Simian T-Lymphotropic Virus Diversity among Nonhuman Primates, Cameroon
David M. Sintasath, Nathan D. Wolfe
1, Matthew LeBreton, Hongwei Jia, Albert D. Garcia, Joseph Le Doux Diffo, Ubald Tamoufe, Jean K. Carr, Thomas M. Folks, Eitel Mpoudi-Ngole, Donald S. Burke
2, Walid Heneine, and William M. Switzer
Author affiliations: Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA (D.M. Sintasath, D.S. Burke); University of California School of Public Health, Los Angeles, California, USA (N.D. Wolfe, U. Tamoufe); Johns Hopkins Cameroon Program, Yaoundé, Cameroon (M. LeBreton, J.L.D. Diffo, U. Tamoufe, E. Mpoudi-Ngole); Centers for Disease Control and Prevention, Atlanta, Georgia, USA (H. Jia, A. D. Garcia, T.M. Folks, W. Heneine, W.M. Switzer); University of Maryland Biotechnology Institute, Baltimore (J.K. Carr)
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Figure 4
Figure 4. Identification of a novel primate T-lymphotropic virus (PTLV) subtype by phylogenetic inference of 881-bp tax sequences from prototypical PTLVs. Bovine leukemia virus (BLV) tax sequences were used as an outgroup in the maximum-likelihood analysis. New sequences from this study are in boldface. Support for the branching order was determined by 1,000 bootstrap replicates; only values >60% are shown. Branch lengths are proportional to the evolutionary distance (scale bar) between the taxa. See Figure 2 legend for abbreviations.
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