Skip to main content
Top
Published in: BMC Pediatrics 1/2019

Open Access 01-12-2019 | Vaccination | Research article

The evolving epidemiology of rotavirus A infection in Brazil a decade after the introduction of universal vaccination with Rotarix®

Authors: Filipe A. Carvalho-Costa, Rosane M. S. de Assis, Alexandre M. Fialho, Irene T. Araújo, Marcelle F. Silva, Mariela M. Gómez, Juliana S. Andrade, Tatiana L. Rose, Tulio M. Fumian, Eduardo M. Volotão, Marize P. Miagostovich, José Paulo G. Leite

Published in: BMC Pediatrics | Issue 1/2019

Login to get access

Abstract

Background

Brazil introduced the monovalent rotavirus vaccine (Rotarix®) in 2006. This study aimed to assess the epidemiology and genotype distribution of species-A rotavirus (RVA) in Brazil, comparing the pre- and post-vaccination periods.

Methods

Laboratory-based RVA surveillance included 866 municipalities in 22 Brazilian states, over a 21-year period. A total of 16,185 children with diarrheal diseases (DD) aged up to 12 years between 1996 and 2005 (pre-vaccination period, n = 7030) and from 2006 to 2017 (post-vaccination period, n = 9155) were enrolled. RVA was detected using ELISA immune assay and/or polyacrylamide gel electrophoresis and genotyped using nested PCR and/or nucleotide sequencing. RVA-positivity and genotypes detection rates were compared in distinct periods and age groups and Rotarix vaccination status.

Results

RVA-positivity in pre- and post-vaccination periods was, respectively: 4–11 months bracket, 33.3% (668/2006) and 16.3% (415/2547) (p <  0.001); 12–24 months, 28.2% (607/2154) and 22.2% (680/3068) (p <  0.001); 25–48 months, 17.4% (215/1235) and 29.4% (505/1720) (p <  0.001). Genotypes distribution in the pre- and post-vaccination periods was, respectively: G1P [8]/G1P[Not Typed], 417/855 (48.8%) and 118/1835 (6.4%) (p <  0.001); G2P [4]/G2P[NT], 47/855 (5.5%) and 838/1835 (45.7%) (p <  0.001); G3P [8]/G3P[NT], 55/855 (6.4%) and 253/1835 (13.8%) (p <  0.001); G9P [8]/G9P[NT], 238/855 (27.8%) and 152/1835 (8.3%) (p <  0.001); G12P [8]/G129P[NT], 0/871 (0%) and 249/1835(13.6%) (p <  0.001). Concerning infants aged 4–11 months, RVA frequency in fully vaccinated and non-vaccinated individuals was 11.9% (125/1052) and 24.5% (58/237) (p <  0.001), respectively. In children aged 12–24 months, RVA detection rate was 18.1% (253/1395) and 29.6% (77/260) (p <  0.001), for the vaccinated and non-vaccinated individuals, respectively (p <  0.001).

