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At least 307 records · Page 17Linked to original sources
PubMed1986

The epizootics of Kyasanur Forest disease in wild monkeys during 1964 to 1973.

In the Kyasanur Forest disease area two species of wild monkeys, Presbytis entellus and Macaca radiata, succumb to the natural infection with Kyasanur Forest disease (KFD) virus (family Flaviviridae). Between October 1964 and September 1973, 1046 monkeys (860 P. entellus and 186 M. radiata) died. Of these, KFD virus was isolated from 118 P. entellus and 13 M. radiata. Maximum mortality of monkeys was reported during December through May coinciding with the season of activity of immature stages of Haemaphysalis ticks, incriminated vectors of KFD. The epizootic showed an initial spread of the disease to the areas contiguous with the original focus of infection. This was followed by the recognition of epizootics and epidemics in three new foci, removed from the original focus, by the end of 1973. It was also observed that, in certain localities in the original focus, KFD virus activity persisted over several years.

Animals↗
PubMed1988

Molecular cloning and characterization of the DNA of two papillomaviruses from monkeys.

Benign and malignant lesions from monkeys were analyzed for the presence of papillomavirus (PV) DNA. By hybridization with different PV DNA probes under conditions of lowered stringency, two tumors were found to contain PV-specific DNA sequences: (1) a cutaneous papilloma from a Colobus monkey; and, (2) a lymph node metastasis of a squamous cell carcinoma of the penis from a Rhesus monkey. Analysis of the DNA of the papilloma from the Colobus monkey indicated the presence of extrachromosomal DNA whereas analysis of DNA from the Rhesus tumor suggested the presence of integrated viral DNA. The physical size (7.8 and 8.1 kb), colinear alignment to HPV-5, and cross-hybridization with other PV types under low stringency indicate that the two genomic DNA clones represent new PV types that have been tentatively designated as Rhesus papillomavirus type 1 (RhPV 1) and Colobus guereza papillomavirus type 2 (CgPV 2). A putative viral-host DNA junction fragment was also isolated from the Rhesus genomic library. Nucleotide sequences very closely related to RhPV 1 were observed by in situ hybridization in a laryngeal carcinoma from the Colobus guereza monkey. This report communicates the finding of novel papillomaviruses associated with a benign cutaneous tumor and genital and laryngeal malignancies in non-human primates which may have significance as a putative system for the study of papillomavirus-induced genital and laryngeal malignancies in humans.

Animals↗
PubMed1988

Factors limiting the postnatal development of visual acuity in the monkey.

A major factor underlying the prolonged postnatal improvement of visual acuity in primates is an increase in the sampling limit imposed by the photoreceptor mosaic, which may be as much as 5-fold. Further factors operating peripheral to neurons of the lateral geniculate nucleus, which might include changes in neural connectivity, appear to contribute at most 1.5 octaves, between 3 weeks and 6 months of age. Neural factors at the geniculo-cortical synapse may add another half-octave between 10 weeks and 1 yr. Factors operating after the level of the striate cortex (changes in spatial degradation, attention, motivation, etc.) contribute up to another octave or more to the increase in behavioural acuity between birth and about 11 weeks of age. The foveal image is substantially undersampled in young animals and therefore aliasing could occur over a wide range of spatial frequencies.

Animals↗
PubMed1992

Spondyloarthropathy as an Old World phenomenon.

The presence of spine and sacroiliac involvement and the nature and distribution of erosive lesions allowed definitive diagnosis of spondyloarthropathy in the great apes (Gorilla and Pan [chimpanzee]), the lesser ape (Hylobates), and Old World monkeys (Theropithecus, Papio, Cercopithecus, Macaca, Colobus, Presbytis, and Erythrocebus). Analysis of lesional character, distribution, radiological appearance, and sex ratios showed a picture indistinguishable from human spondyloarthropathy. This contrasts with orangutans (Pongo), who lack reactive bone or sacroiliac involvement. A different pathophysiology, as yet undefined, is implied for their erosive arthritis. Limited individual susceptibility to spondyloarthropathy in humans (1% to 4%), Old World monkeys (2.4%), and lesser apes (2.4%) contrasts with the high frequency of disease in the great apes (20% to 28%). The wide geographic distribution of this phenomenon suggests an African and perhaps Asian "panendemic." This natural disease state provides a unique model for in-depth analysis of the contribution of genetic and environmental factors to disease pathophysiology.

