Previous Article | Next Article 
Journal of Clinical Microbiology, July 2003, p. 3399-3402, Vol. 41, No. 7
0095-1137/03/$08.00+0 DOI: 10.1128/JCM.41.7.3399-3402.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Surveillance of Rotavirus Strains in Rio de Janeiro, Brazil, from 1997 to 1999
Norma Santos,1* Caroline C. Soares,1 Eduardo M. Volotão,1 Maria Carolina M. Albuquerque,1 and Yasutaka Hoshino2
Departamento de Virologia, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro RJ 21.941-590, Brazil,1
Laboratory of Infectious Diseases, National Institutes of Health, Bethesda, Maryland 208922
Received 22 January 2003/
Returned for modification 4 March 2003/
Accepted 27 March 2003

ABSTRACT
One hundred fifty-seven (23%;
n = 678) rotavirus-positive stool
samples were collected between March 1997 and December 1999
in the cites of Rio de Janeiro and Niterói. Rotaviruses
in 143 (91%) samples were genotyped by reverse transcription-PCR
for G and/or P specificity. Rotaviruses in the majority of G-P-typeable
samples (73.3%; 74 of 101) were identified as having globally
common genotypes G1P[8], G2P[4], G3P[8], and G4P[8]. Unusual
strains such as G1P[9], G2[P8], G3P[9], and G9P[4] strains were
detected in 8.9% (9 of 101) of the samples. Genotypes G9P[8],
G9P[6], and a mixture of G9 and other G or P types represented
15.9% (25 of 157) of the isolates. Mixed infections were detected
in 25 (15.9%) samples, and rotaviruses in 15 samples (9.6%)
were not typed.

TEXT
Rotaviruses, which are members of the
Reoviridae family, are
classified into seven groups (rotaviruses A to G). A complete
virus particle possesses 11 double-stranded RNA segments surrounded
by three concentric protein layers. Since their first detection
3 decades ago, group A rotaviruses have been established as
the major cause of severe acute gastroenteritis in infants and
young children in both developed and developing countries and
are estimated to cause 800,000 or more deaths annually among
children <5 years of age in the developing countries (
22).
The development of a safe and effective rotavirus vaccine has
thus been a global public health goal. Extensive epidemiological
studies worldwide have demonstrated that genotypes G1P[8], G2P[4],
G3P[8], and G4P[8] are responsible for the majority of rotavirus
infections (
13,
32). Thus, most of the candidate rotavirus vaccines
developed so far are designed to cover G and/or P serotypes
of epidemiologic importance (
22). Recently, rotaviruses bearing
G9P[8] or G9P[6] specificity have emerged as globally important
(
1,
2,
3,
5,
9,
18,
26,
29,
31,
33,
34,
38,
41,
42). There are
also indications that in Brazil rotavirus genotype G5P[8] may
be of epidemiologic importance (
17).
Since 1996 we have been conducting an epidemiological rotavirus strain surveillance in Rio de Janeiro, Brazil, to monitor the distribution and evolution of the rotavirus genotypes (e.g., the emergence of unusual or new rotavirus genotypes) circulating in the community. During the first year of surveillance we detected a high prevalence rate of genotype G5 in the two largest cities in Rio de Janeiro State (Rio de Janeiro and Niterói) (36). We present here the follow-up data of the rotavirus strain surveillance in Rio de Janeiro and Niterói from 1997 to 1999.
One hundred fifty-seven (23%, n = 678) rotavirus-positive stool samples from children under 5 years of age with acute diarrhea were collected between March 1997 and December 1999 in the cities of Rio de Janeiro and Niterói. The presence of rotavirus in those samples was determined by polyacrylamide gel electrophoresis analysis. Fifty-two rotavirus strains that could not be typed directly from stool samples, possibly due to inhibitors present in the sample, were adapted to growth in cell cultures of primary African green monkey kidney cells (BioWhittaker, Walkersville, Md.). Rotavirus double-stranded RNA was extracted from stool samples or infected-cell culture lysates and analyzed by reverse transcription-PCR for determination of rotavirus G and P specificity by using primers specific for genotypes G1 to G6, G8 to G11, P[4], P[6], P[8], P[9], and P[10] (10, 12, 14, 15, 21, 39).