Conclusions

RVA infection was significantly less frequent in children aged ≤2 years with DD after implementing vaccination, mainly among vaccinated children. It was also observed a decrease of P [8] circulation and emergence of G2P[4] in 2005, and afterwards in the post-vaccine era, with spreading of G12P[8] in 2014–2015 and of G3P[8] in 2017. Continuous RVA surveillance must be carried out in this scenario.
Literature
1.
go back to reference Black RE, Cousens S, Johnson HL, Lawn JE, Rudan I, Bassani DG, et al. (child health epidemiology reference group of WHO and UNICEF). Global, regional, and national causes of child mortality in 2008: a systematic analysis. Lancet. 2010;375:969–1987.CrossRef Black RE, Cousens S, Johnson HL, Lawn JE, Rudan I, Bassani DG, et al. (child health epidemiology reference group of WHO and UNICEF). Global, regional, and national causes of child mortality in 2008: a systematic analysis. Lancet. 2010;375:969–1987.CrossRef
2.
go back to reference Wazny K, Zipursky A, Black R, Curtis V, Duggan C, Guerrant R, et al. Setting research priorities to reduce mortality and morbidity of childhood diarrhoeal disease in the next 15 years. PLoS Med. 2013;10:e1001446.CrossRef Wazny K, Zipursky A, Black R, Curtis V, Duggan C, Guerrant R, et al. Setting research priorities to reduce mortality and morbidity of childhood diarrhoeal disease in the next 15 years. PLoS Med. 2013;10:e1001446.CrossRef
3.
go back to reference Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, et al. (Child Health Epidemiology Reference Group of WHO and UNICEF). Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet 2012;379:2151–2161. Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, et al. (Child Health Epidemiology Reference Group of WHO and UNICEF). Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet 2012;379:2151–2161.
4.
go back to reference Mokdad AH, Forouzanfar MH, Daoud F, Mokdad AA, El Bcheraoui C, Moradi-Lakeh M, et al. Global and National Burden of diseases and injuries among children and adolescents between 1990 and 2013: findings from the global burden of disease 2013 study. JAMA Pediatr. 2016;170:267–87.CrossRef Mokdad AH, Forouzanfar MH, Daoud F, Mokdad AA, El Bcheraoui C, Moradi-Lakeh M, et al. Global and National Burden of diseases and injuries among children and adolescents between 1990 and 2013: findings from the global burden of disease 2013 study. JAMA Pediatr. 2016;170:267–87.CrossRef
5.
go back to reference Kotloff KL. The Burden and Etiology of Diarrheal Illness in Developing Countries. Pediatr Clin North Am. 2017;64:799–814. Kotloff KL. The Burden and Etiology of Diarrheal Illness in Developing Countries. Pediatr Clin North Am. 2017;64:799–814.
6.
go back to reference Kotloff KL, Nataro JP, Blackwelder WC, Nasrin D, Farag TH, Panchalingam S, et al. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the global enteric multicenter study, GEMS): a prospective, case-control study. Lancet. 2013;382:209–22.CrossRef Kotloff KL, Nataro JP, Blackwelder WC, Nasrin D, Farag TH, Panchalingam S, et al. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the global enteric multicenter study, GEMS): a prospective, case-control study. Lancet. 2013;382:209–22.CrossRef
7.
go back to reference Platts-Mills JA, Babji S, Bodhidatta L, Gratz J, Haque R, Havt A, et al. (MAL-ED Network investigators). Pathogen-specific burdens of community diarrhoea in developing countries: a multisite birth cohort study (MAL-ED). Lancet Glob Health. 2015;3:e564–75.CrossRef Platts-Mills JA, Babji S, Bodhidatta L, Gratz J, Haque R, Havt A, et al. (MAL-ED Network investigators). Pathogen-specific burdens of community diarrhoea in developing countries: a multisite birth cohort study (MAL-ED). Lancet Glob Health. 2015;3:e564–75.CrossRef
