Cats And Dogs

Cats And Dogs
Real
Cats Are The True "Best Friend" Of Humanity
2R62
1994/02/24
Dogs and Cats
FIV
FAIDS
AIDS
HIV
Man's Best Friend
Radio
Antigravity, The Feline Butterology Theory

Author:
Bryan J. Maloney

Date:
1994/02/24


Humans, the dominant species of the planet Sol III, Orion Arm, are remarkably less intelligent than their apparently ascendent status might lead one to believe. Take, for example the common human phrase "Dog is man's best friend." First, this phrase is quite misleading in its choice of words, as any rational reader would come to the conclusion that this "dog" (canis domesticus L.) is somehow preferentially attracted to adult males of the human species. Nothing could be further from the truth, as "Man" in this case is meant to mean all members of the species homo sapiens regardless of their gender or age. The fact that humans seem not to be in the least bit perturbed by this linguistic blunder only underscores the species's general lack of good sense.

However, this is not the only way in which the human mind is capable of enshrining lack of intelligence. The fact that this particular statement is repeated so often and is so often believed is proof positive that something behind the scenes, as it were, must be going on to place humans in their role on their home planet.

For dispassionate examination of the situations of humans and other creatures would lead one to believe that dogs, while individually often on friendly terms with humans, are as a collective not as friendly as might be supposed. For example, it is well known, even among humans, that a common source of the dangerous disease "rabies" is a bite from an infected dog. Dogs are also common carriers of parasites dangerous to humans. While many might dismiss these facts as "coincidences," an observer might come to the conclusion that what appears to be "friendship" on the part of "dog" towards "man" may, in fact, be a cunning species-wide ingratiation program.

What species, then, would better qualify as the "best friend" of humanity? Recent discoveries made by the humans leads one to believe that the "cat" (felis catus, L.) may better deserve this title. The reason for this conclusion is that humanity found itself confronted with a very perplexing and fatal medical disorder, which they named "AIDS" (although it only "aids" humans in their progress towards the grave). This syndrome was characterized in the early-to-middle 1980s ("AD" Terran annuation system) and was ultimately assigned to be an eventual result of a virus that was given the name "human immunodeficiency virus" or HIV.

Feline immunodeficiency virus (FIV) is the causative agent of a feline acquired immune deficiency syndrome (FAIDS) that was discovered in 1986 in southern California (Pedersen et al, 1987; Yamamoto et al, 1988). The associated infection tends to have a long asymptomatic seropositive stage followed by clinical illness. Clinical signs include fever, lymphadenopathy, diarrhea, wasting, opportunistic infection, neurological disorder, and neoplasia, especially lymphoma, myoproliferative disease, and various cytopenias including anemia, lymphopenia, and leukopenia (which may not be due to the activity of FIV alone) neoplasia, especially lymphoma and myoproliferative disease, (Hutson et al, 1991; Moraillon et al, 1992; Pedersen et al, 1989a, b; Shelton et al 1991). Neoplastic effects of HIV infection seem to be enhanced with concurrent FeLV infection (Hutson et al, 1991; Shelton et al 1991).

Clinical immunological effects include inversion of neutrophil to lymphocyte cell ratio (Moraillon et al, 1992), probably due to preferential infection of CD4 cells over CD8 cells, as clinical studies demonstrated a reduction in CD4 but not CD8 lymphocytes (Tompkins, et al, 1991; Ackley et al, 1990; Barlough, et al, 1991, Hoffmann-Fezer et al, 1992). Interestingly, unspayed seropositive female cats showed significantly higher CD4 counts and CD4/CD8 ratios than did males or spayed females (Hoffmann- Fezer et al, 1992). In vitro studies have demonstrated that FIV infected CD4 and CD8 T-lymphocytes and macrophages. However, different isolates showed different relative affinities for each type of cell (Brown et al, 1991, Tokunaga et al, 1992). Macrophage function is also altered in vitro in FIV infection (Lin and Bowman 1992). Isolates of FIV have shown differences in vitro for adaptability to various cell lines and cell-type tropisms (Kawaguchi, et al, 1991).

FIV has been found on five continents (Bandecchi et al, 1992; O'Connor et al, 1991; Olmstead et al, 1992; Sukura et al, 1992; Yamamoto et al, 1989). Percentages of infection range from 7.4%-8% in indoor pets and 25% in free-roaming cats in the United States (O'Conner et al, 1991; Yamamoto et al, 1989), 24% in free-roaming cats in Italy (Bandecchi et al, 1992), and 6.8% in Finland for free-roaming cats (Sukura et al, 1992). Feline leukemia virus (FeLV) infection appears to accompany FIV infection in a large percentage of these cases (Bandecchi et al, 1992; O'Connor et al, 1991; Olmstead et al, 1992; Sukura et al, 1992; Yamamoto et al, 1989). In wild feline species, seropositivity to FIV or FIV-related viruses is as high as 80%. However, these free-ranging large cats appear to be free of pathologic signs (Olmstead et al, 1992).

