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Published in: BMC Infectious Diseases 1/2020

01-12-2020 | Acute Gastroenteritis | Research article

Diversity of rotavirus genotypes circulating in children < 5 years of age hospitalized for acute gastroenteritis in India from 2005 to 2016: analysis of temporal and regional genotype variation

Authors: Sidhartha Giri, C. P. Girish Kumar, Shainey Alokit Khakha, Mamta Chawla-Sarkar, Varanasi Gopalkrishna, Shobha D. Chitambar, Pratima Ray, S. Venkatasubramanian, Biswa Jyoti Borkakoty, Subarna Roy, Jyothi Bhat, Bhagirathi Dwibedi, Pradeep Das, Vijayachari Paluru, Sasirekha Ramani, Sudhir Babji, Rashmi Arora, Sanjay M. Mehendale, Mohan D. Gupte, Gagandeep Kang, National Rotavirus Surveillance Network investigators

Published in: BMC Infectious Diseases | Issue 1/2020

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Abstract

Background

From 2016, the Government of India introduced the oral rotavirus vaccine into the national immunization schedule. Currently, two indigenously developed vaccines (ROTAVAC, Bharat Biotech; ROTASIIL, Serum Institute of India) are included in the Indian immunization program. We report the rotavirus disease burden and the diversity of rotavirus genotypes from 2005 to 2016 in a multi-centric surveillance study before the introduction of vaccines.

Methods

A total of 29,561 stool samples collected from 2005 to 2016 (7 sites during 2005–2009, 3 sites from 2009 to 2012, and 28 sites during 2012–2016) were included in the analysis. Stools were tested for rotavirus antigen using enzyme immunoassay (EIA). Genotyping was performed on 65.8% of the EIA positive samples using reverse transcription- polymerase chain reaction (RT-PCR) to identify the G (VP7) and P (VP4) types. Multinomial logistic regression was used to quantify the odds of detecting genotypes across the surveillance period and in particular age groups.

Results

Of the 29,561 samples tested, 10,959 (37.1%) were positive for rotavirus. There was a peak in rotavirus positivity during December to February across all sites. Of the 7215 genotyped samples, G1P[8] (38.7%) was the most common, followed by G2P[4] (12.3%), G9P[4] (5.8%), G12P[6] (4.2%), G9P[8] (4%), and G12P[8] (2.4%). Globally, G9P[4] and G12P[6] are less common genotypes, although these genotypes have been reported from India and few other countries. There was a variation in the geographic and temporal distribution of genotypes, and the emergence or re-emergence of new genotypes such as G3P[8] was seen. Over the surveillance period, there was a decline in the proportion of G2P[4], and an increase in the proportion of G9P[4]. A higher proportion of mixed and partially typed/untyped samples was also seen more in the age group 0–11 months.