G genotypes were successfully determined for 129 of 157 (82.2%) rotavirus-positive samples. Overall, G1 was the most prevalent (30%; 47 of 157), followed by G2 (14%; 22 of 157), G9 (12.1%; 19 of 157), G3 (10.2%; 16 of 157), and G4 (1.9%; 3 of 157). Rotavirus in 28 (17.8%) samples was nontypeable, and 22 (14%) specimens had mixed G genotype infections (Table 1). P genotypes were determined for 132 (84%) samples, and the P type distribution was as follows: P[8], 45.9% (72 of 157); P[4], 18.5% (29 of 157); P[9], 4.4% (7 of 157); P[6], 1.9% (3 of 157). Twenty-five (15.9%) samples were nontypeable, and 21 (13.4%) samples had mixed P genotype infections (Table 2).
View this table:
[in this window]
[in a new window]
|
TABLE 1. Human group A rotavirus G genotypes detected in the cities of Rio de Janeiro and Niterói, Brazil, from 1997 to 1999
|
View this table:
[in this window]
[in a new window]
|
TABLE 2. P genotypes of human group A rotavirus detected in the cities of Rio de Janeiro and Niterói, Brazil, from 1997 to 1999
|
Both G and P genotypes were determined for 101 of 157 (64.3%)
rotavirus strains. The most frequent G and P combination was
G1P[8] (39.6%; 40 of 101), followed by G2P[4] (20.8%; 21 of
101), G9P[8] (14.8%; 15 of 101), G3P[8] (9.9%; 10 of 101), G9P[6]
(3.0%; 3 of 101), and G4P[8] (3.0%; 3 of 101) (Table
3). Unusual
combinations such as G1P[9], G2[P8], and G9P[4] were observed
at low frequency (1%; one each), and G3P[9] strains represented
5.9% (6 of 101) of the isolates. Fifteen of 157 (9.6%) specimens
remained nontypeable for both G and P genotypes, and 16 of 157
(10.2%) specimens were typed for the G or P genotype only. Twenty-five
of 157 (15.9%) samples presented a mixture of G and/or P types
(Table
4).
View this table:
[in this window]
[in a new window]
|
TABLE 3. Human group A rotavirus G-P genotype combinations identified in the cities of Rio de Janeiro and Niterói during rotavirus seasons from 1997 to 1999
|
During the 3-year surveillance, 157 rotavirus strains were detected
and analyzed, and the majority of the specimens whose G and
P types were identified (73.3%; 74 of 101) had the globally
common genotypes G1P[8], G2P[4], G3P[8], and G4P[8]. Unexpectedly,
15.9% (25 of 157) of the strains were typed as either G9P[8],
G9P[6], G9P[4], or a mixture of G9 and other G or P types. Before
1997 in Brazil, a single G9 rotavirus strain was detected in
humans (
24) whereas two G9 strains were detected in diarrheal
piglets in 1991 (
37). In the present survey, only one G9 strain
was detected in 1997; however, the relative frequency of the
G9 genotype increased abruptly to 25% (9 of 36 strains) in 1998
and to 27.7% (15 of 54 strains) in 1999. It will be important
to monitor the evolution of the G9 genotype in this and other
regions of this country in coming years. Unusual strains such
as those with G1P[9], G2[P8], G3P[9], and G9P[4] genotypes represented
5.9% (9 of 101) of the isolates. That the G5 genotype was not
detected was particularly intriguing since this G genotype represented
57% of the isolates in 1996 (
17,
36). Whether its disappearance
is related to the emergence of the G9 genotype is unknown. However,
it is possible that the evolution of the rotavirus G5 genotype
in Brazil may resemble that of the rotavirus G9 genotype in
the United States, where it was initially detected in Philadelphia,
Pa., in 1983 to 1984 in 9.2% of infants with rotaviral disease
(
7) and then disappeared for about 1 decade. The G9 genotype
reemerged in the same city with an incidence of 56% in rotavirus
diarrhea in 1995 to 1996 (H. F. Clark, personal communication)
and at a lower frequency in other U.S. cities as well (
18,
34).