Protein studies (Steinman et al, 1990, Kiyomasu et al, 1991) sequence analysis (Olmstead et al, 1989), and deletion mutant analysis (Morikawa and Bishop, 1992) demonstrate that FIV is a lentivirus (the same viral sub- family which contains HIV) in that it possesses the classical lentivirus genome arrangement of a 5' long terminal repeat, rev, gag, pol, and env genes with small open reading frames (vif, etc.) between the pol and env genes (Clements and Wong-Stall, 1992, Coffin, 1990; Narayan and Clements, 1990). However, genome arrangement and phylogenetic analysis of various gene products indicate a closer genetic relationship to the ungulate lentiviruses than to currently identified hominoid (human and simian) immunodeficiency viruses (Olmstead et al, 1989, 1992).

Nevertheless, clinical signs of FIV infection are closer to those of the hominoid viruses in their native hosts than to the ungulate viruses in their native hosts (Fenner et al, 1987).

While work is going on to elucidate the disease mechanisms for HIV, the information to be derived from this work, however valuable, will be limited by the fact that an adequate animal model that manifests clinical signs similar to human AIDS has yet to be discovered or engineered for HIV. FIV, on the other hand, produces a clinical syndrome much like human AIDS (CDC, 1987; Hirsch and Curran, 1990). Elucidation of the pathways of FIV pathogenesis could permit design of drugs to block these pathways that could then be more readily tested upon animals manifesting clinical disease than could drugs derived from work directly upon HIV. Furthermore, domestic cats are cheaper and easier to care for than are chimpanzees and maqacques currently used for HIV and HIV-related research (not to mention the fact that felis catus is hardly an endangered or threatened species). It is true that the somewhat distant relationship between FIV and HIV might pose some difficulties in directly transporting data back and forth. However, using FIV as a model for the human disease will better permit workers to gauge problems such as relative host toxicity of treatments derived from information on assembly and packaging, collateral non-toxic host effects of such treatments, etc. with more confidence than permitted by the limited trials in animals that do not manifest immune deficiency signs.

Now, one would think that the "best friend" of "man" would have leapt into the breach and developed a disease that could have been used to model such a feared human malady. However, it seems that the much-maligned cat has instead taken this role. Perhaps humanity might prove some vestige of intelligence if they are able to take notice of this noble self-sacrifice on the part of this small animal.