Conclusions

This 11 years surveillance highlights the high burden of severe rotavirus gastroenteritis in Indian children < 5 years of age before inclusion of rotavirus vaccines in the national programme. Regional variations in rotavirus epidemiology were seen, including the emergence of G3P[8] in the latter part of the surveillance. Having pre-introduction data is important to track changing epidemiology of rotaviruses, particularly following vaccine introduction.
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Literature
1.
go back to reference Troeger C, Khalil IA, Rao PC, et al. Rotavirus vaccination and the global burden of rotavirus diarrhea among children younger than 5 years. JAMA Pediatr. 2018;172(10):958–65.PubMedPubMedCentralCrossRef Troeger C, Khalil IA, Rao PC, et al. Rotavirus vaccination and the global burden of rotavirus diarrhea among children younger than 5 years. JAMA Pediatr. 2018;172(10):958–65.PubMedPubMedCentralCrossRef
2.
go back to reference GBD 2016 Diarrhoeal Disease Collaborators. Estimates of the global, regional, and national morbidity, mortality, and aetiologies of diarrhoea in 195 countries: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Infect Dis. 2018;18:1211–28.CrossRef GBD 2016 Diarrhoeal Disease Collaborators. Estimates of the global, regional, and national morbidity, mortality, and aetiologies of diarrhoea in 195 countries: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Infect Dis. 2018;18:1211–28.CrossRef
3.
go back to reference John J, Sarkar R, Muliyil JBN, Bhan MK, Kang G. Rotavirus gastroenteritis in India, 2011-2013: revised estimates of disease burden and potential impact of vaccines. Vaccine. 2014;32S:A5–9.CrossRef John J, Sarkar R, Muliyil JBN, Bhan MK, Kang G. Rotavirus gastroenteritis in India, 2011-2013: revised estimates of disease burden and potential impact of vaccines. Vaccine. 2014;32S:A5–9.CrossRef
4.
go back to reference Kahn G, Fitzwater S, Tate J, et al. Epidemiology and prospects for prevention of rotavirus disease in India. Indian Pediatr. 2012;49:467–74.PubMedCrossRef Kahn G, Fitzwater S, Tate J, et al. Epidemiology and prospects for prevention of rotavirus disease in India. Indian Pediatr. 2012;49:467–74.PubMedCrossRef
5.
go back to reference Mishra V, Awasthi S, Nag VL, Tandon R. Genomic diversity of group a rotavirus strains in patients aged 1-36 months admitted for acute watery diarrhoea in northern India: a hospital-based study. Clin Microbiol Infect. 2010;16:45–50.PubMedCrossRef Mishra V, Awasthi S, Nag VL, Tandon R. Genomic diversity of group a rotavirus strains in patients aged 1-36 months admitted for acute watery diarrhoea in northern India: a hospital-based study. Clin Microbiol Infect. 2010;16:45–50.PubMedCrossRef
7.
go back to reference Mathew MA, Paulose A, Chitralekha S, Nair MKC, Kang G, Kilgore P. Prevalence of rotavirus diarrhea among hospitalized under-five children. Indian Pediatr. 2014;51:27–31.PubMedCrossRef Mathew MA, Paulose A, Chitralekha S, Nair MKC, Kang G, Kilgore P. Prevalence of rotavirus diarrhea among hospitalized under-five children. Indian Pediatr. 2014;51:27–31.PubMedCrossRef
8.
go back to reference Mullick S, Mandal P, Nayak MK, et al. Hospital based surveillance and genetic characterization of rotavirusstrains in children (<5 years) with acute gastroenteritis in Kolkata,India, revealed resurgence of G9 and G2 genotypes during 2011–2013. Vaccine. 2014;32S:A20–8.CrossRef Mullick S, Mandal P, Nayak MK, et al. Hospital based surveillance and genetic characterization of rotavirusstrains in children (<5 years) with acute gastroenteritis in Kolkata,India, revealed resurgence of G9 and G2 genotypes during 2011–2013. Vaccine. 2014;32S:A20–8.CrossRef