Surveillance of rotavirus genotype distribution has been conducted regularly in Brazil since 1982 (2, 6, 16, 19, 20, 23, 25, 27, 28, 35, 36, 38, 40). These studies were performed in various locations in the country and provided a rich database on rotavirus genotype distribution. Overall, the relative frequencies and distribution of rotavirus G and P genotypes in Brazil are similar to those of other countries, with genotypes G1, G2, G3, G4, P[8], and P[4] being the most prevalent. Nevertheless, other rotavirus genotypes have also been detected. Rotavirus genotype epidemiology in Brazil has been shown to have three characteristic features: (i) a great diversity of G and P genotypes circulating simultaneously; (ii) a frequent occurrence of unusual G and/or P genotypes as well as unusual G-P combinations, and (iii) a high proportion of mixed rotavirus infections, which appear to facilitate genetic reassortment between strains and the subsequent appearance of new G-P combinations.
For example, in 1994 Gouvea and colleagues first demonstrated the occurrence of rotavirus genotype G5 among Brazilian children with diarrhea in São Paulo (16). This G genotype was later shown to be widely distributed in the country, almost exclusively in association with the P[8] genotype (17). More recently, one single strain bearing G5P[6] genotype specificity has been described (28). The frequency of rotavirus type G5 infections increased progressively until 1996, when it was detected in 57% of rotavirus-positive fecal specimens analyzed in Rio de Janeiro (17, 36). After 1996, detection of the G5 strains decreased, showing that they undergo a periodic fluctuation in prevalence in a community, as has been described for G1 to G4 strains (4, 11, 29, 30). However, the circulation of G5 rotavirus among humans was shown to be restricted no longer to Brazil, as infections with such strains appeared in Argentina and Paraguay, suggesting a possible spread of these viruses across South America (4, 8). Interestingly, the decreased frequency of G5 strains coincided with the emergence of the rotavirus G9 genotype in Brazil (2, 35, 38). The genotype G9 strains were usually detected in combination with genotype P[8], although a few G9 strains bearing P[4] or P[6] specificity were also detected (2, 38). The frequency of rotavirus genotype G9 detection appears to be increasing throughout the world in the last few years, and G9 could be regarded as the fifth globally important genotype epidemiologically (1, 2, 3, 5, 9, 18, 26, 29, 31, 33, 34, 38, 41, 42). With regard to P genotypes in Brazil, even though P[8] and P[4] have been shown to be the most common P genotypes in the country, other P genotypes such as P[6] (often) and P[9] (less frequent) have also been detected among the Brazilian populations (2, 23, 38, 40). The need for continuous surveillance of rotavirus strains in communities in Brazil is emphasized.

ACKNOWLEDGMENTS
We thank Ronald Jones, Jerri Ross, and Mariam Wagner for their
expert technical assistance and Albert Kapikian for encouragement
throughout the study.
This work was partially supported by CNPq, FINEP, FAPERJ, FUJB, and CAPES, Brazil, and TWAS, Italy.

FOOTNOTES
* Corresponding author. Mailing address: Departamento de Virologia, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Cidade Universitária, CCS-Bl. I, Ilha do Fundão, Rio de Janeiro RJ 21.941-590, Brazil. Phone: 55 021 2260-9311. Fax: 55 021 2560-8344. E-mail:
nsantos{at}micro.ufrj.br.


