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. 2017 May 22;5:108. doi: 10.3389/fpubh.2017.00108

Table 3.

Results of the screening for XMRV performed on human and animal sampling populations.

Sampling population DNA source N No. of positive samples No. of negative samples Primers Comments
Human ME/CFS patients Peripheral blood 47 2 45 1 + 2 Amplicons were not reproducible and often associated with spurious extra-bands
Human controls Peripheral blood 53 0 53 1 + 2
Laboratory mouse strain BDF Peripheral blood 1 1 0 1 + 2 Reproducible band of the correct size. Identity was confirmed by sequencing
Laboratory mouse strain Ts65Dn Tail tip 10 10 0 1 + 2 Scarce reproducibility of independent amplifications. Extra-bands were often observed
Laboratory white rat (Wistar) Tail tip 10 0 10 2
Brown laboratory rat (Rattus norvegicus) Tail tip 5 0 5 2
Wood mouse (Apodemus sylvaticus) Tail tip 11 ? ? 2 Very scarce reproducibility: two samples were positive in 4/7 repetitions; five in 2/7 repetitions
Non-reproducible extra-bands were always observed
Badger (Meles meles) Fur 25 0 25 2
Stone marten (Martes foina) Feces 15 0 15 1 + 2
Weasel (Mustela nivalis) Feces 15 0 15 2
Fox (Vulpes vulpes) Peripheral blood 14 0 14 1 + 2
Hare (Lepus europaeus) Peripheral blood 23 0 23 2
Bovines (various breeds) Peripheral blood 23 0 23 1 + 2

All amplifications have been repeated at least twice, always in the presence of the positive control (BDF laboratory mouse). Sequencing has been performed on amplicons obtained with our new primers. 1: primers by Ref. (31); 2: newly designed primers.

?: variable among repetitions.