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Published on: July 22, 2012
Rotavirus serotypes and electropherotypes identified among hospitalised children in São Luís, Maranhão, Brazil
Cláudia Regina N E da Luz1, Joana D'Arc P Mascarenhas, Yvone B Gabbay
1Hospital Universitário Materno Infantil, Universidade Federal do Maranhão, São Luís, Maranhão, Brazil.
Insights
Rotavirus infections cause severe infantile gastroenteritis in Northeastern Brazil. A future vaccine should protect against multiple rotavirus serotypes, particularly G1 and G2, to be effective.
Area of Science:
- Virology
- Pediatrics
- Public Health
Background:
- Rotavirus is a leading cause of severe infantile gastroenteritis globally.
- Understanding local rotavirus epidemiology is crucial for vaccine development and public health strategies.
- Northeastern Brazil has a high burden of diarrheal diseases in infants.
Purpose of the Study:
- To investigate the prevalence and characteristics of rotavirus infections in hospitalized infants with acute diarrhea.
- To determine the electropherotypes and G serotypes of rotavirus strains circulating in Northeastern Brazil.
- To assess the seasonality and age distribution of rotavirus gastroenteritis in the study population.
Main Methods:
- Stool samples were collected from infants (≤2 years) hospitalized with acute diarrhea and from age-matched controls without diarrhea.
- Rotavirus detection was performed using enzyme immunoassays.
- Electropherotyping and serotyping (G serotype) were conducted on positive samples to characterize circulating strains.
Main Results:
- Rotavirus was detected in 32.0% of diarrheic infants versus 9.8% of controls (p < 0.001).
- G1 serotype was the most prevalent (66.7%), followed by G2.
- Both long and short electropherotypes were observed; G1 strains showed both patterns, while G2 strains had short patterns.
- Rotavirus infections occurred year-round, peaking in the second half of 1998 and in infants aged 6-11 months.
- G1 serotypes emerged in June 1998, while G2 strains circulated throughout the study period.
Conclusions:
- Rotaviruses are a significant cause of severe infantile gastroenteritis in Northeastern Brazil.
- The circulation of multiple rotavirus strains, particularly G1 and G2, highlights the need for broad-spectrum vaccines.
- Findings support the development of rotavirus vaccines offering protection against diverse serotypes.
Abstract:
During June 1997-June 1999 rotavirus infection was screened in infants aged up to 2 years and hospitalised with acute diarrhoea in São Luís, Northeastern Brazil. Altogether, 128 stool samples were collected from diarrhoeic patients and additional 122 faecal specimens from age and temporal matched inpatients without diarrhoea were obtained; rotavirus positivity rates for these groups were 32.0% (41/128) and 9.8% (12/122), respectively (p < 0.001). Both electropherotyping and serotyping could be performed in 42 (79.2%) of the 53 rotavirus-positive stool samples. Long and short electropherotypes were detected at similar rates--38.1% and 40.5% of specimens, respectively. Overall, a G serotype could be assigned for 35 (83.3%) of specimens, the majority of them (66.7%) bearing G1-serotype specificity. Taking both electropherotypes and serotypes together, G1 rotavirus strains displaying long and short RNA patterns accounted for 30.9% and 19.0% of tested specimens, respectively; all G2 strains had short electropherotype. Rotavirus gastroenteritis was detected year-round and, in 1998, the incidence rates tended to be higher during the second semester than in the first semester: 45.2% and 26.1% (p = 0.13), respectively. Rotavirus infections peaked at the second semester of life with frequencies of 30.1% and 13.5% for diarrhoeic children and controls, respectively. While the six rotavirus strains bearing G2-type specificity were circulating throughout the whole study period, G1 serotypes (n = 27) emerged as from June 1998 onwards, 20 (74.1%) of which clustering in 1998. These data underscore the importance of rotaviruses in the aetiology of severe infantile gastroenteritis in Northeastern Brazil and sustain the concept that a future vaccine should confer protection against more than one serotype.
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