Selection Pressure-Driven Evolution of the Epstein-Barr Virus-Encoded Oncogene LMP1 in Virus Isolates from Southeast Asia

Author:

Burrows Jacqueline M.1,Bromham Lindell2,Woolfit Megan2,Piganeau Gwenaël2,Tellam Judy1,Connolly Geoff1,Webb Natasha1,Poulsen Leith1,Cooper Leanne1,Burrows Scott R.1,Moss Denis J.1,Haryana Sofia M.3,Ng Mun4,Nicholls John M.4,Khanna Rajiv1

Affiliation:

1. Tumour Immunology Laboratory, Division of Infectious Diseases and Immunology, Queensland Institute of Medical Research, The Bancroft Centre, and Joint Oncology Program, Department of Molecular and Cellular Pathology, University of Queensland, Brisbane, Australia

2. Centre for the Study of Evolution, School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom

3. Department of Pathology, University of Hong Kong, Hong Kong SAR, People's Republic of China

4. Faculty of Medicine, Gadjah Mada University, Yogyakarta, Indonesia

Abstract

ABSTRACT The geographically constrained distribution of Epstein-Barr virus (EBV)-associated nasopharyngeal carcinoma (NPC) in southeast Asian populations suggests that both viral and host genetics may influence disease risk. Although susceptibility loci have been mapped within the human genome, the role of viral genetics in the focal distribution of NPC remains an enigma. Here we report a molecular phylogenetic analysis of an NPC-associated viral oncogene, LMP1 , in a large panel of EBV isolates from southeast Asia and from Papua New Guinea, Africa, and Australia, regions of the world where NPC is and is not endemic, respectively. This analysis revealed that LMP1 sequences show a distinct geographic structure, indicating that the southeast Asian isolates have evolved as a lineage distinct from those of Papua New Guinea, African, and Australian isolates. Furthermore, a likelihood ratio test revealed that the C termini of the LMP1 sequences of the southeast Asian lineage are under significant positive selection pressure, particularly at some sites within the C-terminal activator regions. We also present evidence that although the N terminus and transmembrane region of LMP1 have undergone recombination, the C-terminal region of the gene has evolved without any history of recombination. Based on these observations, we speculate that selection pressure may be driving the LMP1 sequences in virus isolates from southeast Asia towards a more malignant phenotype, thereby influencing the endemic distribution of NPC in this region.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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