Abstract

Genetic diversity, attributable to the low fidelity of reverse transcription, recombination and mutation, is an important feature of infectious retroviruses. Under selective pressure, such as that imposed by superinfection interference, gammaretroviruses commonly adapt their envelope proteins to use alternative receptors to overcome this entry block. The first characterized koala retroviruses KoRV subgroup A (KoRV-A) were remarkable in their absence of envelope genetic variability. Once it was determined that KoRV-A was present in all koalas in US zoos, regardless of their disease status, we sought to isolate a KoRV variant whose presence correlated with neoplastic malignancies. More than a decade after the identification of KoRV-A, we isolated a second subgroup of KoRV, KoRV-B from koalas with lymphomas. The envelope proteins of KoRV-A and KoRV-B are sufficiently divergent to confer the ability to bind and employ distinct receptors for infection. We have now obtained a number of additional KoRV envelope variants. In the present studies we report these variants, and show that they differ from KoRV-A and KoRV-B envelopes in their host range and superinfection interference properties. Thus, there appears to be considerable variation among KoRVs envelope genes suggesting genetic diversity is a factor following the KoRV-A infection process.

Highlights

  • A retrovirus has been implicated in the lymphoid neoplasias that have been plaguing koalas for the last several decades [1,2]

  • peripheral blood mononuclear cells (PBMCs) collected from all tested koalas in U.S zoos produce KoRV subgroup A (KoRV-A). [14]

  • PBMCs obtained from a koala infected with KoRV-A and KoRV-B

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Summary

Introduction

A retrovirus has been implicated in the lymphoid neoplasias that have been plaguing koalas for the last several decades [1,2]. In 2000, a group of Australian scientists isolated, characterized, and sequenced a gammaretroviral provirus present in feral and captive koalas [3]. KoRV-A has several distinctive features, one being that it is an endogenous retrovirus [4]. KoRV-A is an endogenous retrovirus, it is not present in all koala genomes. It appears to be spreading through the koala population from koalas in the north to those living in the south [6,7]

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