8.
go back to reference Lanata CF, et al. (child health epidemiology reference Group of the World Health Organization and UNICEF). Global causes of diarrheal disease mortality in children <5 years of age: a systematic review. PLoS One. 2013;8:e72788.CrossRef Lanata CF, et al. (child health epidemiology reference Group of the World Health Organization and UNICEF). Global causes of diarrheal disease mortality in children <5 years of age: a systematic review. PLoS One. 2013;8:e72788.CrossRef
9.
go back to reference Linhares AC, Stupka JA, Ciapponi A, Bardach AE, Glujovsky D, Aruj PK, et al. Burden and typing of rotavirus group A in Latin America and the Caribbean: systematic review and meta-analysis. Rev Med Virol. 2011;21:89–109.CrossRef Linhares AC, Stupka JA, Ciapponi A, Bardach AE, Glujovsky D, Aruj PK, et al. Burden and typing of rotavirus group A in Latin America and the Caribbean: systematic review and meta-analysis. Rev Med Virol. 2011;21:89–109.CrossRef
10.
go back to reference Operario DJ, Platts-Mills JA, Nadan S, Page N, Seheri M, Mphahlele J, et al. Etiology of severe acute watery diarrhea in children in the global rotavirus surveillance Network using quantitative polymerase chain reaction. J Infect Dis. 2017 Jul 15;216(2):220–7.CrossRef Operario DJ, Platts-Mills JA, Nadan S, Page N, Seheri M, Mphahlele J, et al. Etiology of severe acute watery diarrhea in children in the global rotavirus surveillance Network using quantitative polymerase chain reaction. J Infect Dis. 2017 Jul 15;216(2):220–7.CrossRef
11.
go back to reference Yu J, Lai S, Geng Q, Ye C, Zhang Z, Zheng Y, Wang L, Duan Z, Zhang J, Wu S, Parashar U, Yang W, Liao Q, Li Z. Prevalence of rotavirus and rapid changes in circulating rotavirus strains among children with acute diarrhea in China 2009–2015. J Infect. 2019;78:66–74. Yu J, Lai S, Geng Q, Ye C, Zhang Z, Zheng Y, Wang L, Duan Z, Zhang J, Wu S, Parashar U, Yang W, Liao Q, Li Z. Prevalence of rotavirus and rapid changes in circulating rotavirus strains among children with acute diarrhea in China 2009–2015. J Infect. 2019;78:66–74.
12.
go back to reference Gentsch JR, Laird AR, Bielfelt B, Griffin DD, Banyai K, Ramachandran M, et al. Serotype diversity and reassortment between human and animal rotavirus strains: implications for rotavirus vaccine programs. J Infect Dis. 2005;192(Suppl 1):S146–59.CrossRef Gentsch JR, Laird AR, Bielfelt B, Griffin DD, Banyai K, Ramachandran M, et al. Serotype diversity and reassortment between human and animal rotavirus strains: implications for rotavirus vaccine programs. J Infect Dis. 2005;192(Suppl 1):S146–59.CrossRef
13.
go back to reference Matthijnssens J, Ciarlet M, Heiman E, Arijs I, Delbeke T, McDonald SM, et al. Full genome-based classification of rotaviruses reveals a common origin between human Wa-like and porcine rotavirus strains and human DS-1-like and bovine rotavirus strains. J Virol. 2008;82:3204–19.CrossRef Matthijnssens J, Ciarlet M, Heiman E, Arijs I, Delbeke T, McDonald SM, et al. Full genome-based classification of rotaviruses reveals a common origin between human Wa-like and porcine rotavirus strains and human DS-1-like and bovine rotavirus strains. J Virol. 2008;82:3204–19.CrossRef
14.
go back to reference Matthijnssens J, Van Ranst M. Genotype constellation and evolution of group A rotaviruses infecting humans. Curr Opin Virol. 2012;2:426–33.CrossRef Matthijnssens J, Van Ranst M. Genotype constellation and evolution of group A rotaviruses infecting humans. Curr Opin Virol. 2012;2:426–33.CrossRef