REFERENCES
1 - Adah, M. I., A. Wade, and K. Taniguchi. 2001. Molecular epidemiology of rotaviruses in Nigeria: detection of unusual strains with G2P[6] and G8P[1] specificities. J. Clin. Microbiol. 39:3969-3975.[Abstract/Free Full Text]
2 - Araújo, I. T., M. S. R. Ferreira, A. M. Fialho, R. M. Assis, C. M. Cruz, M. Rocha, and J. P. G. Leite. 2001. Rotavirus genotypes P[4]G9, P[6]G9, and P[8]G9 in hospitalized children with acute gastroenteritis in Rio de Janeiro, Brazil. J. Clin. Microbiol. 39:1999-2001.[Abstract/Free Full Text]
3 - Bok, K., G. Palacios, K. Sijvarger, D. Matson, and J. Gomez. 2001. Emergence of G9P[6] human rotavirus in Argentina: phylogenetic relationships among G9 strains. J. Clin. Microbiol. 39:4020-4025.[Abstract/Free Full Text]
4 - Bok, K., N. Castagnaro, A. Borsa, S. Nates, C. Espul, O. Fay, A. Fabri, S. Grinstein, I. Miceli, D. O. Matson, and J. A. Gómez. 2001. Surveillance for rotavirus in Argentina. J. Med. Virol. 65:190-198.[CrossRef][Medline]
5 - Bon, F., C. Fromantin, S. Aho, P. Pothier, E. Kohli, and The Azay Group. 2000. G and P genotyping of rotavirus strains circulating in France over a three-year period: detection of G9 and P[6] strains at low frequencies. J. Clin. Microbiol. 38:1681-1683.[Abstract/Free Full Text]
6 - Cardoso, D. D. P., M. L. Rácz, M. S. P. Azevedo, R. M. B. Martins, and C. M. A. Soares. 2001. Genotyping of group A rotavirus samples from Brazilian children by probe hybridization. Braz. J. Med. Biol. Res. 34:471-473.[Medline]
7 - Clark, H. F., Y. Hoshino, L. M. Bell, J. Groff, G. Hess, P. Bachman, and P. A. Offit. 1987. Rotavirus isolates WI61 representing a presumptive new human serotype. J. Clin. Microbiol. 25:1757-1762.[Abstract/Free Full Text]
8 - Coluchi, N., V. Munford, J. Manzur, C. Vazquez, M. Escobar, E. Weber, P. Mármol, and M. L. Rácz. 2002. Detection, subgroup specificity, and genotype diversity of rotavirus strains in children with acute diarrhea in Paraguay. J. Clin. Microbiol. 40:1709-1714.[Abstract/Free Full Text]
9 - Cunliffe, N. A., J. S. Gondwe, R. L. Broadhead, M. E. Molyneux, P. A. Woods, J. S. Bresee, R. I. Glass, J. R. Gentsch, and C. A. Hart. 1999. Rotavirus G and P types in children with acute diarrhea in Blantyre, Malawi, from 1997 to 1998. J. Med. Virol. 57:308-312.[CrossRef][Medline]
10 - Das, B. K., J. R. Gentsch, H. G. Cicirello, P. A. Woods, A. Gupta, M. Ramachandran, R. Kumar, R. Bhan, M. K. Bhan, and R. I. Glass. 1994. Characterization of rotavirus strains from newborns in New Delhi, India. J. Clin. Microbiol. 32:1820-1822.[Abstract/Free Full Text]
11 - Das, S., A. Sen, G. Uma, V. Varghese, S. Chaudhuri, S. K. Bhattacharya, T. Krishnan, P. Dutta, D. Dutta, M. K. Bhattacharya, U. Mitra, N. Kobayashi, and T. N. Naik. 2002. Genomic diversity of group A rotavirus strains infecting humans in eastern India. J. Clin. Microbiol. 40:146-149.[Abstract/Free Full Text]
12 - Gentsch, J. R., R. I. Glass, P. Woods, V. Gouvea, M. Gorziglia, J. Flores, B. K. Das, and M. K. Bhan. 1992. Identification of group A rotavirus gene 4 types by polymerase chain reaction. J. Clin. Microbiol. 30:1365-1373.[Abstract/Free Full Text]
13 - Gentsch, J. R., P. A. Woods, M. Ramachandran, B. K. Das, J. P. G. Leite, A. Alfieri, R. Kumar, M. K. Bhan, and R. I. Glass. 1996. Review of G and P typing results from a global collection of rotavirus strains: implications for vaccine development. J. Infect. Dis. 174(Suppl.):S30-S36.