9.
go back to reference Tiku VR, Sharma S, Verma A, et al. Rotavirus diversity among diarrheal children in Delhi, India during 2007-2012. Vaccine. 2014;32S:A62–7.CrossRef Tiku VR, Sharma S, Verma A, et al. Rotavirus diversity among diarrheal children in Delhi, India during 2007-2012. Vaccine. 2014;32S:A62–7.CrossRef
10.
go back to reference Mukherjee A, Chattopadhyay S, Bagchi P, et al. Surveillance and molecular characterization of rotavirus strains circulating in Manipur, north-eastern India: increasing prevalence of emerging G12 strains. Infect Genet Evol. 2010;10:311–20.PubMedCrossRef Mukherjee A, Chattopadhyay S, Bagchi P, et al. Surveillance and molecular characterization of rotavirus strains circulating in Manipur, north-eastern India: increasing prevalence of emerging G12 strains. Infect Genet Evol. 2010;10:311–20.PubMedCrossRef
11.
go back to reference Chakravarti A, Chauhan MS, Sharma A, Verma V. Distribution of human rotavirus G and P genotypes in a hospital setting from northern India. Southeast Asian J Trop Med Public Health. 2010;41:1145–52.PubMed Chakravarti A, Chauhan MS, Sharma A, Verma V. Distribution of human rotavirus G and P genotypes in a hospital setting from northern India. Southeast Asian J Trop Med Public Health. 2010;41:1145–52.PubMed
12.
go back to reference Saluja T, Sharma SD, Gupta M, et al. A multicenter prospective hospital-based surveillance to estimatethe burden of rotavirus gastroenteritis in children less than five yearsof age in India. Vaccine. 2014;32S:A13–9.CrossRef Saluja T, Sharma SD, Gupta M, et al. A multicenter prospective hospital-based surveillance to estimatethe burden of rotavirus gastroenteritis in children less than five yearsof age in India. Vaccine. 2014;32S:A13–9.CrossRef
13.
go back to reference Bhandari N, Rongsen-Chandola T, Bavdekar A, et al. Efficacy of a monovalent human-bovine (116E) rotavirus vaccine in Indian infants: a randomised double blind placebo controlled trial. Lancet. 2014;383(9935):2136–43.PubMedPubMedCentralCrossRef Bhandari N, Rongsen-Chandola T, Bavdekar A, et al. Efficacy of a monovalent human-bovine (116E) rotavirus vaccine in Indian infants: a randomised double blind placebo controlled trial. Lancet. 2014;383(9935):2136–43.PubMedPubMedCentralCrossRef
14.
go back to reference Riddle MS, Chen WH, Kirkwood CD, MacLennan CA. Update on vaccines for enteric pathogens. Clin Microbiol Infect. 2018;24:1039–45.PubMedCrossRef Riddle MS, Chen WH, Kirkwood CD, MacLennan CA. Update on vaccines for enteric pathogens. Clin Microbiol Infect. 2018;24:1039–45.PubMedCrossRef
15.
go back to reference Kang G, Desai R, Arora R, et al. Diversity of circulating rotavirus strains in children hospitalized with diarrhea in India, 2005–2009. Vaccine. 2013;31(27):2879–83.PubMedCrossRef Kang G, Desai R, Arora R, et al. Diversity of circulating rotavirus strains in children hospitalized with diarrhea in India, 2005–2009. Vaccine. 2013;31(27):2879–83.PubMedCrossRef
16.
go back to reference Bresee J, Parashar U, Holman R, Gentsch J, Glass R. Generic protocols for (i) hospital-based surveillance to estimate the burden of rotavirus gastroenteritis in children and (ii) a community-based survey on utilization of health care services for gastroenteritis in children. Document WHO/V&B/02 15. Geneva: World Health Organization; 2002. p. 20021–67. Bresee J, Parashar U, Holman R, Gentsch J, Glass R. Generic protocols for (i) hospital-based surveillance to estimate the burden of rotavirus gastroenteritis in children and (ii) a community-based survey on utilization of health care services for gastroenteritis in children. Document WHO/V&B/02 15. Geneva: World Health Organization; 2002. p. 20021–67.