15.
go back to reference World Health Organization. Rotavirus vaccines WHO position paper: January 2013 - recommendations. Vaccine. 2013;31:6170–1.CrossRef World Health Organization. Rotavirus vaccines WHO position paper: January 2013 - recommendations. Vaccine. 2013;31:6170–1.CrossRef
16.
go back to reference Tate JE, Burton AH, Boschi-Pinto C, Parashar UD. (World Health Organization–coordinated global rotavirus surveillance Network). Global, regional, and National Estimates of rotavirus mortality in children <5 years of age, 2000-2013. Clin Infect Dis. 2016;62(Suppl 2):S96–S105.CrossRef Tate JE, Burton AH, Boschi-Pinto C, Parashar UD. (World Health Organization–coordinated global rotavirus surveillance Network). Global, regional, and National Estimates of rotavirus mortality in children <5 years of age, 2000-2013. Clin Infect Dis. 2016;62(Suppl 2):S96–S105.CrossRef
17.
go back to reference Paternina-Caicedo A, Parashar UD, Alvis-Guzmán N, De Oliveira LH, Castaño-Zuluaga A, Cotes-Cantillo K, et al. Effect of rotavirus vaccine on childhood diarrhea mortality in five Latin American countries. Vaccine. 2015;33:3923–8.CrossRef Paternina-Caicedo A, Parashar UD, Alvis-Guzmán N, De Oliveira LH, Castaño-Zuluaga A, Cotes-Cantillo K, et al. Effect of rotavirus vaccine on childhood diarrhea mortality in five Latin American countries. Vaccine. 2015;33:3923–8.CrossRef
18.
go back to reference de Oliveira LH, Camacho LA, Coutinho ES, Ruiz-Matus C, Leite JP. Rotavirus vaccine effectiveness in Latin American and Caribbean countries: A systematic review and meta-analysis. Vaccine. 2015;33(Suppl 1):A248–54.CrossRef de Oliveira LH, Camacho LA, Coutinho ES, Ruiz-Matus C, Leite JP. Rotavirus vaccine effectiveness in Latin American and Caribbean countries: A systematic review and meta-analysis. Vaccine. 2015;33(Suppl 1):A248–54.CrossRef
19.
go back to reference Linhares AC, Velázquez FR, Pérez-Schael I, Sáez-Llorens X, Abate H, Espinoza FC, et al. (Human Rotavirus Vaccine Study Group 2008). Efficacy and safety of an oral live attenuated human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in Latin American infants: a randomized, double-blind, placebocontrolled phase III study. Lancet. 2008;371:1181–9.CrossRef Linhares AC, Velázquez FR, Pérez-Schael I, Sáez-Llorens X, Abate H, Espinoza FC, et al. (Human Rotavirus Vaccine Study Group 2008). Efficacy and safety of an oral live attenuated human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in Latin American infants: a randomized, double-blind, placebocontrolled phase III study. Lancet. 2008;371:1181–9.CrossRef
20.
go back to reference Ruiz-Palacios GM, Pérez-Schael I, Velázquez FR, Abate H, Breuer T, Clemens SC, et al. Human rotavirus vaccine study group 2006. Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. N Engl J Med. 2006;354:11–22.CrossRef Ruiz-Palacios GM, Pérez-Schael I, Velázquez FR, Abate H, Breuer T, Clemens SC, et al. Human rotavirus vaccine study group 2006. Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. N Engl J Med. 2006;354:11–22.CrossRef
21.
go back to reference Vesikari T, Karvonen A, Prymula R, Schuster V, Tejedor JC, Cohen R, et al. Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled study. Lancet. 2007;370:1757–63.CrossRef Vesikari T, Karvonen A, Prymula R, Schuster V, Tejedor JC, Cohen R, et al. Efficacy of human rotavirus vaccine against rotavirus gastroenteritis during the first 2 years of life in European infants: randomised, double-blind controlled study. Lancet. 2007;370:1757–63.CrossRef
23.
