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Brazilian Journal of Medical and Biological Research

On-line version ISSN 1414-431X

Braz J Med Biol Res vol.34 no.4 Ribeirão Preto Apr. 2001

http://dx.doi.org/10.1590/S0100-879X2001000400005 

Braz J Med Biol Res, April 2001, Volume 34(4) 471-473 (Short Communication)

Genotyping of group A rotavirus samples from Brazilian children by probe hybridization

D.D.P. Cardoso1, M.L. Rácz3, M.S.P. Azevedo1, R.M.B. Martins1 and C.M.A. Soares2

1Laboratório de Virologia, Instituto de Patologia Tropical e Saúde Pública, and 2Laboratório de Biologia Molecular, Instituto de Ciências Biológicas, Universidade Federal de Goiás, Goiânia, GO, Brasil
3Laboratório de Virologia, Instituto de Ciências Biológicas, Universidade de São Paulo, São Paulo, SP, Brasil

Abstract
Text
References
Acknowledgments
Correspondence and Footnotes


Abstract

The G genotyping of 74 group A rotavirus samples was done by RNA-DNA hybridization (dot-blot) using oligonucleotide probes for the VP7 gene region of the human rotavirus serotypes/genotypes 1, 2, 3 and 4. Thirty-one samples could be genotyped by dot-blot showing the following results: G1 = 16, G4 = 6, G3 = 5, and G2 = 4. The data show circulation of genotypes G1-G4 and the predominance of G1. The knowledge of genotypes provides important information concerning rotavirus circulation in Central Brazil.

Key words: rotavirus, G genotyping, VP7, oligonucleotides


Human rotaviruses are recognized as the main agents of diarrhea of infants and young children and constitute an important cause of mortality in developing countries. The knowledge of the relative frequency and distribution of rotavirus serotypes/genotypes can help in the analysis of regional differences and variations over the years in population samples (1). The G serotypes/genotypes can be analyzed by several techniques (2-6), including enzyme immunoassay with monoclonal antibodies (EIA-mAb) (7,8). This is the main technique, although it is not able to define all serotypes. It has been proposed that the failure in serotyping by EIA-mAb could be due, for example, to the loss of VP7 (7,9). Nucleic acid hybridization techniques can be used to determine genotypes since the viral double-stranded RNA (dsRNA) is more resistant to degradation than the VP7 protein (10).

The present study describes the data obtained from G genotyping of rotavirus samples collected from children in Goiânia, GO, Brazil, using the RNA-DNA hybridization technique. We studied 2,158 samples from children up to 10 years of age, with or without diarrhea disease, collected from hospitals, outpatient clinics and day-care centers from March 1986 to June 1995. All fecal samples were previously tested by EIA for group A rotavirus using commercial kits (EIARA, Biomanguinhos, FIOCRUZ, Rio de Janeiro, RJ, Brazil) and RNA polyacrylamide gel electrophoresis (PAGE) (11,12). Two hundred and fifty-four samples were positive for group A rotavirus. Of the 254 rotavirus samples, 233 (91.7%) were from children with diarrhea. It should be pointed out that 226 (95.8%) were hospitalized children. In addition, regarding age, 220 of the 254 positive children were up to two years old. Seventy-four of the positive samples were genotyped by the hybridization technique (dot-blot). Probes complementary to nucleotides 315-339 of the VP7 gene from the human rotavirus serotypes/genotypes 1, 2, 3, and 4 were synthesized as described by Sethabutr et al. (10). The primers were labeled with [g32P]-ATP according to Sambrook et al. (13). dsRNA was extracted from the samples as described by Pereira et al. (11). Briefly, fecal samples were suspended in 1X PBS, pH 7.4 (0.14 M NaCl, 0.02 M KCl, 0.08 M Na2HPO4, 0.01 M KH2PO4), extracted with phenol-chloroform and precipitated with ethanol. Hybridization was performed by the method of Sethabutr et al. (10). Briefly, dsRNA was supplemented with the same volume of 20X SSC (20X SSC = 3 M NaCl plus 0.3 M sodium citrate)/37% formaldehyde (3 parts of SSC and 2 parts of formaldehyde) and heated at 65oC for 15 min. The denatured dsRNA was spotted on nitrocellulose membranes in a total volume of 25 µl. The membranes were heated for 2 h at 80oC and pre-hybridized in a solution containing 50% formamide, 1 mg/µl salmon DNA, 50% Denhardt's solution (Ficoll/polyvinylpyrrolidone/bovine serum albumin), and 1 M sodium phosphate buffer. The pre-hybridization and hybridization temperatures were 38oC for genotypes with 2 and 3 oligonucleotides and 42oC for genotypes with 1 and 4 oligonucleotides. Pre-hybridization was carried out for 4 h, followed by hybridization for 18 h in the same solution with 0.1% SDS and the labeled oligonucleotide added. The membranes were washed three times with solution containing 5X SSC and 0.1% SDS at room temperature, dried and exposed to an X-ray film for 24 h at -70oC.

Genotyping was considered positive when the signal for one genotype was unique or significantly higher than for the other genotypes (at least two times the intensity). Samples that presented the same signal intensity for more than one genotype were considered undetermined. The prototypes Wa (G1), SA-11 (G3) and ST-3 (G4) were used as positive controls. We also used one sample (9800) characterized by EIA-mAb as a positive control of genotype G2.

Table 1 shows the results of genotyping. Of 74 samples analyzed, 31 (41.9%) were assigned to genotypes G1 to G4 by dot-blot. Indices from 52.9 to 91.1% were described for genotyping using molecular techniques (10,14,15). Thirty-four samples (45.9%) were not genotyped by dot-blot analysis. The presence of dsRNA was observed by PAGE in 33 of 34 dot-blot-negative samples (data not shown), a fact excluding the possibility of the failure of genotyping being related to the absence of dsRNA, as suggested by Bingnan et al. (1). Negative results could be related to the failure of hybridization with the oligonucleotides due to the presence of other VP7 genes not included in this investigation, as well as mutation in the analyzed region (14,16,17). Bingnan et al. (1), in Bangladesh, observed a higher genotyping index (66.7%) using three additional oligonucleotides for other rotavirus genotypes. This result supports the suggestion of the occurrence of samples other than G1-G4 among the samples analyzed. In agreement, other serotypes have been described. The G5 serotype that infects mainly swine has been detected in Brazil (18,19). Oligonucleotides complementary to other VP7 regions, as well as oligonucleotides for other rotavirus serotypes should be useful to answer this question. Nine samples hybridized with more than one oligonucleotide probe. The significance of this result will be the subject of a future study. Our data support the need for continuous monitoring of rotavirus serotypes/genotypes at different times in different world regions.


References

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Acknowledgments

The authors would like to thank Adriana Crispim Azevedo for helpful technical assistance.


Correspondence and Footnotes

Address for correspondence: D.D.P. Cardoso, IPTSP/UFG, Rua Delenda Rezende Melo, Esquina com 1ª Avenida, Setor Universitário, 74605-050 Goiânia, GO, Brasil. Fax: +55-62-202-3066. E-mail: divina@netgo.com.br

Research supported by CNPq (No. 800149-89/0) and Fundação de Apoio à Pesquisa-FUNAPE/ PRPPG/UFG. Publication supported by FAPESP. Received July 25, 2000. Accepted February 5, 2001.

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