The observed decline in rotavirus hospitalizations in children after vaccine introduction (2), together with reduction in infant diarrhea deaths in Malawi (14), are public health benefits that could be sustained through rotavirus vaccination in this region, which has one of the highest burdens of rotavirus disease.
The VE against DS-1–like G1P strains in this study resembles our previous findings of VE of 82% (95% CI 42%–95%) against all G1P strains 3 years after vaccine introduction (2013–2015) (2). In contrast, we were unable to demonstrate statistically significant VE against DS-1–like G2 rotaviruses despite a comparable number of such strains, consistent with our earlier study (VE 45.9%, 95% CI −47.0% to 80.1%; p = 0.228) (2). The apparently lower VE against rotavirus disease caused by DS-1–like strains associated with G2, but not with G1P, lends support to the proposed dominant role of the outer capsid proteins VP7 and VP4 as drivers of homotypic protection. Although increasing evidence suggests that Rotarix vaccine does not provide the same degree of protection against G2 strains as G1 strains, this difference in protection appears to have little effect on total VE among populations in which vaccination performs optimally and high VE is maintained. However, the difference in protection between the strains may exacerbate underperformance of rotavirus vaccines in low-resource settings such as Malawi, where overall VE is generally lower for reasons that remain poorly understood (2,15).
We could not demonstrate statistically significant effectiveness against Wa-like G1P rotaviruses (p = 0.23). Wa-like G1P cases became dominant and replaced DS-1–like G1P once vaccine coverage had reached high and stable levels (Figure). At high population vaccine coverage, case–control analysis of VE became challenging and difficult to power sufficiently.
Our data demonstrate that Rotarix provides a high degree of protection against severe disease caused by homotypic G1P rotaviruses in Malawi regardless of genomic backbone. VE for patients <1 year of age is comparable to that seen in middle-income countries. The lower VE against heterotypic G2P strains previously described (15) suggests that more detailed immune response studies, clarification of the correlates of protection for rotavirus disease, and strain surveillance are needed to monitor the impact of sustained, high vaccine coverage on rotavirus strain distribution.
Dr. Jere is a Wellcome International Training Fellow who conducted this research as part of his postdoctoral studies. His research interests are in enteric viral pathogens.
We thank the laboratory staff at the Malawi-Liverpool-Wellcome Trust Clinical Research Programme and the sequencing and informatics teams at the Centre for Genomic Research (CGR), University of Liverpool, UK.
This work was supported by an investigator-initiated research grant from GlaxoSmithKline Biologicals SA (eTrack no. 207219) and by the Wellcome Trust (Programme grant no. 091909/Z/10/Z and the MLW Programme Core Award). K.C.J. is a Wellcome Trust Training Fellow (grant no. 201945/Z/16/Z). M.I.-G. is partly supported by the NIHR HPRU in Gastrointestinal Infections.
Author contributions: K.C.J., N.B.-Z., N.A.C., and M.I.-G. conceived and designed the study. K.C.J. and N.B.-Z. collected clinical data and stool samples. K.C.J. performed the laboratory work. K.C.J. and N.B.-Z. carried out the statistical analyses. K.C.J. drafted the manuscript, with major input from N.A.C. and M.I.-G. All authors contributed to interpretation of the data and commented on the manuscript. All authors have read and approved the final manuscript.
Disclaimer: The funders had no role in the study design, data collection and interpretation, or the decision to submit the work for publication. GlaxoSmithKline Biologicals SA was provided the opportunity to review a preliminary version of this manuscript for factual accuracy, but the authors are solely responsible for final content and interpretation. The authors received no financial support or other form of compensation related to the development of the manuscript.
M. I.-G. is affiliated with the National Institute for Health Research Health Protection Research Unit in Gastrointestinal Infections at University of Liverpool in partnership with Public Health England, in collaboration with University of East Anglia, University of Oxford, and the Quadram Institute. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, the Department of Health or Public Health, England.
Potential conflicts of interest: K.C.J., N.B.-Z. and N.F. have received investigator-initiated research grant support from the GSK group of companies. M.I.-G. has received investigator-initiated research grant support from the GSK group of companies and Sanofi Pasteur Merck Sharpe & Dohme and Merck. O.N. has received research grant support and honoraria from Japan Vaccine and MSD for delivering lectures on rotavirus vaccines. N.A.C. has received research grant support and honoraria for participation in rotavirus vaccine data safety monitoring committee meetings from the GSK group of companies. All other authors report no potential conflicts.
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TableCite This Article
Original Publication Date: July 30, 2019
1These authors contributed equally to this article.
Table of Contents – Volume 25, Number 9—September 2019
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Khuzwayo C. Jere, University of Liverpool, Institute of Infection and Global Health, Ronald Ross Bldg, 8 West Derby St, Liverpool, L69 7BE, UK