go back to reference Justino MC, Linhares AC, Lanzieri TM, Miranda Y, Mascarenhas JD, Abreu E, et al. Effectiveness of the monovalent G1P[8] human rotavirus vaccine against hospitalization for severe G2P[4] rotavirus gastroenteritis in Belém. Brazil Pediatr Infect Dis J. 2011;30:396–401.CrossRef Justino MC, Linhares AC, Lanzieri TM, Miranda Y, Mascarenhas JD, Abreu E, et al. Effectiveness of the monovalent G1P[8] human rotavirus vaccine against hospitalization for severe G2P[4] rotavirus gastroenteritis in Belém. Brazil Pediatr Infect Dis J. 2011;30:396–401.CrossRef
24.
go back to reference Ichihara MY, Rodrigues LC, Teles Santos CA, Teixeira Mda G, De Jesus SR, et al. Effectiveness of rotavirus vaccine against hospitalized rotavirus diarrhea: A case-control study. Vaccine. 2014;32:2740–7.CrossRef Ichihara MY, Rodrigues LC, Teles Santos CA, Teixeira Mda G, De Jesus SR, et al. Effectiveness of rotavirus vaccine against hospitalized rotavirus diarrhea: A case-control study. Vaccine. 2014;32:2740–7.CrossRef
25.
go back to reference Linhares AC, Justino MC. Rotavirus vaccination in Brazil: effectiveness and health impact seven years post-introduction. Expert Rev Vaccines. 2014;13:43–57.CrossRef Linhares AC, Justino MC. Rotavirus vaccination in Brazil: effectiveness and health impact seven years post-introduction. Expert Rev Vaccines. 2014;13:43–57.CrossRef
26.
go back to reference Desai R, Oliveira LH, Parashar UD, Lopman B, Tate JE, Patel MM. Reduction in morbidity and mortality from childhood diarrhoeal disease after species A rotavirus vaccine introduction in Latin America - a review. Mem Inst Oswaldo Cruz. 2011;106:907–11.CrossRef Desai R, Oliveira LH, Parashar UD, Lopman B, Tate JE, Patel MM. Reduction in morbidity and mortality from childhood diarrhoeal disease after species A rotavirus vaccine introduction in Latin America - a review. Mem Inst Oswaldo Cruz. 2011;106:907–11.CrossRef
27.
go back to reference Fernandes EG, Sato HK, Leshem E, Flannery B, Konstantyner TC, Veras MA, et al. Impact of rotavirus vaccination on diarrhea-related hospitalizations in São Paulo state, Brazil. Vaccine. 2014;32:3402–8.CrossRef Fernandes EG, Sato HK, Leshem E, Flannery B, Konstantyner TC, Veras MA, et al. Impact of rotavirus vaccination on diarrhea-related hospitalizations in São Paulo state, Brazil. Vaccine. 2014;32:3402–8.CrossRef
28.
go back to reference do Carmo GM, Yen C, Cortes J, Siqueira AA, de Oliveira WK, Cortez-Escalante JJ, et al. Decline in diarrhea mortality and admissions after routine childhood rotavirus immunization in Brazil: a time-series analysis. PLoS Med. 2011;8:e1001024.CrossRef do Carmo GM, Yen C, Cortes J, Siqueira AA, de Oliveira WK, Cortez-Escalante JJ, et al. Decline in diarrhea mortality and admissions after routine childhood rotavirus immunization in Brazil: a time-series analysis. PLoS Med. 2011;8:e1001024.CrossRef
29.
go back to reference Justino MC, Araújo EC, van Doorn LJ, Oliveira CS, Gabbay YB, Mascarenhas JD, et al. Oral live attenuated human rotavirus vaccine (Rotarix™) offers sustained high protection against severe G9P[8] rotavirus gastroenteritis during the first two years of life in Brazilian children. Mem Inst Oswaldo Cruz. 2012;107:846–53.CrossRef Justino MC, Araújo EC, van Doorn LJ, Oliveira CS, Gabbay YB, Mascarenhas JD, et al. Oral live attenuated human rotavirus vaccine (Rotarix™) offers sustained high protection against severe G9P[8] rotavirus gastroenteritis during the first two years of life in Brazilian children. Mem Inst Oswaldo Cruz. 2012;107:846–53.CrossRef
30.
