Open-access Characterization of rotavirus strains from day care centers: pre- and post-rotavirus vaccine era

Abstracts

OBJECTIVES: In 2006 the rotavirus vaccine was included in the Brazilian Immunization Program. The aim of this study was to report the results of a 5-year surveillance study of rotavirus strains in children < 5 years with acute gastroenteritis from day care centers in the state of São Paulo, Brazil. METHODS: This retrospective study was conducted with 30 day care centers from 2004 to 2008 with convenient surveillance fecal specimens, investigated by ELISA, SDS-PAGE, RT-PCR and gene sequencing to genotype characterization. RESULTS: Rotavirus infection was detected in 28.3% of samples (38/134). The most frequent genotypes detected were G9P[8] and G1P[8] in 2004; G1P[8] in 2005; GNTP[NT] in 2006; G2P[4] in 2007; and there were no cases in 2008. Mixed infections were not observed. Detection rate declined from 65.7% (23/35) in 2004 to 50% (9/18) in 2007. CONCLUSIONS: Genotype distribution varied according to collection year, accompanied by a reduction in detection rate. Use of rotavirus vaccine requires implementation of post-marketing surveillance to monitor rotavirus strain diversity and its efficacy against possible new emerging genotypes.

Rotavirus; day care centers; gastroenteritis


OBJETIVOS: Em 2006, a vacina contra rotavírus foi incluída no Programa Nacional de Imunização. Este estudo teve como objetivo analisar os resultados da vigilância de genótipos de rotavírus em crianças < 5 anos com gastrenterites agudas provenientes de creches no estado de São Paulo por um período de 5 anos. MÉTODOS: Este estudo retrospectivo foi realizado em 30 creches no período de 2004 a 2008, com amostras fecais convenientes da vigilância das diarreias agudas, analisadas por ELISA, SDS-PAGE, RT-PCR e sequenciamento genético para caracterização do genótipo. RESULTADOS: Infecções por rotavírus foram detectadas em 28,3% de amostras (38/134). Os genótipos mais frequentes detectados foram: G9P[8] e G1P[8] em 2004; G1P[8] em 2005; GNTP[NT] em 2006; G2P[4] em 2007; e nenhum caso foi relatado em 2008. Infecções mistas não foram observadas. A taxa de detecção diminuiu de 65,7% (23/35) em 2004 para 50% (9/18) em 2007. CONCLUSÕES: A distribuição do genótipo variou de acordo com os anos, acompanhada pela redução no número de casos detectados. É necessário intensificar a vigilância pós-implantação da vacina contra rotavírus, visando monitorar as linhagens circulantes e sua eficácia contra possíveis genótipos emergentes.

Rotavírus; creches; gastroenterites


ORIGINAL ARTICLE

Characterization of rotavirus strains from day care centers: pre- and post-rotavirus vaccine era

Simone G. MorilloI;Adriana LuchsI;Audrey CilliII;Fernanda F. CostaII;Rita de Cassia C. CarmonaI;Maria do Carmo S. T. TimenetskyIII

IMsc. Instituto Adolfo Lutz, Enteric Virus Laboratory, São Paulo, SP, Brazil

IIInstituto Adolfo Lutz, Enteric Virus Laboratory, São Paulo, SP, Brazil

IIIPhD. Instituto Adolfo Lutz, Enteric Virus Laboratory, São Paulo, SP, Brazil

ABSTRACT

OBJECTIVES: In 2006 the rotavirus vaccine was included in the Brazilian Immunization Program. The aim of this study was to report the results of a 5-year surveillance study of rotavirus strains in children < 5 years with acute gastroenteritis from day care centers in the state of São Paulo, Brazil.

METHODS: This retrospective study was conducted with 30 day care centers from 2004 to 2008 with convenient surveillance fecal specimens, investigated by ELISA, SDS-PAGE, RT-PCR and gene sequencing to genotype characterization.

