Volume 22, Number 4—April 2016
Research
Evaluation of Viremia Frequencies of a Novel Human Pegivirus by Using Bioinformatic Screening and PCR
Table 3
Virus, ID no. | Case-patient origin | Type† | Length | Coverage, % | Reads | Div, %‡ | dN/dS | MFED, %§ |
---|---|---|---|---|---|---|---|---|
HHpgV-1, n = 2 | ||||||||
D1220 | UK | NA | 9,550 | 99.8 | 247,798 | 4.7 | 0.193 | 7.6 |
D1255 |
UK |
NA |
9,503 |
99.6 |
101,951 |
5.1 |
0.170 |
8.3 |
HPgV, n = 20 | ||||||||
89859249 | UK | 2 | 9,383 | 99.9 | 19,231,581 | 10.0 | 0.031 | 11.4 |
89859262 | UK | 2 | 9,388 | 99.8 | 6,766,497 | 9.9 | 0.029 | 12.4 |
56330218 | South Africa | 5 | 9,364 | 99.7 | 4,242,732 | 13.6 | 0.043 | 11.6 |
56330227 | Australia | 2 | 9,366 | 99.7 | 2,411,508 | 9.9 | 0.031 | 12.0 |
56330281 | DRC | 1 | 9,362 | 99.7 | 2,297,064 | 13.5 | 0.048 | 13.2 |
67845223 | UK | 2 | 9,382 | 99.9 | 1,332,130 | 9.4 | 0.023 | 11.5 |
56330260 | UK | 5 | 9,365 | 99.7 | 1,306,864 | 13.7 | 0.043 | 12.1 |
56330265 | UK | 2 | 9,425 | 99.7 | 1,178,508 | 9.5 | 0.035 | 12.5 |
56330292 | NA | 2 | 9,356 | 99.6 | 1,021,219 | 11.5 | 0.035 | 11.9 |
89860237 | UK | 2 | 9,367 | 99.7 | 953,683 | 9.5 | 0.035 | 11.0 |
56330272 | DRC | 1 | 9,340 | 99.4 | 707,495 | 13.6 | 0.052 | 12.0 |
56330229 | UK | 2 | 9,366 | 99.7 | 698,622 | 11.5 | 0.036 | 12.6 |
56330276 | DRC | 5 | 9,337 | 99.4 | 612,424 | 13.3 | 0.042 | 12.3 |
89860282 | UK | Novel | 8,443 | 89.9 | 574,652 | 13.2 | 0.049 | 10.5 |
89860286 | UK | 2 | 8,923 | 95.0 | 513,420 | 9.6 | 0.035 | 10.3 |
89860260 | UK | 2 | 8,983 | 95.6 | 512,515 | 11.6 | 0.041 | 10.5 |
56330286 | NA | 2 | 9,355 | 99.6 | 454,106 | 9.6 | 0.022 | 12.5 |
56330228 | Australia | ND | 436 | 4.6 | 68,351 | 8.6 | 0.019 | ND |
56330250 | UK | ND | 423 | 4.5 | 38,083 | 11.6 | 0.043 | ND |
89860212 |
UK |
ND |
1,117 |
11.9 |
17,226 |
8.6 |
0.068 |
ND |
*HPgV, human pegivirus; ID, identification; Div, sequence divergence; dN/dS: ratio of nonsynonymous (dN) to synonymous (dS) substitutions; MFED, mean folding energy difference; HHpgV, human hepegivirus; UK, United Kingdom; NA, not applicable (no genotypes of HHpgV-1 are currently assigned); DRC, Democratic Republic of Congo; ND, not done (insufficient sequence length). †Genotype based on phylogenetic analysis of complete genome sequences (Figure 1). ‡Comparison with AK790 prototype sequence (HHPgV-1) or AF121950 (HPgV; genotype 2). §Difference in minimum folding energy of sequences compared with those of sequence order-randomized controls (MFED) (16). |
Page created: March 15, 2016
Page updated: March 15, 2016
Page reviewed: March 15, 2016
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.