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 6
Figure 6. Inferred phylogenetic relationships of primate T-lymphotropic virus (PTLV)–1 long terminal repeat (LTR) sequences by neighbor-joining analysis. Sequences from wild nonhuman primates (NHPs) in Cameroon generated in the current study are in boldface. Human T-lymphotropic virus–1 seqences are italicized. Support for the branching order was determined by 1,000 bootstrap replicates; only values >60% are shown. STLV, simian T-lymphotropic virus. See Figure 2 legend for additional abbreviations.
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