Shope papilloma virus

Engraving from Tableau Encyclopedique et Methodique, 1789.

The cottontail rabbit papilloma virus (CRPV), or Shope papilloma virus (also known as Kappapapillomavirus 2, Cottontail rabbit papillomavirus, and Rabbit (Shope) papilloma virus), is a type I virus under the Baltimore scheme, possessing a nonsegmented dsDNA genome. In the 1930s, hunters in northwestern Iowa reported that the rabbits they shot had several horn protrusions on many parts of their bodies including their faces and necks (Shope et. al 1933). This lead to the investigation and discovery of the virus in 1933 by Richard E. Shope when he was experimenting with cancer research (Klein et. al 1981). Shope separated the virus from horny warts on cottontail rabbits, and made one of the first mammaliam tumor virus discoveries (Klein et. al 1981).

The virus is also a possible source of myths about the jackalope, a rabbit with the horns of an antelope, and related cryptids such as the wolpertinger. Stories and illustrations of horned rabbits appear in scientific treatises dating back many years, such as the Tableau encyclopédique et méthodique, from 1789.

Richard Edwin Shope, discovered Shope papillomavirus

Shope determined the “horn” protrusions were keratinous carcinomas due to the infection of CRPV. These are typically found on or near the animal’s head, and can become large enough to interfere with the host’s ability to eat, causing starvation. The virus was originally discovered to affect only cottontail rabbits (Sylvilagus spp.) in the Midwestern U.S., but can also infect brush rabbits, jackrabbits (Lepus californicus), snowshoe hares (Lepus americanus), and house rabbits (Oryctolagus cuniculus) (Praag et. al 2003).

Shope’s research has led to the development of an SPV model and the first mammalian model of a cancer caused by a virus. He was able to isolate virus particles from tumors on captured animals and use these to inoculate domestic rabbits, which then developed similar tumors. The animal model of the Shope Papilloma Virus (SPV) has contributed to our understanding of fundamental mechanisms in neoplasia, or the formation of a new, abnormal growth of tissue (Klein et. al. 1981). The virus was sequenced in 1984, showing substantial sequence similarities to HPV1a. It has been used as a model for human papillomaviruses both before and after this discovery. The most visible example of this role is the HPV vaccine, which was developed based on and incorporating research done using the virus as a model. Similarly, it has been used to investigate antiviral therapies.

Genome

There is a lack of specific data about the productive cycle of papillomaviruses. Research is not conclusive about which coding regions are expressed before or after replication of viral DNA. The E1 region should carried the DNA required for cis and/or trans. E1 is the largest Open reading frame, which is the set of codons in the genome that code for proteins, encoding a 602 base protein. E1 is similar to COOH-terminal domain of the Simian virus 40, plays a role in viral DNA replication maintaining plasmids within a cell. Results have found that CRPV and BPV1 are found in the same location of the genome, which is indicates that papillomaviruses likely have similar methods of replicating their genomes outside of a chromosome. Notable difference between the genomes of the four strains is that the E6 protein is almost twice as long in the CRPV as in any of the other strains of papillomaviruses. The E6 protein is somewhat homologous with a family of ATP synthases that are found in mitochondria of cattle. The homology is significant enough to imply an evolutionary relationship between E6 and the beta chain of the ATP synthase family, however they do not have the same same function or enzyme activity. The E2 protein overlaps with the E4 open reading frames in the other papillomaviruses. These differences in the E2 proteins likely determine how oncogenic a virus is. The noncoding region has a homologies with BPV1. Other homologies exist, such as the fact that all papillomaviruses have repeated sequences in the noncoding parts of their genomes. CRPV has some notable repeats, some as long as 32 base pairs. Many pairs up stream of the transcription locations are homologous with promoter sequences in of SV40 (Giri et. al 1985).

Life cycle

Replication cycle and transcription

The Papillomavirus life cycle begins with cells actively multiplying in epithelial cells of basal and parabasal layers. The differentiation of these cells is necessary for this virus to complete its life cycle. Transforming proteins E6 and E7 induce the S-phase in the lower epithelial layers (Doorbar et. al 2004). Viral replication proteins E1 and E2 are also required to form the papilloma and keep the episomal viral genome replication low. Genome amplification will be restrained until viral replication proteins increase and several viral proteins are co-expressed. The infected, differentiating cells travel towards the epithelial surface during the viral cycle’s late stage. In the upper epithelial layers, the promoter activity is altered during the virus’ production. E4 proteins are expressed, and viral DNA amplification starts in the differentiated cells. Following this, the L1 and L2 viral capsid proteins are expressed and the infectious virions begin to assemble (Peh et. al 2004).

The Papillomavirus life cycle begins with cells actively multiplying in epithelial cells of basal and parabasal layers. The differentiation of these cells is necessary for this virus to complete its life cycle. Transforming proteins E6 and E7 induce the S-phase in the lower epithelial layers (Doorbar et. al 2004). Viral replication proteins E1 and E2 are also required to form the papilloma and keep the episomal viral genome replication low. Genome amplification will be restrained until viral replication proteins increase and several viral proteins are co-expressed. The infected, differentiating cells travel towards the epithelial surface during the viral cycle’s late stage. In the upper epithelial layers, the promoter activity is altered during the virus’ production. E4 proteins are expressed, and viral DNA amplification starts in the differentiated cells. Following this, the L1 and L2 viral capsid proteins are expressed and the infectious virions begin to assemble (Peh et. al 2004).