14 - Gouvea, V., R. I. Glass, P. A. Woods, K. Taniguchi, H. F. Clark, B. Forrester, and Z. Y. Fang. 1990. Polymerase chain reaction amplification and typing of rotavirus nucleic acid from stool specimens. J. Clin. Microbiol. 28:276-282.[Abstract/Free Full Text]
15 - Gouvea, V., N. Santos, and M. Timenetsky. 1994. Identification of bovine and porcine G types by PCR. J. Clin. Microbiol. 32:1338-1340.[Abstract/Free Full Text]
16 - Gouvea, V., L. de Castro, M. C. Timenetsky, H. Greenberg, and N. Santos. 1994. Rotavirus serotype G5 associated with diarrhea in Brazilian children. J. Clin. Microbiol. 32:1408-1409.[Abstract/Free Full Text]
17 - Gouvea, V., and N. Santos. 1999. Rotavirus serotype G5: an emerging cause of epidemic childhood diarrhea. Vaccine 17:1291-1292.[CrossRef][Medline]
18 - Griffin, D. D., C. D. Kirkwood, U. D. Parashar, P. A. Woods, J. S. Bresee, R. I. Glass, J. R. Gentsch, and The National Rotavirus Strain Surveillance System Collaborating Laboratories. 2000. Surveillance of rotavirus strains in the United States: identification of unusual strains. J. Clin. Microbiol. 38:2784-2787.[Abstract/Free Full Text]
19 - Gusmão, R. H. P., J. D. P. Mascarenhas, Y. B. Gabbay, Z. Lins-Lainson, F. L. P. Ramos, T. A. F. Monteiro, S. A. Valente, and A. C. Linhares. 1995. Rotaviruses as a cause of nosocomial, infantile diarrhoea in Northern Brazil: pilot study. Mem. Inst. Oswaldo Cruz 90:743-749.[Medline]
20 - Gusmão, R. H. P., J. D. P. Mascarenhas, Y. B. Gabbay, Z. Lins-Lainson, F. L. P. Ramos, T. A. F. Monteiro, A. S. Valente, U. Fagundes-Neto, and A. C. Linhares. 1999. Rotavirus subgroups, G serotypes, and electrophoretypes in cases of nosocomial infantile diarrhoea in Belém, Brazil. J. Trop. Pediatr. 45:81-86.[Abstract/Free Full Text]
21 - Isegawa, Y., O. Nakagomi, T. Nakagomi, S. Uesugi, and S. Ueda. 1993. Determination of bovine rotavirus G and P serotypes by polymerase chain reaction. Mol. Cell. Probes 7:277-284.[CrossRef][Medline]
22 - Kapikian, A. Z., Y. Hoshino, and R. M. Chanock. 2001. Rotaviruses, p. 1787-1825. In D. M. Knipe and R. M. Howley. (ed.), Fields virology, 4th ed., Lippincott, Williams & Wilkins, Philadelphia, Pa.
