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J Gen Virol 85 (2004), 3189-3194; DOI 10.1099/vir.0.80248-0

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© 2004 Society for General Microbiology

Evidence for hepatitis E virus quasispecies

Marc Grandadam1, Soraya Tebbal2, Mélanie Caron1, Mahinda Siriwardana3, Bernard Larouze3, Jean Louis Koeck1, Yves Buisson1, Vincent Enouf1 and Elisabeth Nicand1

1 Laboratoire de Biologie Clinique, HIA Val de Grâce, 74 boulevard de Port Royal, 75230 Paris cédex 05, France
2 Service de Maladies Infectieuses, CHU de Batna, Batna, Algeria
3 Unité de Recherche "Epidémiologie et Sciences de l'Information", INSERM U444, Faculté de Médecine de Saint Antoine, 27, rue de Chaligny, 75571 Paris cédex 12, France

Correspondence
Elisabeth Nicand
rt{at}filnet.fr

The genetic diversity of hepatitis E virus (HEV) has been extensively analysed during the last decade. Most sporadic and epidemic HEV strains are distributed into genotypes or groups. Nevertheless, few studies have looked at the polymorphism of HEV strains isolated from a given outbreak. A serum bank collected in Tanefdour, Algeria, during an acute hepatitis epidemic (1986–1987), retrospectively confirmed as hepatitis E, was analysed. Of the 69 serum samples collected within an 8-week period, 23 were positive for both partial ORF1 (replicase gene) and ORF2 (capsid gene) sequences. Inter- and intra-patient diversities were assessed by RFLP, and by sequencing a 448 bp sequence corresponding to ORF2. RFLP analysis distinguished three profiles: A (18/23), B (3/23) and C (2/23). Most isolates (18/23) shared 99·7–100 % sequence identity and the remainder showed 1–1·3 % divergence. HEV intra-patient diversity was studied using 12 isolates (seven displaying the major RFLP profile and five displaying minor RFLP profiles). For 9 of 12 isolates, additional intra-patient heterogeneity was revealed by RFLP analysis of 100 clones from each isolate and sequence diversity ranging from 0·11 to 3·4 %. These data strongly support the quasispecies organization of HEV during epidemics and could explain the adaptable behaviour of the virus in the host–pathogen interrelations.

The GenBank/EMBL/DDBJ accession numbers for the nucleotide sequences reported in this paper are AY568357AY568365, AY596462 and AY596463.




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