go back to reference Hull JJ, Teel EN, Kerin TK, Freeman MM, Esona MD, Gentsch JR, et al. United States rotavirus strain surveillance from 2005 to 2008: genotype prevalence before and after vaccine introduction. Pediatr Infect Dis J. 2011;30(Suppl 1):S42–7.CrossRef Hull JJ, Teel EN, Kerin TK, Freeman MM, Esona MD, Gentsch JR, et al. United States rotavirus strain surveillance from 2005 to 2008: genotype prevalence before and after vaccine introduction. Pediatr Infect Dis J. 2011;30(Suppl 1):S42–7.CrossRef
31.
go back to reference Siqueira AA, Santelli AC, Alencar LR Jr, Dantas MP, Dimech CP, Carmo GM, et al. Outbreak of acute gastroenteritis in young children with death due to rotavirus genotype G9 in Rio Branco, Brazilian Amazon region, 2005. Int J Infect Dis. 2010;14:e898–903.CrossRef Siqueira AA, Santelli AC, Alencar LR Jr, Dantas MP, Dimech CP, Carmo GM, et al. Outbreak of acute gastroenteritis in young children with death due to rotavirus genotype G9 in Rio Branco, Brazilian Amazon region, 2005. Int J Infect Dis. 2010;14:e898–903.CrossRef
32.
go back to reference Pitzer VE, Patel MM, Lopman BA, Viboud C, Parashar UD, Grenfell BT, et al. Modeling rotavirus strain dynamics in developed countries to understand the potential impact of vaccination on genotype distributions. Proc Natl Acad Sci U S A. 2011;108:19353–8.CrossRef Pitzer VE, Patel MM, Lopman BA, Viboud C, Parashar UD, Grenfell BT, et al. Modeling rotavirus strain dynamics in developed countries to understand the potential impact of vaccination on genotype distributions. Proc Natl Acad Sci U S A. 2011;108:19353–8.CrossRef
33.
go back to reference Gómez MM, de Mendonça MC, Volotão Ede M, Tort LF, da Silva MF, Cristina J, et al. Rotavirus A genotype P[4]G2: genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009. J Med Virol. 2011;83:1093–6.CrossRef Gómez MM, de Mendonça MC, Volotão Ede M, Tort LF, da Silva MF, Cristina J, et al. Rotavirus A genotype P[4]G2: genetic diversity and reassortment events among strains circulating in Brazil between 2005 and 2009. J Med Virol. 2011;83:1093–6.CrossRef
34.
go back to reference Gómez MM, Carvalho-Costa FA, Volotão Ede M, Rose TL, da Silva MF, Fialho AM, et al. Prevalence and genomic characterization of G2P[4] group A rotavirus strains during monovalent vaccine introduction in Brazil. Infect Genet Evol. 2014;28:486–94.CrossRef Gómez MM, Carvalho-Costa FA, Volotão Ede M, Rose TL, da Silva MF, Fialho AM, et al. Prevalence and genomic characterization of G2P[4] group A rotavirus strains during monovalent vaccine introduction in Brazil. Infect Genet Evol. 2014;28:486–94.CrossRef
35.
go back to reference Patel MM, de Oliveira LH, Bispo AM, Gentsch J, Parashar UD, et al. Rotavirus P[4]G2 in a vaccinated population. Brazil Emerg Infect Dis. 2008;14:863–5.CrossRef Patel MM, de Oliveira LH, Bispo AM, Gentsch J, Parashar UD, et al. Rotavirus P[4]G2 in a vaccinated population. Brazil Emerg Infect Dis. 2008;14:863–5.CrossRef
36.
go back to reference Amarilla A, Espínola EE, Galeano ME, Fariña N, Russomando G, Parra GI, et al. Rotavirus infection in the Paraguayan population from 2004 to 2005: high incidence of rotavirus strains with short electropherotype in children and adults. Med Sci Monit. 2007;13:CR333–7.PubMed Amarilla A, Espínola EE, Galeano ME, Fariña N, Russomando G, Parra GI, et al. Rotavirus infection in the Paraguayan population from 2004 to 2005: high incidence of rotavirus strains with short electropherotype in children and adults. Med Sci Monit. 2007;13:CR333–7.PubMed
37.
