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Journal of Clinical Microbiology, June 1999, p. 1699-1703, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
VP4 and VP7 Genotyping of Rotavirus Samples Recovered from
Infected Children in Ireland over a 3-Year Period
Jim
O'Mahony,1,2
Barbara
Foley,1,2
Sheila
Morgan,1,2
John G.
Morgan,1 and
Colin
Hill1,2,*
Department of
Microbiology1 and National Food
Biotechnology Centre,2 University College,
Cork, Ireland
Received 21 December 1998/Returned for modification 4 February
1999/Accepted 23 February 1999
Between September 1995 and August 1998, the incidence and diversity
of the main human rotavirus genotypes (G1, G2, G3, and G4 and
P[8], P[4], P[6], and P[9]) among Irish children were
determined by using established and adapted reverse transcriptase
PCR-based genotyping methods. From a total of 193 rotavirus-positive
specimens collected from nine hospitals we successfully identified the
P type in 182 (94%) of the samples and the G type in 165 (85.5%) of
the samples. Only four samples could not be assigned a G or P type. Two
P types existed in Ireland, P[8] (78%) and P[4] (16%), and their
relative incidence varied over the 3 years of this study. No P[6] or
P[9] types were detected. G1 was the most predominant G type (55%),
and the incidences of G2, G3, and G4 isolates were 15.5, 1, and 11%, respectively. Three percent of the samples tested had a
mixed G type. A P and G type was assigned to 158 (81.8%) of samples.
Of the typeable samples, G1 P[8] was the most prevalent (65%),
whereas G2 P[4] (17%), G3 P[8] (1%), G4 P[8] (12%), and mixed
types (all G1/ G4 P[8]) (4%) were detected less frequently. In the
third year a significant genotypic shift from G1 P[8] to G2 P[4]
and G4 P[8] was observed. During the study, we noticed that the
inclusion of random primers during cDNA synthesis greatly increased the
specificity of the PCR typing assays. No correlation was seen between
the contributing hospitals and a specific genotype. In conclusion, the
coverage of infection given by the recently licensed
tetravalent vaccine would be significantly high in Ireland, although
future monitoring of genotypic changes among Irish isolates should be encouraged.
*
Corresponding author. Mailing address:
Microbiology Department, University College Cork, College Rd., Cork,
Ireland. Phone: 353-21-902397. Fax: 353-21-903101. E-mail:
c.hill{at}ucc.ie.
Journal of Clinical Microbiology, June 1999, p. 1699-1703, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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