23 - Leite, J. P. G., A. A. Alfieri, P. A. Woods, R. I. Glass, and J. R. Gentsch. 1996. Rotavirus G and P types circulating in Brazil: characterization by RT-PCR, probe hybridization, and sequence analysis. Arch. Virol. 141:2365-2374.[CrossRef][Medline]
24 - Linhares, A. C., Y. B. Gabbay, J. D. P. Mascarenhas, R. B. de Freitas, C. S. Oliveira, N. Bellesi, T. A. F. Monteiro, Z. Lins-Laison, F. L. P. Ramos, and A. S. Valente. 1996. Immunogenicity, safety and efficacy of tetravalent rhesus-human, reassortant rotavirus vaccine in Belém, Brazil. Bull. W. H. O. 74:491-500.[Medline]
25 - Linhares, A. C., J. D. P. Mascarenhas, R. H. Gusmão, Y. B. Gabbay, A. M. Fialho, and J. P. G. Leite. 2002. Neonatal rotavirus infection in Belém, Northern Brazil: nosocomial transmission of P[6]G2 strain. J. Med. Virol. 67:418-426.[CrossRef][Medline]
26 - Maneekarn, N., and H. Ushijima. 2000. Epidemiology of rotavirus infection in Thailand. Pediatr. Int. 42:415-421.[CrossRef][Medline]
27 - Mascarenhas, J. D. P., R. H. P. Gusmão, C. R. M. Barardi, F. L. Paiva, C. O. Simões, Y. B. Gabbay, T. A. F. Monteiro, and A. C. Linhares. 1999. Characterization of rotavirus P genotypes circulating among paediatric inpatients in Northern Brazil. Rev. Inst. Med. Trop. Sao Paulo 41:165-170.[Medline]
28 - Mascarenhas, J. D. P., A. C. Linhares, Y. B. Gabbay, and J. P. G. Leite. 2002. Detection and characterization of rotavirus G and P types from children participating in a rotavirus vaccine trial in Belém, Brazil. Mem. Inst. Oswaldo Cruz 97:113-117.
29 - O'Halloran, F., M. Lynch, B. Cryan, H. O'Shea, and S. Fanning. 2000. Molecular characterization of rotavirus in Ireland: detection of novel strains circulating in the population. J. Clin. Microbiol. 38:3370-3374.[Abstract/Free Full Text]
30 - O'Mahony, J., B. Foley, S. Morgan, J. G. Morgan, and C. Hill. 1999. VP4 and VP7 genotyping of rotavirus samples recovered from infected children in Ireland over a 3-year period. J. Clin. Microbiol. 37:1699-1703.[Abstract/Free Full Text]
31 - Palombo, E. A., P. J. Masendycz, H. C. Bugg, N. Bogdanovic-Sakran, G. L. Barnes, and R. Bishop. 2000. Emergence of serotype G9 human rotavirus in Australia. J. Clin. Microbiol. 38:1305-1306.[Free Full Text]
32 - Parashar, U. D., J. S. Bresee, J. R. Gentsch, and R. I. Glass. 1998. Rotavirus. Emerg. Infect. Dis. 4:561-570.
33 - Ramachandran, M., B. K. Das, A. Vij, R. Kuma, S. S. Bhambal, N. Kesari, H. Rawat, L. Bahl, S. Thakur, P. A. Woods, R. I. Glass, M. K. Bhan, and J. R. Gentsch. 1996. Unusual diversity of human rotavirus G and P genotypes in India. J. Clin. Microbiol. 34:436-439.[Abstract]
34 - Ramachandran, M., J. R. Gentsch, U. D. Parashar, S. Jin, P. A. Woods, J. L. Holmes, C. D. Kirkwood, R. F. Bishop, H. B. Greenberg, S. Urasawa, G. Gerna, B. S. Coulson, K. Taniguchi, J. S. Bresee, R. I. Glass, and The National Rotavirus Strain Surveillance System Collaborating Laboratories. 1998. Detection and characterization of novel rotavirus strains in the United States. J. Clin. Microbiol. 36:3223-3229.[Abstract/Free Full Text]
35 - Rosa e Silva, M. L., I. P. de Carvalho, and V. Gouvea. 2002. 1998-1999 rotavirus seasons in Juiz de Fora, Minas Gerais, Brazil: detection of an unusual G3P[4] epidemic strain. J. Clin. Microbiol. 40:2837-2842.[Abstract/Free Full Text]
