Abstract

BackgroundHTLV-1 infection is endemic among people of Melanesian descent in Papua New Guinea, the Solomon Islands and Vanuatu. Molecular studies reveal that these Melanesian strains belong to the highly divergent HTLV-1c subtype. In Australia, HTLV-1 is also endemic among the Indigenous people of central Australia; however, the molecular epidemiology of HTLV-1 infection in this population remains poorly documented.FindingsStudying a series of 23 HTLV-1 strains from Indigenous residents of central Australia, we analyzed coding (gag, pol, env, tax) and non-coding (LTR) genomic proviral regions. Four complete HTLV-1 proviral sequences were also characterized. Phylogenetic analyses implemented with both Neighbor-Joining and Maximum Likelihood methods revealed that all proviral strains belong to the HTLV-1c subtype with a high genetic diversity, which varied with the geographic origin of the infected individuals. Two distinct Australians clades were found, the first including strains derived from most patients whose origins are in the North, and the second comprising a majority of those from the South of central Australia. Time divergence estimation suggests that the speciation of these two Australian clades probably occurred 9,120 years ago (38,000–4,500).ConclusionsThe HTLV-1c subtype is endemic to central Australia where the Indigenous population is infected with diverse subtype c variants. At least two Australian clades exist, which cluster according to the geographic origin of the human hosts. These molecular variants are probably of very ancient origin. Further studies could provide new insights into the evolution and modes of dissemination of these retrovirus variants and the associated ancient migration events through which early human settlement of Australia and Melanesia was achieved.

Highlights

  • The Human T-lymphotropic virus type 1 (HTLV-1) is the first described human oncoretrovirus [1]

  • The HTLV-1c subtype is endemic to central Australia where the Indigenous population is infected with diverse subtype c variants

  • We compared the gp21 env gene fragments of seven proviral sequences from Australia, including five new proviral strains (Aus-Cs, Australian proviral sequences (Aus)-DF, Aus-NR, Aus-GN and Aus-GM) and two previously characterized sequences (MSHR-1 and Aus-RDJ) (Genbank: M92818 and JX891480, respectively) [15,25], with HTLV-1 proviral strains from Papua New Guinea (PNG) (MEL1, MEL2 and MEL7), Vanuatu (EM5, VAN54, VAN136, VAN251 and PE376) and the Solomon Islands (MEL3 to MEL6 and MEL8 to MEL10) [9,13,18,31]

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Summary

Introduction

The Human T-lymphotropic virus type 1 (HTLV-1) is the first described human oncoretrovirus [1]. HTLV-1 infects at least 5 to 10 million people worldwide [3] It is widely distributed, with substantial clusters of high endemicity in certain geographic areas and ethnic groups in Southwestern Japan, sub-Saharan Africa, South America, the Caribbean basin and smaller endemic foci in Iran and Australo-Melanesia [3]. Seven main molecular HTLV-1 subtypes are currently recognized, predominantly from nucleotide sequence analysis of the LTR region. These are the Cosmopolitan subtype (a) that has spread worldwide, five African subtypes (b, dg) and an Australo/Melanesian subtype (c), which is found only in Oceania [4,5,6,7,8]. In Australia, HTLV-1 is endemic among the Indigenous people of central Australia; the molecular epidemiology of HTLV-1 infection in this population remains poorly documented

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