Expression of the papillomavirus E4 protein correlates with the onset of viral DNA amplification. Using a mutant cottontail rabbit papillomavirus (SPV) genome incapable of expressing the viral E4 protein, it has been shown that E4 is required for the productive stage of the SPV life cycle in New Zealand White and cottontail rabbits (Doorbar 2004).

Assembly and release

The virus particles are assembled in the upper epithelium. The virus capsomere icosahedral shell is packaged with an 8000 base pair genome, 360 L1 protein copies, and 12 copies of L2 proteins inside. L2 proteins gather at PML body nuclear structures and recruit L1 proteins during virus assemblage. L2 proteins are not necessary for assemblage, but it is possible that they augment packaging and infectivity. Capsid proteins have been thought to also gather at the PML bodies during packaging (Doorbar et. al 2004).

Transmittance of the Papillomavirus requires release from the infected skin cell at the epithelial surface, as they are non-lytic. They are resistant to desiccation, enhancing their survivability during extracellular transfer between hosts. Cornified squame release from the surface of epithelial cells may also contribute to their survival. Immune detection of the virus in the host may also be hindered by antigen retention until the virus reaches upper epithelial cells (Doorbar et. al 2004).

Modulation of host processes

When Richard E. Shope began his research on SPV, little was known about the natural transmission of the virus vectors and interactions of the virus on its hosts. In the lab setting, Shope worked with the virus’ natural host, the cottontail rabbit (Klein et.al). Particularly, he worked with the cottontails of Iowa and other western states of the United States. He worked with these species because it was discovered that SPV had a restricted geographic range and was confined to the high plains of the western United States (Klein et. al.). Therefore the major host species of SPV is the cottontail rabbit of the western United States. Cottontail rabbits in Shope’s lab usually were infected with the virus through parasites such as rabbit ticks (Klein). When infected with SPV, hosts develop papillomas on hair-bearing skin, usually around the face and neck (Klein). Shope found through his research that rabbit epidermal cell transformation by SPV requires interaction with mesenchymal cells. It was further found that mesenchymal types support papillomatous transformation (Klein). Shope’s research also investigated how vitamin A deficiencies or excess might affect host susceptibility to SPV. Shope found that deficiencies in vitamin A did not affect the relative growth of the papillomas, but in cases where there was excesses of vitamin A Shope papillomas were inhibited (Klein). Therefore when SPV infects a host, vitamin A plays an important role in the host/virus interactions.

Location in the host

Fluorescent antibody study identified the locations of viral antigens in wild rabbit papillomas. They were present only in the nucleus of keratohyaline and keratinized layer cells, and not deeper down in proliferating epithelial cells. In domesticated rabbits, the viral antigens were present in much smaller quantity in only superficial, keratinized layers. The investigation proposed that the virus is only present in proliferating cell nuclei during early development, containing a deficient amount of proteins and mostly nucleic acid. The proteins may be immunologically specific in order keep its transmissibility, making it a masked virus (Noyes et. al 1957).

Associated viruses

Most homologous papillomaviruses are actually CRPV and HPV1a. This is possibly because both of these viruses target the skin. From an evolutionary perspective, CRPV and HPV1a could have diverged recently, or they could have converged due to their similar target. CRPV is a member of the papillomaviruses so it is related to all viruses in this family (Giri et. al 1985).

Tropism

Rabbit with Shope papillomavirus infection.

Infection of a rabbit’s follicular cell, often occurs in locations including ears, nose, eyelids, and the anus. The infection first appears as a red and swollen area on the skin, followed by development of circular papilloma warts and keratinized horny warts. Although transmission between rabbits is high, the tumors themselves do not contain the infectious virus. 25% of Papilloma infections become malignant and form squamous cell carcinoma. Metastases can form in the lungs and lymph nodes, and if it advances further, can develop in the kidneys and the liver (Praag et. al 2003).

Rabbit Papilloma displays tropism for the cutaneous epithelium. Warts are made up of nearly homogenous vertical tissue strands. Their outer coloration is typically black or greyish, and cut sections are usually white or pinkish white with a flesh-like center. Dark coloration is due to abundant melanin pigment. The warts are made up of several tight, branching, threadlike epidermis processes connected by narrow tissue cores. These growth structures indicate that the growth occurs simultaneously at several different centers, causing the surrounding tissue to bulge from the growth’s lateral pressure. The normal epithelium abruptly transitions into a narrow zone of rapidly thickening epithelial layers, made up of rapidly multiplying cells (Shope et. al 1933).

Rabbits re-infected with the virus exhibit some or complete immunity, and can transmit the virus to other wild rabbits, and from wild to domestic rabbits. A domestic strain cannot transmit to another domestic rabbit, however (Shope et. al 1933).

Immunologically, the papillomatosis virus is not related to fibroma or myxoma in rabbits (Shope et. al 1933).

See also

Oncovirus (cancer virus)

References

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