RESULTS: Rotavirus infection was detected in 28.3% of samples (38/134). The most frequent genotypes detected were G9P[8] and G1P[8] in 2004; G1P[8] in 2005; GNTP[NT] in 2006; G2P[4] in 2007; and there were no cases in 2008. Mixed infections were not observed. Detection rate declined from 65.7% (23/35) in 2004 to 50% (9/18) in 2007.

CONCLUSIONS: Genotype distribution varied according to collection year, accompanied by a reduction in detection rate. Use of rotavirus vaccine requires implementation of post-marketing surveillance to monitor rotavirus strain diversity and its efficacy against possible new emerging genotypes.

Keywords: Rotavirus, day care centers, gastroenteritis.

Introduction

Viral pathogens are the most common causes of gastroenteritis in communities and other settings, including semi-closed institutions and hospitals.1 In infancy, group A rotavirus (RVA) are considered to be the most important etiological agent of acute non-bacterial gastroenteritis, including outbreaks and sporadic cases, independent of improvements in basic sanitation and hygiene procedures.2 RVA are the major etiologic agent of acute diarrhea in children, responsible for more than 600,000 deaths each year,3 in addition to the significant economic burden of RVA disease.4

In 2006 an attenuated G1P[8] vaccine was included in the Brazilian Immunization Program, preventing severe rotavirus gastroenteritis, and inducing significant reduction in the frequency of RVA detection in children with gastroenteritis.5 In fact, the RIX4414 vaccine efficacy was evaluated by Araujo et al.,6 showing 53.9 to 81.5% of protection against severe cases, and 81.2 to 93.0% of protection against hospitalization due to rotavirus gastroenteritis in children.

Recently, a high prevalence of G2P[4] was reported in Brazil and linked with this vaccination,7 suggesting that this monovalent vaccine possibly created conditions in which G2P[4] could acquire selective advantage over P[8] genotypes. More detailed investigations concerning the heterological protection conferred by rotavirus monovalent vaccine are key points to understand its immunogenic behavior.6,8

The aim of this study was to report the results of a 5-year surveillance study of rotavirus strains in children < 5 years with acute gastroenteritis from day care center in the state of São Paulo, Brazil, and to evaluate detection trends.

Methods

This retrospective study was conducted with 30 day care centers from 2004 to 2008 with convenient surveillance specimens collected from children under 5 years presenting acute gastroenteritis. Stool samples from patients with acute gastroenteritis were sent to the Enteric Virus Laboratory of Instituto Adolfo Lutz (IAL), a regional reference center for rotavirus surveillance and a member of the Acute Diarrheic Disease Monitoring Program (ADDMP). This program aims at early detection of diarrhea outbreaks with national extent, and has been previously approved by the Ethics Committee.

The samples studied were part of ADDMP, obtained from a convenient retrospective sampling, without inclusion or exclusion criteria, with no characterization of the participating day care centers; therefore, the study may not be representative of the actual epidemiological scenario. A molecular characterization of rotavirus genotypes pre- and post-Rotarix® vaccination was performed. It did not include clinical evaluation, so the study does not allow evaluation of security, immunogenicity or protection provided by vaccination.

A total of 134 fecal samples were tested for RVA using a commercial immunoenzymatic assay (PremierTM Rotaclone®, Meridian Bioscience Inc., USA), performed according to the manufacturer's instructions, and polyacrylamide gel electrophoresis (PAGE). Rotavirus-positive stools samples were typed after reverse transcription followed by nested PCR and sequencing with BigDyeTM on an ABI 377 (Applied Biosystems Inc., USA), analyzed with DNASTAR software.

Results

Rotavirus infection was detected in 28.3% (38∕134), and all samples belonged to group A, based on the migration pattern on PAGE. Genotype distribution showed a different profile for each year: 28.5% G9P[8] (10/35), 14.2% G1P[8] (5/35) and 20% GNTP[NT] (7/35) in 2004; 5.4% G1P[8] (2/37) in 2005; 9% GNTP[NT] (4/44) in 2006; 11.1% G2P[4] (2/8) and 38.8% GNTP[NT] (7/18) in 2007. Mixed infections were not observed. Detection rate declined from 65.7% (23/35) in 2004 to 50% (9/18) in 2007, with no cases in 2008 (Table 1).