References

Ackley, C.D., Yamamoto, J.K., Levy, N., Pedersen, N.C., Cooper, M.D. 1990.
  Immunologic abnormalities in pathogen-free cats experimentally infected
  with feline immunodeficiency virus. J. Virol. 64:5652-5655
Bandecchi, P., Matteucci, D., Baldinotti, F., Guidi, G., Abramo, F.,
  Tozzini, F., and Bendinelli, M. 1992. Prevalence of feline
  immunodeficiency virus and other retroviral infections in sick cats in
  Italy. Vet. Immunol. Immonopath. 31:337-345
Brown, W.C., Bissey, L., Logan, K.S., Pedersen, N.C., Elder, J.H., and
  Collison, E.W. 1991. Feline Immunodefieincy virus infects both CD4+ and
  CD8+ T lymphocytes. J. Virol. 65:3359-3364
CDC. 1987. Classification system for human T-lymphotropic virus type
  III/lymphadenopathy-associated virus infections. MMWR. 35:334-339.
Clements, J.E., and Wong-Stall, F. 1992. Molecular biology of lentiviruses
  (review). Seminars in Virology. 3:137-146.
Coffin, J.M. 1990. Retroviridae and their replication (review). In Fields,
  B.N., and Knipe, D.M. (ed) Virology. pp 1437-1489. Raven Press. New York.
Fenner, F., Bachmann, P.A., Gibbs, E.P.J., Murphy, F.A., Studdert, M.J.,
  White, D.O. 1987. Diseases caused by lentiviruses. In Veterinary Virology,
  pp569-576. Academic Press, Inc. New York.
Hoffmann-Fezer, G., Thum, J., Ackley, C., Herbold, M., Mysliwietz, J.,
  Thefeld, S., Hartmann, K., and Kraft, W. 1992. Decline in CD4+ cell
  numbers in cats with naturally acquired feline immunodeficiency virus
  infection. J. Virol. 66:1484-1488
Hutson, C.A., Rideout, B.A., and Pedersen, N.C. 1991. Neoplasia associated
  with feline immunodeficiency virus infection in cats of southern
  California. JAVMA. 199:1357-1362
Kawaguchi, Y., Maeda, K., Tohya, Y., Furuya, T., Miyazawa, T., Horimoto, T.,
  Norimine, J., Kai, C., Mikami, T. 1992. Replicative differences in early-
  passage feline brain cells among feline immunodeficiency virus isolates.
Kiyomasu, T., Miyazawa, T., Furuya, T., Shibata, R., Sakai, H., Sakuragi, J-
  I., Fukasawa, M., Maki, N., Hasegawa, A., Mikami, T., and Adachi, A. 1991.
  Identification of feline immunodeficiency virus rev gene activity. J.
  Virol. 65:4539-4542
Lin, D-S., and Bowman, D.D. 1992. Macrophage functions in cats
  experimentally infected with feline immunodeficiency virus and Toxoplasma
  gondii. Vet. Immunol. and Immonopath. 33:39-78
Moraillon, A., Barre-Sinoussi, F., Parodi, A., Moraillon, R., and Dauguet,
  C. 1992. In vitro properties and experimental pathogenic effect of three
  strains of feline immunodeficiency viruses (FIV) isolated from cats with
  terminal disease. Vet. Microbiol. 31:41-54
Morikawa, S., and Bishop, D.H.L. 1992. Identification and analysis of the
  gag-pol ribosomal frameshift site of feline immunodeficiency virus.
  Virology. 186:389-397
Narayan, O. and Clements, J.E. 1990. Lentiviruses (review). In Fields, B.N.,
  and Knipe, D.M. (ed) Virology. pp 1571-1585. Raven Press. New York.
O'Connor, T.P., Tonellin, Q.J., and Scarlett, J.M. 1991. Report of the
  national FeLV/FIV awareness project. JAVMA. 199:1348-1353
Olmstead, R.A., Hirsch, V.A., Purcell, R.H., and Johnson, P.R. 1989.
  Nucleotide sequence analysis of feline immunodeficiency virus: genome
  organization and relationship to other lentiviruses. Proc. Natl. Acad.
  Sci. USA. 86:8088-8092
Olmstead, R.A., Langley, R., Roelke, M.E., Goeke, R.M., Adger-Johnson, D.,
  Goff, J.P., Packer, C., Laurenson, M.K., Caro, T.M., Scheepers, L., Wildt,
  D.E., Bush, M., Martenson, J.S., and O'Brien, S.J. 1992. Worldwide
  prevalence of lentivirus infection in wild feline species: epidemiologic
  and phylogenetic aspects. J. Virol. 66:6008-6018.
Pedersen, N.C., Ho, E.W., Brown, M.L., and Yamamoto, J.K. 1987. Isolation of
  a T-lomphotrophic virus from domestic cats with an immunodeficiency-like
  syndrom. Science. 253:790-793
Shelton, G.H., Linenberger, M.L., and Abkowitz, J.L. 1991. Hematologic
  abnormalities in cats seropositive for feline immunodeficiency virus.
  JAVMA. 199:1353-1357
Steinman, R., Dombrowski, J. O'Connor, T., Motelaro, R.C., Tonelli, Q.,
  Lawrence, K., Seymour, C., Goodness, J., Pedersen, N.C., and Andersen,
  P.R. 1990. Biochemical and immunological characterization of the major
  structural proteins of feline immunodeficiency virus. J. Gen. Virol.
  71:701-706
Sukura, A., Salminen, T., and Lindberg L.A. 1992. A survey of FIV antibodies
  and FeLV antigens in free-roaming cats in the capital area of finland.
  Acta. Vet. Scand. 33:9-14
Tokunaga, K., Nishini, Y., Oikawa, H., Ishihara, C., Mikami, T., and Ikuta,
  K. 1992. Altered cell tropism and cytopathology of feline immunodeficiency
  viruses in two different feline CD4-Positive, CD8-negative cell lines.
Tompkins, M.B., Nelson, P. D., English, R.V., and Novotny, C. 1991. Early
  events in the immunopathogenesis of feline retrovirus infections. JAVMA.
  199:1311-1315
Yamamoto, J. K., Ackley, C.D., Zochlinski, H., Louie, H., Pembroke, E.,
  Torten, M., Hansen, H., Munn, R., Okuda, T. 1991. Development of IL-2
  independent feline lymphoid cell lines chronically infected with feline
  immunodeficiency virus: importance for diagnostic reagents and vaccines.
  Intervirology. 32:361-375.
Yamamoto, J.K., Okuda, T., Ackley, C.D., Louie, H., Pembroke, E.,
  Zochlinski, H., Munn, R.J., and Gardner, M.B., 1991. Experimental vaccine
  protection against feline immunodeficiency virus. AIDS Res. Hum. Retrovir.
  7:911-921.

See also

Subtitle: 
Cats Are The True "Best Friend" Of Humanity
Factuality: 
Real
PGG Author: 
Bryan J. Maloney
PGG Number: 
2R62
PGG Index: 
Man's Best Friend
PGG Date: 
1994/02/24
PGG Xref: 
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