17.
go back to reference Babji S, Arumugam R, Saravanabhavan A, et al. Multi-center surveillance of rotavirus diarrhea in hospitalizedchildren <5 years of age in India, 2009–2012. Vaccine. 2014;32S:A10–2.CrossRef Babji S, Arumugam R, Saravanabhavan A, et al. Multi-center surveillance of rotavirus diarrhea in hospitalizedchildren <5 years of age in India, 2009–2012. Vaccine. 2014;32S:A10–2.CrossRef
18.
go back to reference Kang G, Arora R, Chitambar SD, et al. Multicenter, hospital-based surveillance of rotavirus disease and strains among Indian children aged <5 years. J Infect Dis. 2009;200:S147–53.PubMedCrossRef Kang G, Arora R, Chitambar SD, et al. Multicenter, hospital-based surveillance of rotavirus disease and strains among Indian children aged <5 years. J Infect Dis. 2009;200:S147–53.PubMedCrossRef
19.
go back to reference Iturriza-Gomara M, Green J, Brown DWG, Desselberger U, Gray JJ. Comparison of specific and random priming in the reverse transcriptase polymerase chain reaction for genotyping group a rotaviruses. J Virol Methods. 1999;78(1–2):93–103.PubMedCrossRef Iturriza-Gomara M, Green J, Brown DWG, Desselberger U, Gray JJ. Comparison of specific and random priming in the reverse transcriptase polymerase chain reaction for genotyping group a rotaviruses. J Virol Methods. 1999;78(1–2):93–103.PubMedCrossRef
20.
go back to reference Banerjee I, Ramani S, Primrose B, et al. Modification of rotavirus multiplex RT-PCR for the detection of G12 strains based on characterization of emerging G12 rotavirus strains from South India. J Med Virol. 2007;79(9):1413–21.PubMedPubMedCentralCrossRef Banerjee I, Ramani S, Primrose B, et al. Modification of rotavirus multiplex RT-PCR for the detection of G12 strains based on characterization of emerging G12 rotavirus strains from South India. J Med Virol. 2007;79(9):1413–21.PubMedPubMedCentralCrossRef
21.
go back to reference Babji S, Arumugam R, Sarvanabhavan A, Gentsch JR, Kang G. Approach to molecular characterization of partially and completely untyped samples in an Indian rotavirus surveillance program. Vaccine. 2014;32:A84–8.PubMedCrossRefPubMedCentral Babji S, Arumugam R, Sarvanabhavan A, Gentsch JR, Kang G. Approach to molecular characterization of partially and completely untyped samples in an Indian rotavirus surveillance program. Vaccine. 2014;32:A84–8.PubMedCrossRefPubMedCentral
22.
go back to reference Chawla-Sarkar M, Banerjee A, Lo M, et al. A decade long temporal analyses of human group-a rotavirus among children with gastroenteritis: Prevaccination scenario in West Bengal, eastern India. J Med Virol. 2020;92:1334–42. Chawla-Sarkar M, Banerjee A, Lo M, et al. A decade long temporal analyses of human group-a rotavirus among children with gastroenteritis: Prevaccination scenario in West Bengal, eastern India. J Med Virol. 2020;92:1334–42.
23.
go back to reference Babji S, Arumugam R, Priyahemavathy R, et al. Genotype distribution of group a rotavirus from southern India, 2005-2016. Vaccine. 2018;36(51):7816–9.PubMedCrossRef Babji S, Arumugam R, Priyahemavathy R, et al. Genotype distribution of group a rotavirus from southern India, 2005-2016. Vaccine. 2018;36(51):7816–9.PubMedCrossRef
24.
go back to reference Kelkar SD, Purohit SG, Boralkar AN, Verma SP. Prevalence of rotavirus diarrhoea among hospitalized children in Pune, India. Indian J Med Res. 2001;109:131–5. Kelkar SD, Purohit SG, Boralkar AN, Verma SP. Prevalence of rotavirus diarrhoea among hospitalized children in Pune, India. Indian J Med Res. 2001;109:131–5.
25.
