Our result confirms previous reports that pyrosequencing is the most YAP-TEAD Inhibitor 1 concentration sensitive method available for detecting small subpopulations of resistant virus and, as such, is likely to become the method of choice in the near future [7, 19, 20, 27, 28]. Figure 1 Pyrosequencing analysis with allelic quantification of A/G for the first position of codon M/ATG and V/GTG in different mixtures of WT (YMDD) and MUT (YVDD) plasmids. (A) 100% WT-0% MUT; (B) 50% WT-50% MUT; (C) 66% WT33% MUT; (D) 90% WT-10% MUT; (E) 95% WT-5% MUT. The results of quantification

of each nucleotide are indicated above the pyrograms (as %). Comparisons of YMDD variants in serum of patients with acute and chronic HBV infection detected

by direct sequencing and pyrosequencing are shown in Table 1. As expected, none of the individuals VX-689 ic50 with acute hepatitis B had LAM-resistant isolates as a dominant virus population, whether detected by direct sequencing or pyrosequencing. However, because of its greater ability to detect viral subpopulations, pyrosequencing revealed that 11/20 (55%) of the individuals with acute hepatitis B had only AZD0530 ic50 WT isolates, whereas 9/20 (45%) had minor subpopulations of LAM-resistant isolates varying from 4% to 17%. The detection of pre-existing resistant variants in acute phase provides information helpful in choosing an appropriate antiviral regimen whether individuals have become chronic carriers, and thus need to start an antiviral regimen. Thirty-eight patients (86.4%) with chronic hepatitis B were undergoing a LAM monotherapy regimen,

whereas the other six (13.6%) were receiving combination therapy of LAM plus adefovir dipivoxil (ADV) or tenofovir disoproxil fumarate (TDF). There was no significant association between the treatment duration and the occurrence of LAM-resistant isolates. Direct sequencing methods determined that WT isolates were present (-)-p-Bromotetramisole Oxalate in 19 of 44 patients (43.2%) and LAM-resistant isolates were present in 25 of 44 patients (56.8%), with a predominance of the YVDD variant (17/25, 68%) compared to the YIDD variant (8/25, 32%). Pyrosequencing confirmed the presence of exclusively WT isolates in 10 of 19 samples (52.6%) characterized as WT by direct sequencing. In the other nine samples (47.4%), pyrosequencing was able to detect the presence of minor subpopulations of LAM-resistant isolates. Of 25 samples characterized as LAM-resistant by direct sequencing, pyrosequencing confirmed the presence of only one population of resistant mutants (either YVDD or YIDD) in 14 (56%).