Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-24T14:59:20.183Z Has data issue: false hasContentIssue false

31 - Molecular evolution of papillomaviruses

Published online by Cambridge University Press:  04 May 2010

Adrian J. Gibbs
Affiliation:
Australian National University, Canberra
Charles H. Calisher
Affiliation:
Colorado State University
Fernando García-Arenal
Affiliation:
Universidad Politécnica de Madrid
Get access

Summary

Introduction

Papillomaviruses (PVs) are members of the genus Papillomavirus which, along with viruses of the genus Polyomavirus, comprise the family Papovaviridae (papillomavirus, polyomavirus and vacuolating agent). PVs are small, non-enveloped structures with icosahedral symmetry and a circular double-stranded DNA genome. They infect humans in addition to multiple other animal vertebrate species, resulting in a variety of proliferative epithelial lesions and tumours. Most papillomaviruses are species specific and have a cellular tropism for squamous epithelial cells. In benign papillomatous lesions, the viral genomes replicate as extrachromosomal episomes in the nuclei of basal and suprabasal epithelial cells. Complete vegetative replication with production of intact virions is found in the superficial and differentiated epithelial cells. In contrast, malignant lesions do not support vegetative viral replication, but instead often contain an integrated disrupted viral genome.

Sixty years ago, Richard Shope (1933) linked the presence of the cottontail rabbit papillomavirus (CRPV) to cutaneous papillomatosis in rabbits, and Francis Peyton Rous described the conversion of papilloma to squamous cell carcinoma in rabbits, initiating the field of tumour virology (Rous & Beard, 1935). Much of the current interest in papillomavirus research can be attributed to the recent association of human papillomaviruses (HPVs) with cervical cancer, one of the leading causes of cancer-attributed death in women.

Most of our knowledge of PVs has been obtained during the last decade through the use of recombinant DNA techniques. The small double-stranded DNA genomes of PVs have been readily amenable to cloning and sequencing. In the absence of a serological classification, HPVs have been categorized according to their genotype.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×