go back to reference Saravanan P, Ananthan S, Ananthasubramanian M. Rotavirus infection among infants and young children in Chennai, South India. Indian J Med Microbiol. 2004;22:212–21.PubMed Saravanan P, Ananthan S, Ananthasubramanian M. Rotavirus infection among infants and young children in Chennai, South India. Indian J Med Microbiol. 2004;22:212–21.PubMed
26.
go back to reference Nair GB, Ramamurthy T, Bhattacharya MK, et al. Emerging trends in the etiology of enteric pathogens as evidenced from an active surveillance of hospitalized diarrhoeal patients in Kolkata, India. Gut Pathog. 2010;2:4.PubMedPubMedCentralCrossRef Nair GB, Ramamurthy T, Bhattacharya MK, et al. Emerging trends in the etiology of enteric pathogens as evidenced from an active surveillance of hospitalized diarrhoeal patients in Kolkata, India. Gut Pathog. 2010;2:4.PubMedPubMedCentralCrossRef
27.
go back to reference Van Damme P, Giaquinto C, Huet F, Gothefors L, Maxwell M, Van der Wielen M. Multicenter prospective study of the burden of rotavirus acute gastroenteritis in Europe, 2004-2005: the REVEAL study. J Infect Dis. 2007;195:S4–16.PubMedCrossRef Van Damme P, Giaquinto C, Huet F, Gothefors L, Maxwell M, Van der Wielen M. Multicenter prospective study of the burden of rotavirus acute gastroenteritis in Europe, 2004-2005: the REVEAL study. J Infect Dis. 2007;195:S4–16.PubMedCrossRef
28.
go back to reference Santos VS, Marques DP, Martins-Filho PRS, Cuevas LE, Gurgel RQ. Effectiveness of rotavirus vaccines against rotavirus infection and hospitalization in Latin America: systematic review and metaanalysis. Infect Dis Poverty. 2016;5:83.PubMedPubMedCentralCrossRef Santos VS, Marques DP, Martins-Filho PRS, Cuevas LE, Gurgel RQ. Effectiveness of rotavirus vaccines against rotavirus infection and hospitalization in Latin America: systematic review and metaanalysis. Infect Dis Poverty. 2016;5:83.PubMedPubMedCentralCrossRef
29.
go back to reference Hallowell BD, Parashar UD, Curns A, DeGroote NP, Tate JE. Trends in the Laboratory Detection of Rotavirus Before and After Implementation of Routine Rotavirus Vaccination-United States, 2000–2018. MMWR Morb Mortal Wkly Rep. 2019;68(24):539–43. Hallowell BD, Parashar UD, Curns A, DeGroote NP, Tate JE. Trends in the Laboratory Detection of Rotavirus Before and After Implementation of Routine Rotavirus Vaccination-United States, 2000–2018. MMWR Morb Mortal Wkly Rep. 2019;68(24):539–43.
30.
go back to reference Santos N, Hoshino Y. Global distribution of rotavirus serotypes/genotypes and its implication for the development and implementation of an effective rotavirus vaccine. Rev Med Virol. 2005;15:29–56.PubMedCrossRef Santos N, Hoshino Y. Global distribution of rotavirus serotypes/genotypes and its implication for the development and implementation of an effective rotavirus vaccine. Rev Med Virol. 2005;15:29–56.PubMedCrossRef
31.
go back to reference Taniguchi K, Urasawa T, Kobayashi M, Gorziglia M, Urasawa S. Nucleotide sequence of VP4 and VP7 genes of human rotaviruses with subgroup I specificity and long RNA pattern: implication for new G serotype specificity. J Virol. 1990;64:5640–4.PubMedPubMedCentralCrossRef Taniguchi K, Urasawa T, Kobayashi M, Gorziglia M, Urasawa S. Nucleotide sequence of VP4 and VP7 genes of human rotaviruses with subgroup I specificity and long RNA pattern: implication for new G serotype specificity. J Virol. 1990;64:5640–4.PubMedPubMedCentralCrossRef
32.
go back to reference Rahman M, Matthijnssens J, Yang X, et al. Evolutionary history and global spread of the emerging G12 human rotaviruses. J Virol. 2007;81(5):2382–90.PubMedCrossRef Rahman M, Matthijnssens J, Yang X, et al. Evolutionary history and global spread of the emerging G12 human rotaviruses. J Virol. 2007;81(5):2382–90.PubMedCrossRef