36 - Santos, N., R. C. C. Lima, C. F. A. Pereira, and V. Gouvea. 1998. Detection of rotavirus types G8 and G10 among Brazilian children with diarrhea. J. Clin. Microbiol. 36:2727-2729.[Abstract/Free Full Text]
37 - Santos, N., R. C. C. Lima, C. M. Nozawa, R. E. Linhares, and V. Gouvea. 1999. Detection of porcine rotavirus type G9 and a mixture of types G1 and G5 associated with Wa-like VP4 specificity: evidence for natural human-porcine genetic reassortment. J. Clin. Microbiol. 37:2734-2736.[Abstract/Free Full Text]
38 - Santos, N., E. M. Volotão, C. C. Soares, M. C. M. Albuquerque, F. M. da Silva, T. R. B. de Carvalho, C. F. A. Pereira, V. Chizhikov, and Y. Hoshino. 2001. Rotavirus strains bearing genotype G9 or P[9] recovered from Brazilian children with diarrhea from 1997 to 1999. J. Clin. Microbiol. 39:1157-1160.[Abstract/Free Full Text]
39 - Taniguchi, K., F. Wakasugi, Y. Ponsuwanna, T. Urasawa, S. Ukae, S. Chiba, and S. Urasawa. 1992. Identification of human and bovine rotavirus serotypes by polymerase chain reaction. Epidemiol. Infect. 109:303-312.[Medline]
40 - Timenetsky, M. C. T., N. Santos, and V. Gouvea. 1994. Survey of rotavirus G and P types associated with human gastroenteritis in São Paulo, Brazil, from 1986 to 1992. J. Clin. Microbiol. 32:2622-2624.[Abstract/Free Full Text]
41 - Unicomb, L. E., G. Podder, J. R. Gentsch, P. A. Woods, K. Z. Hasan, A. S. G. Faruque, M. J. Albert, and R. I. Glass. 1999. Evidence of high-frequency genomic reassortment of group A rotavirus strains in Bangladesh: emergence of type G9 in 1995. J. Clin. Microbiol. 37:1885-1891.[Abstract/Free Full Text]
42 - Zhou, Y., L. Li, B. Kim, K. Kaneshi, S. Nishimura, T. Kuroiwa, T. Nishimura, K. Sugita, Y. Ueda, S. Nakaya, and H. Ushijima. 2000. Rotavirus infection in children in Japan. Pediatr. Int. 42:428-439.[CrossRef][Medline]
Journal of Clinical Microbiology, July 2003, p. 3399-3402, Vol. 41, No. 7
0095-1137/03/$08.00+0 DOI: 10.1128/JCM.41.7.3399-3402.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Bourdett-Stanziola, L., Jimenez, C., Ortega-Barria, E.
(2008). Diversity of Human Rotavirus G and P Genotypes in Panama, Costa Rica, and the Dominican Republic. Am J Trop Med Hyg
79: 921-924
[Abstract]
[Full Text]
-
Phan, T. G., Khamrin, P., Quang, T. D., Dey, S. K., Takanashi, S., Okitsu, S., Maneekarn, N., Ushijima, H.
(2007). Detection and Genetic Characterization of Group A Rotavirus Strains Circulating among Children with Acute Gastroenteritis in Japan. J. Virol.
81: 4645-4653
[Abstract]
[Full Text]
-
Santos, N., Volotao, E. M., Soares, C. C., Campos, G. S., Sardi, S. I., Hoshino, Y.
(2005). Predominance of Rotavirus Genotype G9 during the 1999, 2000, and 2002 Seasons among Hospitalized Children in the City of Salvador, Bahia, Brazil: Implications for Future Vaccine Strategies. J. Clin. Microbiol.
43: 4064-4069
[Abstract]
[Full Text]
-
Sanchez-Fauquier, A., Wilhelmi, I., Colomina, J., Cubero, E., Roman, E.
(2004). Diversity of Group A Human Rotavirus Types Circulating over a 4-Year Period in Madrid, Spain. J. Clin. Microbiol.
42: 1609-1613
[Abstract]
[Full Text]