Table 3. Polymerase chain reaction (PCR) amplification of Simian immunodeficiency virus (SIV) sequences.
| Genus | Species | INNO-LIA posa PCR pos/tested | INNO-LIA ind PCR pos/tested | INNO-LIA neg PCR pos/tested |
|---|---|---|---|---|
| Cercocebus | agilis | 0/6 | 0/8 | 0/13 |
| torquatus | – | – | 0/1 | |
| Lophocebus | albigena | 0/2 | 0/2 | 0/7 |
| Cercopithecus | cephus | 2/25 | 0/7 | 0/56 |
| mona | ½ | – | 0/2 | |
| neglectus | 8/9 | – | 0/4 | |
| nictitans | 3/21 | 1/1 | 0/61 | |
| pogonias | 0/9 | 0/3 | 0/34 | |
| Chlorocebus | tantalus | 0/1 | – | 0/2 |
| Miopithecus | ogouensis | 2/3 | – | 0/10 |
| Erythrocebus | patas | – | – | 0/7 |
| Colobus | guereza | 6/6 | 0/1 | 1/16 |
| Mandrillus | sphinx | 4/5 | 0/1 | 0/4 |
| Papio | anubis | 0/2 | – | 0/11 |
| Total | 26/91 | 1/23 | 1/228 | |
aDNA was extracted from a subset of seropositive (pos), indeterminant (ind) and negative (neg) blood samples and subjected to nested PCR amplification by using HIV/SIV consensus pol primer pairs. In each column, the number of PCR-positive samples per total number of samples tested is indicated. The authenticity of all amplification products was confirmed by sequence analysis.