Virus Dataset Sample Info

> Dataset: 33687074 Search Result


Summary
Item Summary
Project 33687074
Virus Name HBV
Sample Number 32
Disease HBV infection
Country Brazil
Data Link https://www.ncbi.nlm.nih.gov/nuccore/?term=MN758680:MN758724[pacc]

Sample
ID Sample ID Age Gender Origin Detail
1 952-17 39 M Brazil View
2 502-17 55 M Brazil View
3 131-18 42 M Brazil View
4 363-18 42 F Brazil View
5 651-18 57 M Brazil View
6 814-18 53 M Brazil View
7 998 26 M Brazil View
8 767 59 M Brazil View
9 642 38 F Brazil View
10 676 31 M Brazil View
11 364 38 M Brazil View
12 520 63 M Brazil View
13 3 57 M Brazil View
14 121 59 M Brazil View
15 174 46 M Brazil View
16 214 57 F Brazil View
17 286 43 F Brazil View
18 317 35 M Brazil View
19 332 47 M Brazil View
20 381 51 M Brazil View
21 392 55 M Brazil View
22 665 31 M Brazil View
23 692 31 M Brazil View
24 753 30 M Brazil View
25 926 50 F Brazil View
26 1009 41 M Brazil View
27 1054 57 F Brazil View
28 1493 47 M Brazil View
29 1546 34 M Brazil View
30 1587 47 M Brazil View
31 1633 32 M Brazil View
32 1781 51 M Brazil View

Literature
Item Summary
PMID 33687074
Title Occult and active hepatitis B virus detection in donated blood in Sao Paulo, Brazil.
Abstract BACKGROUND: The present study determined the HBV antigen, antibody, and DNA status in blood donations deemed to be HBV positive. Individuals with an occult HBV infection (OBI), defined as being positive for HBV DNA but negative for HBV surface antigen (HBsAg), as well as those with active infection (HBsAg-positive), were identified and characterized. STUDY DESIGN AND METHODS: From a total pool if 198,363 blood donations, we evaluated in a cross-sectional study, 1106 samples that were positive in screening tests for antibody to HBV core antigen (HBcAb), HBsAg, and/or HBV DNA by nucleic acid testing (NAT-HBV). The presence of genetic variants in the HBV pol/S gene in individuals with an active HBV infection was also determined. RESULTS: OBIs were detected in six of 976 samples (0.6%) that were positive only for HBcAb. The rate of HBV active infection was 0.024% (48/198,363) and there was a predominance of HBV sub-genotype A1 (62.2%, 28/45), followed by D3 (17.8%, 8/45). Mutations in the S gene were found in 57.8% (26/45) and immune escape mutations in 37.8% (17/45) of active HBV-infected donors. Among them, T123N, G145A, and D144G high-impact immune escape mutations were identified. CONCLUSION: Highly sensitive molecular tests improve the capacity to detect OBIs. When NAT is performed in pooled samples, HBcAb test has value in the detection of donors with OBI and improves transfusion safety. Mutations in the S gene are frequent in HBsAg-positive blood, including those associated with diagnostic failure and vaccine escape mutations.