key: cord-007923-j3jpqd7k
authors: O'Brien, Stephen J.
title: Cats
date: 2004-12-14
journal: Curr Biol
DOI: 10.1016/j.cub.2004.11.017
sha: 
doc_id: 7923
cord_uid: j3jpqd7k

nan

ecological niches on every continent except Australia and the poles. Wild cats dominate their habitat but require vast expanses to survive, which explains the tragic depredation such that every species of Felidae, except the domestic cat, is considered either endangered or threatened in the wild today by CITES, IUCN Red Book and other monitors of the world's most endangered species.

There are lots of them, small and easy to keep in the laboratory. Whether we love cats or hate them, biology has learned much from studies of their comparative anatomy, comparative physiology (notably neurology) and behavior. For many biological subdisciplines, the 36 cat species are considered as three groups: large, medium and small, a testament to their amazing similarity.

The exception is reproduction, where each species has evolved exquisite co-adapted strategies for ovulation, hormone level regulation, sperm production, estrous incidence, mating preference and social organization. Scrutiny by behavioral ecologists has provided a rich literature of distinctive reproductive parameters for several cat species, facilitating advances in assisted reproduction such as artificial insemination, cryopreservation, embryo transfer, in vitro fertilization and the first cloning of a domestic cat in 2002. The advanced stage of reproductive assessment will one day soon lead to feline embryonic stem cells, transgenic and gene knockout cats, and protocols for stem cell and gene therapy trials.

One of the most powerful biomedical models for cats involves the interaction of deadly infectious agents and the cat host's genome. Domestic cats first gave us feline leukemia virus, which allowed the discovery of scores of 'oncogenes' in the 1970s and 1980s. When homologous human oncogenes were rapidly discovered thereafter, their misfiring in signal transduction pinpointed the molecular basis for many aggressive cancers. More recently, feline immunodeficiency virus (FIV), a first cousin of HIV, was discovered in house cats as the cause of a depletion of the CD4 T-cell subset that is a prelude to immune system collapse and pathology, the only naturally occurring model of AIDS. Interestingly, over eight free-ranging wild species of Felidae are infected with their own species-specific FIV strain (based on FIV gene sequence monophyly) that in most cases seems to be attenuated by historic selection of genetically resistant survivors in today's wild places. The devastating SARS human coronavirus has a feline counterpart that causes a deadly feline infectious peritonitis (FIP) syndrome in domestic cats. An outbreak of FIP in a genetically uniform African cheetah colony led to 100% morbidity and 60% mortality, emphasizing the sensitivity of genetically inbred hosts to viral outbreaks.

Cats and their wild relative have given some sobering lessons about emerging virus outbreaks. In the mid 1970s, a feline pan-leucopenia virus cultivated in a cat vaccine factory abruptly jumped from cats to dogs, producing a hyper-virulent A Persian breed domestic cat. (Photo courtesy of M. Calingo). strain in puppies that within a few months caused widespread puppy mortality across the world. Payback from the dogs came when a strain of canine distemper, endemic in the pet dogs of Masai tribesman in Tanzania, jumped to hyenas and then to African lions, killing a third of the huge lion population of Serengeti National Park in a six month interval in 1994.

Add to the list of verified catspecific agents: alpha-herpesvirus, toxoplasmosis, cryptococcus, plague, Q-fever, chlamydiosis and rotavirus infections, ehrlichiosis, calicivirus infection, poxvirus infection and mycobacteriosis. Cats are also highly resistant to anthrax, with obvious implications. All these infections, and more, could prove valuable to biomedical research, providing we have a better working knowledge of the innate and adaptive immune system of cats.

Domestic cats and dogs enjoy more medical scrutiny than any species except humans. The world's veterinary schools produce thousands of practitioners each year, providing extensive documentation of genetic and chronic diseases with relevance to human maladies. The result is a comprehensive veterinary literature, which has described some 258 feline genetic diseases (http://www.angis.org.au/Databa ses/BIRX/omia/). These disease models offer, not only insight into disease development, but opportunities for better diagnostics and treatment experimentations.

Institute (NHGRI) announced its decision to support sequencing of the domestic cat genome, along with those of seven other species: elephant, armadillo, tenrec, common shrew, guinea pig, hedgehog and rabbit. These species were chosen to complement those already selected for whole genome sequencing (human, mouse, rat, cow, chimpanzee, macaque, opossum and platypus) and to reflect the diversity among the 4500 living species of mammals as a first step in annotating the human genome's largely uninterpreted coding, regulatory and evolutionary conserved sequences. The cat offers the promise of a second carnivore species (in addition to the dog, which shares a common ancestor with cats dating back to approximately 60 million years ago) to improve human genome annotation, as well as to complement the biomedical and genomic discoveries that make the feline genome attractive.

Genome evolution in mammals appears to proceed at two very different rates. The common default rate of chromosomal exchange is very slow and deliberate, so that the genome organization can be inferred for the common ancestor of all primates, carnivores and placental mammals. But a more rapid mode of genome rearrangement is seen in some lineages, such as gibbons, owl monkeys, dogs, bears and murid rodents, the genomes of which appear to have been re-shuffled several times relative to the ancestral form. Cats and humans both have genomes in the primitive, un-rearranged form, so the cat provides a good opportunity to study the constraints on genome organization that have characterized the 105 million year old mammalian radiations. The conserved genome of the cat is retained in the other 36 Felidae species, as well as most of the 246 species of the Carnivora order, the only reshuffled exceptions occuring in the dog and bear families.

What can we expect after the cat genome sequence becomes available? Many areas of biological and medical research will benefit from the projected cat genome sequence. Human genome interpretation and annotation will be augmented by, on average, a single variant for each of its three billion base pairs. Cats will enjoy genomic tools for inspection of feline hereditary disease, as well as the discovery of candidate gene variants that may explain evolved genomic defenses of infectious disease that threaten cats and man. Evolutionary biologists will identify specific genes contributing to survival and species formation as unabridged gene/sequence maps narrow the search for adaptations. The observed constraints on genome reorganization will become a challenge for inferring the footprints of evolutionary steps that led to the modern cat species. An increased and informed database of mechanistic developmental specializations will add yet another reason to conserve the surviving cat species that are the keystone of species and habitat conservation projects, from cheetahs in Namibia, to tigers in India and the Russian far east, to lions in east Africa and jaguars in the Amazon.

The Natural History of the Wild Cats

The Laboratory Cat

Wild Cats Status Survey and Conservation Action Plan IUCN Gland Switzerland

Tears of the Cheetah and Other Tales from the Genetic Frontier

The promise of comparative genomics in mammals

The Feline Genome Project

Wild Cats of the World