go back to reference Mandile MG, Esteban LE, Argüelles MH, Mistchenko A, Glikmann G, Castello AA, et al. Surveillance of group A rotavirus in Buenos Aires 2008-2011, long last circulation of G2P[4] strains possibly linked to massive monovalent vaccination in the region. J Clin Virol. 2014;60:282–9.CrossRef Mandile MG, Esteban LE, Argüelles MH, Mistchenko A, Glikmann G, Castello AA, et al. Surveillance of group A rotavirus in Buenos Aires 2008-2011, long last circulation of G2P[4] strains possibly linked to massive monovalent vaccination in the region. J Clin Virol. 2014;60:282–9.CrossRef
38.
go back to reference Degiuseppe JI, Reale EA, Stupka JA. Argentine Rotavirus Surveillance Network. Rotavirus epidemiology and surveillance in Argentina: 2009-2011. Arch Argent Pediatr. 2013;111:148–54.CrossRef Degiuseppe JI, Reale EA, Stupka JA. Argentine Rotavirus Surveillance Network. Rotavirus epidemiology and surveillance in Argentina: 2009-2011. Arch Argent Pediatr. 2013;111:148–54.CrossRef
39.
go back to reference Kirkwood CD, Boniface K, Barnes GL, Bishop RF, et al. Distribution of rotavirus genotypes after introduction of rotavirus vaccines, Rotarix® and RotaTeq®, into the National Immunization Program of Australia. Pediatr Infect Dis J. 2011;30(Suppl 1):S48–53.CrossRef Kirkwood CD, Boniface K, Barnes GL, Bishop RF, et al. Distribution of rotavirus genotypes after introduction of rotavirus vaccines, Rotarix® and RotaTeq®, into the National Immunization Program of Australia. Pediatr Infect Dis J. 2011;30(Suppl 1):S48–53.CrossRef
40.
go back to reference da Silva SL, de Fátima Dos Santos GS, do Socorro Lima de Oliveira A, da Silva Dos Santos F, de Fátima Costa de Menezes EM, Mascarenhas J, et al. Diversity of rotavirus strains circulating in northern Brazil after introduction of a rotavirus vaccine: high prevalence of G3P[6] genotype. J Med Virol. 2014;86:1065–72.CrossRef da Silva SL, de Fátima Dos Santos GS, do Socorro Lima de Oliveira A, da Silva Dos Santos F, de Fátima Costa de Menezes EM, Mascarenhas J, et al. Diversity of rotavirus strains circulating in northern Brazil after introduction of a rotavirus vaccine: high prevalence of G3P[6] genotype. J Med Virol. 2014;86:1065–72.CrossRef
41.
go back to reference Luchs A, Cilli A, Morillo SG, Gregório Dde S, de Souza KA, Vieira HR, et al. Detection of the emerging rotavirus G12P[8] genotype at high frequency in Brazil in 2014: successive replacement of predominant strains after vaccine introduction. Acta Trop. 2016;156:87–94.CrossRef Luchs A, Cilli A, Morillo SG, Gregório Dde S, de Souza KA, Vieira HR, et al. Detection of the emerging rotavirus G12P[8] genotype at high frequency in Brazil in 2014: successive replacement of predominant strains after vaccine introduction. Acta Trop. 2016;156:87–94.CrossRef
42.
go back to reference Delogu R, et al. Unexpected spreading of G12P[8] rotavirus strains among young children in a small area of central Italy. J Med Virol. 2015;87:1292–302.CrossRef Delogu R, et al. Unexpected spreading of G12P[8] rotavirus strains among young children in a small area of central Italy. J Med Virol. 2015;87:1292–302.CrossRef
Metadata
Title
The evolving epidemiology of rotavirus A infection in Brazil a decade after the introduction of universal vaccination with Rotarix®
Authors
Filipe A. Carvalho-Costa
Rosane M. S. de Assis
Alexandre M. Fialho
Irene T. Araújo
Marcelle F. Silva
Mariela M. Gómez
Juliana S. Andrade
Tatiana L. Rose
Tulio M. Fumian
Eduardo M. Volotão
Marize P. Miagostovich
José Paulo G. Leite
Publication date
01-12-2019
Publisher
BioMed Central
Keyword
Vaccination
Published in
BMC Pediatrics / Issue 1/2019
Electronic ISSN: 1471-2431
DOI
https://doi.org/10.1186/s12887-019-1415-9

Other articles of this Issue 1/2019

BMC Pediatrics 1/2019 Go to the issue