The relationship between the VP7 sequences of seven G9 strains (R792, R840, R848, R863, R865, R866, R869), one G1 strain (R788), and a representative strain of the G9 genotype (Mc345) and G1 genotype (Wa) was shown as a distance tree constructed using the Clustal method. Comparison of the G9 sequences showed 94.9% similarity when compared to Mc345 and 95.6 to 99.8% of similarity among them. Comparison of the G1 sequence showed 90.3% similarity when compared to Wa.

Discussion

Our data show the presence of RVA G9P[8], G2P[4], and G1P[8] in agreement with the reported worldwide prevalence of these three genotypes.9 As expected, G9 was the most frequent genotype circulating during 2004. This genotype has been previously detected in Brazil, in agreement with global emergence.10,11 G1 was the second most common G type found, corresponding to the results of numerous studies focusing RVA G type distribution in many countries, including Brazil.9,11

The G2P[4] genotype was the only strain observed during 2007. Alternatively to the proposition that the RIX4414 vaccine created conditions in which G2P[4] could have acquired selective advantage, a temporal periodicity, within ~ 10-year cyclic pattern of G2P[4] has been observed in Brazil,11 and should be considered as an alternative explanation to the increased detection of this genotype since 2006. Although such periodicity could be related to RVA vaccine introduction,11 G2P[4] genotype was also the most prevalent RVA type detected during 2007 in northwest Portugal, a population naïve for RVA vaccine.12 Therefore, at least in some settings, this prevalence cannot be explained by the introduction of vaccination and may reflect normal fluctuation of co-circulation RVA genotypes, which is in line with reports from other countries and areas, in non-vaccinated population, showing exactly the same,13 including South America.14

Non-typeable RVA strains have been reported in almost every epidemiological survey around the world, regardless of the methodology employed. In our study, during 2006 any RVA positive samples from day care centers could be genotyped by multiplex RT-PCR, whereas almost all RVA positive samples of ADDMP from others settings showed G2P[4] specificity. Not only for epidemiological rotavirus strain surveillance but also for effective rotavirus vaccine development, there is a need for sensitive and reliable diagnostic techniques, such as the oligonucleotide microarray hybridization method.15 Combining the sensitivity of PCR and the specificity of hybridization, it successfully detects and unambiguously identifies such G genotypes.

As for pre- and post-vaccination periods, the changes in genotype distribution found are accompanied by a reduction in the detection rate of RVA from day care center samples sent to IAL starting with 65.7% (23/35) in 2004 toward to 50% (9/18) in 2007, and no cases in 2008. In fact, this reduction was observed in the number of general RVA outbreaks in the state of São Paulo from 35 (10,481 cases) in 2004; 24 (3,144 cases) in 2005; 35 (2,084 cases) in 2006; eight (164 cases) in 2007; to one (three cases) in 2008.16 On the other hand, analyses of RVA outbreaks of previous year's surveillances17 suggest a more variable pattern, with a natural fluctuation of RVA cases.

As for other vaccines, implementation of post-marketing surveillance is recommended, especially because diverse RVA strains co-circulate in the human population. It is important not only to monitor RVA diversity, but also its efficacy, since new emerging genotypes may not share capsid antigen with the vaccine virus. More studies concerning the ecology of rotavirus infections will be important to better understand whether the reduction in RVA detection rate observed in the past few years is a direct consequence of the vaccine implementation or only a cycle pattern.

References

References

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  • Correspondence
  • Publication Dates

    • Publication in this collection
      30 Apr 2010
    • Date of issue
      Apr 2010

    History

    • Accepted
      23 Dec 2009
    • Received
      21 Sept 2009
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