33.
go back to reference Das S, Varghese V, Chaudhury S, Barman P, Mahapatra S, Kojima K. Emergence of novel human group a rotavirus G12 strains in India. J Clin Microbiol. 2003;41(6):2760–2.PubMedPubMedCentralCrossRef Das S, Varghese V, Chaudhury S, Barman P, Mahapatra S, Kojima K. Emergence of novel human group a rotavirus G12 strains in India. J Clin Microbiol. 2003;41(6):2760–2.PubMedPubMedCentralCrossRef
34.
go back to reference Sharma S, Ray P, Gentsch JR, Glass RI, Kalra V, Bhan MK. Emergence of G12 rotavirus strains in Delhi, India, in 2000 to 2007. J Clin Microbiol. 2008;46(4):1343–8.PubMedPubMedCentralCrossRef Sharma S, Ray P, Gentsch JR, Glass RI, Kalra V, Bhan MK. Emergence of G12 rotavirus strains in Delhi, India, in 2000 to 2007. J Clin Microbiol. 2008;46(4):1343–8.PubMedPubMedCentralCrossRef
36.
go back to reference Ansari S, Sherchand JB, Rijal BP, et al. Characterization of rotavirus causing acute diarrhoea in children in Kathmandu, Nepal, showing the dominance of serotype G12. J Med Microbiol. 2013;62:114–20.PubMedCrossRef Ansari S, Sherchand JB, Rijal BP, et al. Characterization of rotavirus causing acute diarrhoea in children in Kathmandu, Nepal, showing the dominance of serotype G12. J Med Microbiol. 2013;62:114–20.PubMedCrossRef
37.
go back to reference Sherchand JB, Nakagomi O, Dove W, et al. Molecular epidemiology of rotavirus diarrhea among children aged <5 years in Nepal: predominance of emergent G12 strains during 2 years. J Infect Dis. 2009;200:S182–7.PubMedCrossRef Sherchand JB, Nakagomi O, Dove W, et al. Molecular epidemiology of rotavirus diarrhea among children aged <5 years in Nepal: predominance of emergent G12 strains during 2 years. J Infect Dis. 2009;200:S182–7.PubMedCrossRef
38.
go back to reference Uchida R, Pandey BD, Sherchand JB, et al. Molecular epidemiology of rotavirus diarrhea among children and adults in Nepal: detection of G12 strains with P [6] or P [8] and a G11P[25] strain. J Clin Microbiol. 2006;44(10):3499–505.PubMedPubMedCentralCrossRef Uchida R, Pandey BD, Sherchand JB, et al. Molecular epidemiology of rotavirus diarrhea among children and adults in Nepal: detection of G12 strains with P [6] or P [8] and a G11P[25] strain. J Clin Microbiol. 2006;44(10):3499–505.PubMedPubMedCentralCrossRef
39.
go back to reference Ide T, Higo-Moriguchi K, Komoto S, et al. High prevalence of G12 human rotaviruses in children with gastroenteritis in Myanmar. Jpn J Infect Dis. 2016;69:326–7.PubMedCrossRef Ide T, Higo-Moriguchi K, Komoto S, et al. High prevalence of G12 human rotaviruses in children with gastroenteritis in Myanmar. Jpn J Infect Dis. 2016;69:326–7.PubMedCrossRef
41.
go back to reference Moe K, Thu HM, Oo WM, et al. Genotyping of rotavirus isolates collected from children less than 5 years of age admitted for diarrhoea at the Yangon Children's hospital, Myanmar. Vaccine. 2009;27S:F89–92.CrossRef Moe K, Thu HM, Oo WM, et al. Genotyping of rotavirus isolates collected from children less than 5 years of age admitted for diarrhoea at the Yangon Children's hospital, Myanmar. Vaccine. 2009;27S:F89–92.CrossRef
42.
go back to reference Ahmed K, Batuwanthudawe R, Nilmini Chandrasena TGA, et al. Rotavirus infections with multiple emerging genotypes in Sri Lanka. Arch Virol. 2010;155:71–5.PubMedCrossRef Ahmed K, Batuwanthudawe R, Nilmini Chandrasena TGA, et al. Rotavirus infections with multiple emerging genotypes in Sri Lanka. Arch Virol. 2010;155:71–5.PubMedCrossRef
44.