Animals↗
PubMed1980

Behavioural and endocrine effects of naltrexone in male talapoin monkeys.

The effect of treating captive male talapoin monkeys with naltrexone hydrochloride (500 micrograms/kg intra-muscular injection twice daily) was studied both in socially living and singly caged animals. The behaviour of the group males and endocrine changes in all treated animals were monitored during the course of treatment and on drug withdrawal. Naltrexone significantly reduced sexual behaviour in previously active males, while increasing grooming interactions. Aggressive behaviour did not change. There was an overall significant elevation in testosterone, LH and cortisol during drug treatment and a significant decrease on withdrawal. Changes in prolactin in response to naltrexone depended upon the pre-treatment level of this hormone: in males in which levels were low, there was a significant elevation in prolactin, while in those with high pre-treatment prolactin, levels were unchanged by the drug. The behavioural changes reported for this primate are in direct contrast to changes reported in rodents, while the hormonal changes, except for prolactin, are comparable to others reported.

Aggression↗
PubMed1982

Opiate antagonists stimulate affiliative behaviour in monkeys.

The effects of treating captive talapoin monkeys acutely (twice daily for 7 days) with naltrexone hydrochloride (0.25 mg 0.5 mg and 1 mg/kg intramuscular injections twice daily), naloxone hydrochloride (0.5 mg/kg IM twice daily) and sulpiride (1.5 mg/kg IM twice daily) was studied in social pairs and singly caged animals. The behaviour of social pairs and endocrine changes in all treated monkeys were monitored before, during and after withdrawal of the course of drug treatment. Naltrexone and naloxone, but not sulpiride, significant increased grooming and grooming invitations while aggressive behaviour, self grooming, scratching and general locomotor activity were unaffected. There was an overall increase in LH, testosterone and cortisol in plasma samples taken 60 mins after opiate receptor blockade. Prolactin was unchanged but increased dramatically in animals treated with sulpiride. No significant endocrine changes were observed to precede the increased grooming behaviour which opiate receptor blockade induced. The behavioural changes reported for this primate support the view that positive affect arising from social bonds may be mediated by cerebral endorphin containing systems.

Animals↗
PubMed1990

Evolution of the pseudoautosomal boundary in Old World monkeys and great apes.

Mammalian sex chromosomes are divided into sex-specific and pseudoautosomal regions. Sequences in the pseudoautosomal region recombine between the sex chromosomes; the sex-specific sequences normally do not. The interface between sex-specific and pseudoautosomal sequences is the pseudoautosomal boundary. The boundary is the centromeric limit to recombination in the pseudoautosomal region. In man, an Alu repeat element is found inserted at the boundary on the Y chromosome. In the evolutionary comparison conducted here, the Alu repeat element is found at the Y boundary in great apes, but it is not found there in two Old World monkeys. During the evolution of the Old World monkey and great ape lineages, homology between the sex chromosomes was maintained by recombination in the sequences telomeric to the Alu insertion site. The Alu repeat element did not create the present-day boundary; instead, it inserted at the preexisting boundary after the Old World monkey and great ape lineages diverged.

Animals↗
PubMed1993

Real and imagined clinicopathological limits of "prion dementia".

The term "prion dementia" has been proposed to replace "spongiform encephalopathy", to accommodate the existence of atypical forms of these "prion protein" (PrP) cerebral amyloidoses that may not show spongiform changes in the brain. We tested brain tissue extracts for the presence of PrP from 46 cases (including 13 familial cases) of non-spongiform dementias with a variety of associated neurological signs, referred to our laboratory for primate transmission studies. None of the cases transmitted disease to primates, and none had PrP detectable by western immunoblots of extracted brain tissue. We conclude that prion dementias are not lurking undetected within the larger landscape of neurodegenerative disorders, and that their clinicopathological limits are, except for a small number of previously reported familial cases, essentially those of spongiform encephalopathy.

Adult↗
PubMedDate not supplied

An analysis of the correlation of lesion size, localization and behavioral effects in 283 published studies of cortical and subcortical lesions in old-world monkeys.

