Volume 17, Number 5—May 2011
Dispatch
Detection and Phylogenetic Characterization of Human Hepatitis E Virus Strains, Czech Republic
Table A1
Patient no. | Age, y/sex | Town of origin | Possible risk factors | Bilirubin, μmol/L | ALT, μkat/L | AST, μkat/L | GGT μkat/L | ALP, μkat/L | Systemic disease | Hospital care, d | Isolate name | ORF1† | ORF2/3 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1‡ | 62/M | A | NS | 152.00 | 38.40 | 19.30 | 5.60 | 4.83 | NS | 13 | CZhHEV107-09 | ||
2‡ | 66/M | B | Ate homemade slaughter products; used same knife and chopping board for raw and cooked meat; ate undercooked meat in sushi bar | 110.00 | 40.78 | 8.72 | 15.37 | 4.73 | NS | 11 | CZhHEV108-09 | + | + |
3‡ | 62/M | B | Used same knife and chopping board for raw and cooked meat | 614.00 | 25.22 | 28.78 | 4.98 | 5.77 | DM, IHD | 41 | CZhHEV113-09 | + | + |
4‡ | 75/M | B | NS | 203.00 | 20.24 | 28.57 | 2.68 | 3.35 | NS | 15 | CZhHEV117-09 | + | + |
5‡ | 77/F | B | Ate pork | 77.00 | 78.87 | 51.78 | 8.92 | 6.92 | NS | 10 | CZhHEV114-09 | – | + |
6‡ | 59/M | B | NS | 297.00 | 88.44 | 45.57 | 4.52 | 2.50 | CLL | 10 | ND | + | + |
7‡ | 59/M | C | Ate raw meat | 14.50 | 8.99 | 5.52 | 1.96 | 2.24 | NS | 8 | ND | – | – |
8§ | 65/F | C | NS | 36.30 | 2.32 | 0.90 | 8.76 | 4.83 | BC, CH | 11 | ND | – | – |
9§ | 27/F | C | Visited China | 5.80 | 1.89 | 2.08 | 1.03 | 1.40 | NS | 7 | ND | – | – |
10§ | 53/M | C | NS | 113.10 | 19.48 | 20.43 | 20.52 | 10.49 | SM | 14 | CZhHEV197-09 | – | – |
*HEV, hepatitis E virus; RT-PCR, reverse transcription–PCR; ALT, alanine aminotransferase; AST, aspartate aminotransferase; GGT, gama-glutamyltransferase; ALP, alkaline phosphatase; ORF1, primers targeting open reading frame 1 of HEV genome; ORF2/3, primers targeting overlapping part of HEV ORF2 and ORF3; NS, not shown; DM, diabetes mellitus; IHD, ischemic heart disease; CLL, chronic lymphatic leukemia; ND, not detected; BC, breast cancer; CH, chronic hepatopathy; SM, smoldering myeloma.
†Specific PCR product sequenced.
‡Detection of immunoglobulin (Ig) G antibodies against HEV by EIAgen HEV IgM kit (Adaltis, Rome, Italy), EIAgen HEV IgG Kit (Adaltis) and Recomblot HEV IgM/IgG (Microgen GmbH, Neured, Germany).
§Detection of IgM antibodies against HEV by HEV IgM ELISA 3.0 (MP Diagnostics, Illkirch Cedex, France) and HEV ELISA (MP Diagnostics).