go back to reference Bucardo F, Mercado J, Reyes Y, Gonzalez F, Balmaseda A, Nordgren J. Large increase of rotavirus diarrhoea in the hospital setting associated with emergence of G12 genotype in a highly vaccinated population in Nicaragua. Clin Microbiol Infect. 2015;21:603 e1–603.e7.PubMedCrossRef Bucardo F, Mercado J, Reyes Y, Gonzalez F, Balmaseda A, Nordgren J. Large increase of rotavirus diarrhoea in the hospital setting associated with emergence of G12 genotype in a highly vaccinated population in Nicaragua. Clin Microbiol Infect. 2015;21:603 e1–603.e7.PubMedCrossRef
45.
go back to reference Das BK, Gentsch JR, Cicirello HG, et al. Characterization of rotavirus strains from newborns in New Delhi, India. J Clin Microbiol. 1994;32(7):1820–2.PubMedPubMedCentralCrossRef Das BK, Gentsch JR, Cicirello HG, et al. Characterization of rotavirus strains from newborns in New Delhi, India. J Clin Microbiol. 1994;32(7):1820–2.PubMedPubMedCentralCrossRef
47.
go back to reference Ghosh S, Varghese V, Samajdar S, Bhattacharya SK, Kobayashi N, Naik TN. Molecular characterization of a porcine group a rotavirus strain with G12 genotype specificity. Arch Virol. 2006;151(7):1329–44.PubMedCrossRef Ghosh S, Varghese V, Samajdar S, Bhattacharya SK, Kobayashi N, Naik TN. Molecular characterization of a porcine group a rotavirus strain with G12 genotype specificity. Arch Virol. 2006;151(7):1329–44.PubMedCrossRef
48.
go back to reference Hoshino Y, Honma S, Jones RW, Ross J, Santos N, Gentsch JR. A porcine G9 rotavirus strain shares neutralization and VP7 phylogenetic sequence lineage 3 characteristics with contemporary human G9 rotavirus strains. Virology. 2005;332(1):177–88.PubMedCrossRef Hoshino Y, Honma S, Jones RW, Ross J, Santos N, Gentsch JR. A porcine G9 rotavirus strain shares neutralization and VP7 phylogenetic sequence lineage 3 characteristics with contemporary human G9 rotavirus strains. Virology. 2005;332(1):177–88.PubMedCrossRef
49.
go back to reference Teodoroff TA, Tsunemitsu H, Okamoto K, et al. Predominance of porcine rotavirus G9 in Japanese piglets with diarrhea: close relationship of their VP7 genes with those of recent human G9 strains. J Clin Microbiol. 2005;43(3):1377–84.PubMedPubMedCentralCrossRef Teodoroff TA, Tsunemitsu H, Okamoto K, et al. Predominance of porcine rotavirus G9 in Japanese piglets with diarrhea: close relationship of their VP7 genes with those of recent human G9 strains. J Clin Microbiol. 2005;43(3):1377–84.PubMedPubMedCentralCrossRef
50.
go back to reference Hungerford D, Vivancos R, EuroRotaNet network members, et al. In-season and out-of-season variation of rotavirus genotype distribution and age of infection across 12 European countries before the introduction of routine vaccination, 2007/08 to 2012/13. Euro Surveill. 2016;21(2):1–12.CrossRef Hungerford D, Vivancos R, EuroRotaNet network members, et al. In-season and out-of-season variation of rotavirus genotype distribution and age of infection across 12 European countries before the introduction of routine vaccination, 2007/08 to 2012/13. Euro Surveill. 2016;21(2):1–12.CrossRef
Metadata
Title
Diversity of rotavirus genotypes circulating in children < 5 years of age hospitalized for acute gastroenteritis in India from 2005 to 2016: analysis of temporal and regional genotype variation
Authors
Sidhartha Giri
C. P. Girish Kumar
Shainey Alokit Khakha
Mamta Chawla-Sarkar
Varanasi Gopalkrishna
Shobha D. Chitambar
Pratima Ray
S. Venkatasubramanian
Biswa Jyoti Borkakoty
Subarna Roy
Jyothi Bhat
Bhagirathi Dwibedi
Pradeep Das
Vijayachari Paluru
Sasirekha Ramani
Sudhir Babji
Rashmi Arora
Sanjay M. Mehendale
Mohan D. Gupte
Gagandeep Kang
National Rotavirus Surveillance Network investigators
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2020
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-020-05448-y

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