The present article evaluates the quality and magnitude of the effects of lesion size and location and their interaction, on the behavioral performance of old world monkeys by a quantitative comparison of 283 published studies. The results indicate that lesion size alone is a poor predictor of the behavioral performance of monkeys, as opposed to Lashley's work in rats. Lesion location is a reliable predictor of the behavioral performance for brain regions thought to be primarily involved in a specific behavior; however, similar behavioral effects, although less reliable, can be observed for many different lesion loci, suggesting a specialized and a holistic brain functioning to be working at the same time. Some lesion loci are, in sharp contrast to current hypotheses about functional localization in the brain, not associated with impairments, but with significant improvements of a specific behavior. For such lesion loci the correlation of lesion size and behavioral performance may yield significant positive relationships (that is, increasing behavioral improvement with increasing lesion size); these relationships are contrasted by the significant negative relationships obtained for lesions of brain regions thought to be primarily involved in a given behavior. Thus, the lesion size may be a good predictor of the behavioral performance, depending on the lesion location and on the behavior under measurement. The behaviors analysed in this study were discrimination or delayed reaction or delayed matching-to-sample. The former two behaviors involve habit-like learning and are thought to be mediated by corticostriate functional pathways in the brain and the latter behavior implies the learning of single events, being thought to be mediated by corticolimbic functional pathways in the brain. Improved performances were observed for habit-like behaviors after lesions of brain regions (lateral frontal, premotor/motor, parietal, inferotemporal cortex, amygdala and fornix) being not primarily involved in a given behavior but possibly being able to inhibit the corticostriate pathways. Interestingly, lesions of subareas of the neostriatum were found to cause impairments in habit-like behaviors presumably being processed via these subareas (e.g. head of the caudate nucleus and delayed reaction), but to cause significant improvements in other behaviors (e.g. head of the caudate nucleus and visual discrimination). Thus, it may be concluded that diverse systems of functionally interconnected brain regions may maintain reciprocal inhibitions, with the result that a lesion within one system not only leads to a loss of one behavior, but in addition leads to a modification, may be a facilitation, of another behavior.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1983

Hemolytic complement measurement in eleven species of nonhuman primates.

A microtiter system was used to measure hemolytic complement levels in serum from eleven nonhuman primate species. The species studied were Macaca mulatta (rhesus macaque), Macaca radiata (bonnet macaque), Macaca nemestrina (pig-tailed macaque), Macaca fascicularis (crab-eating macaque), Macaca speciosa (stumptailed macaque), Papio cynocephalus (yellow baboon), Papio anubis (olive baboon), Cercopithecus aethiops (African green monkey), Aotus trivirgatus (owl monkey), Ateles fusceps robustus (spider monkey), and Galago crassicaudatus panganiensis (thick-tailed galago). The optimal hemolytic complement titer of the various nonhuman primate species was found to vary with different species sources of erythrocytes and anti-erythrocyte reagents used in the assay. No single erythrocyte and anti-erythrocyte test reagent produced optimal titers for all of the primate species examined. Sera from several species was found to have high spontaneous lytic activity towards non-sensitized sheep erythrocytes which for six species (M. mulatta, M. radiata, M. speciosa, P. cynocephalus, P. anubis and A. trivirgatus) was equal to the titer for antibody sensitized erythrocytes. Evidence of alternate pathway complement activation as a possible reason for the high titer of lytic activity towards unsensitized erythrocytes could not be demonstrated for any nonhuman primate species. In one species, M. mulatta, the sensitizing activity of normal serum for sheep erythrocytes was shown to be in the IgM containing fraction obtained with gel filtration and to be absorbed by boiled sheep erythrocyte stroma which contains Forssman antigen.

Animals↗
PubMed1988

Identification of Plasmodium knowlesi erythrocyte binding proteins.

Plasmodium knowlesi, a malaria of Old World monkeys, invades all Duffy blood group positive human erythrocytes and various New World monkey erythrocytes except Cebus apella. We had previously identified a 135 kDa parasite protein in supernatants of P. knowlesi cultures that bound to Duffy positive but not to Duffy negative human erythrocytes [Haynes et al., J. Exp. Med. 167, 1873-1881 (1988)]. We now use New World monkey erythrocytes as a reagent to identify P. knowlesi proteins in culture supernatants that will bind to all New World monkey erythrocytes susceptible to invasion but not to C. apella erythrocytes, which are refractory to invasion. The 135 kDa protein binds to all New World monkey erythrocytes, including C. appella. Another protein of 155 kDa binds to all New World monkey erythrocytes except C. apella. The 155 kDa protein binds to Old World monkey erythrocytes, the natural host of P. knowlesi; it does not bind to human Duffy positive erythrocytes. This and the previous study are the beginning of the identification of parasite proteins of P. knowlesi that bind to erythrocytes in a receptor specific manner.

Animals↗