Mhc-DRB diversity of the chimpanzee (Pan troglodytes)

Fifty-four chimpanzee Patr-DRB and five human HLA-DRB second exons were cloned and sequenced from thirty-five chimpanzees and four B-cell lines and compared with known Mhc-DRB sequences of these two species. Equivalents of the HLA-DRB1 ^* 02,-DRB1 ^* 03, -DRB1 ^* 07 allelic lineages and the HLA-DRB3,-DRB4, -DRB5, -DRB6, and -DRB7 loci were all found in the chimpanzee. In addition, two chimpanzee Patr-DRB lineages (Patr-DRBX and -DRBY) were found for which no human counterparts have been described. None of the Patr-DRB sequences is identical to known HLA-DRB sequences. The Patr-DRB1 ^* 0702 and HLA-DRB1 ^* 0701 alleles are the most similar sequences in a comparison between the two species and differ by only two nucleotides out of 246 sequences. Equivalents of the HLA-DRB1 ^* 01,-DRB1 ^* 04, and -DRB1 ^* 09 alleles were not found in our sample of chimpanzees. A per locus comparison of the number of Patr-DRB alleles with the HLA-DRB alleles shows that the Patr-DRB3, -DRB4, -DRB5, and -DRB6 locus are, thus far, more polymorphic than ther human homologs. The polymorphism of the Patr-DRB1 locus seems to be less extensive than that reported for the HLA-DRB1 locus. Nevertheless, the Patr-DRB1 locus seems to be the most polymorphic of the Patr-DRB loci. Phylogenetic analyses indicate that the HLA-DRB1 ^* 09 allele may have originated from a recombination between a Mhc-DRB5 allele and the DRB1 allele of a Mhc-DR7 haplotype. Although recombination seems to increase the diversity of the Patr-DRB alleles, its contribution to the generation of Patr-DRB variation is probably low. Hence, most Patr-DRB diversity presumably accumulated via recurrent point mutations. Finally, two distinct PAtr-DRB haplotypes are deduced, one of which (the chimpanzee equivalent of the HLA-Dr7 haplotype) is probably older than 6–8 million years.The nucleotide sequence data reported in this paper have been submitted to the GenBank nucleotide database and have been assigned the accession numbers Mg6074-Mg6132. Correspondence to: M. Kenter.     

Acute appendicitis in a chimpanzee (Pan troglodytes)

BACKGROUND: A 7-year old, female chimpanzee (Pan troglodytes) developed acute abdominal pain and anorexia. An irregular, mineral opacity was identified in the caudal right quadrant of the abdomen on radiographs and computed tomography scan, which appeared to be in the region of the cecal appendage. RESULTS AND CONCLUSIONS: A diagnosis of acute appendicitis was made based on clinical signs, abnormal haematology findings, and consultation with a human radiologist. Exploratory laparotomy was performed and the cecal appendage was removed. On histologic examination, the mucosal epithelium contained eosinophilic and neutrophilic inflammation. The inflammation extended through the tunica muscularis to the serosal surface and adjacent mesentery. The histologic findings were consistent with acute appendicitis in humans. The chimpanzee recovered well from surgery with immediate improvement in clinical signs and no post-operative complications.     

Perinatal dental development in the chimpanzee (Pan troglodytes)

The synthesis of both ontogenetic and phylogenetic data should provide the ideal explanation of morphologic variation, but for the primate dentition, this has not yet occurred. Information concerning growth and development of primate teeth is lacking, in part because of the paucity of specimens. We have therefore examined the deciduous second molars (dm2) and tooth buds of the permanent first molar (M1) of 12 chimpanzees (Pan troglodytes), aged 6.5 months of gestation to 4 postnatal months. The ordering of cusp calcification was identical to that of other primates. By regression analysis, correlations of mesial and distal widths with buccal, lingual, and mesiodistal lengths were low, most probably because of decreased rates of change (slopes) and the relatively small sample size. Correlations were, however, greater for mandibular than for maxillary dentition and higher for age than for body weight; for both the dm2 and M1, distal moieties increased faster and were more highly correlated with other dental variables and age than were mesial ones. Comparison with data from humans revealed both differences and similarities in the absolute size and growth rate of dental moieties during the perinatal period. As the reasons for ontogenetic variation become understood for individuals, species, and higher taxa, the phylogenetic implications of differential growth should become clearer as well.     

Predation on mammals by the chimpanzee (Pan troglodytes)

With respect to prey selectivity and predation frequency, chimpanzees (Pan troglodytes) show local differences as well as diachronic variability within the same population. When data on predation from three long-term studies at Mahale, Gombe, and Tai are compared, some differences and similarities emerge; Mahale is more like Gombe than Tai in regard of prey selection but features of hunting at Tai with respect to predation frequency are not conspicuous. The most responsible factor for diversity in prey selectivity is a distinct “prey image” maintained by chimpanzees of different populations, although it is necessary to clarify in future studies why and how such tradition develops. Relative body size of chimpanzees to prey species and/or the degree of cooperation among members of a hunting party may explain the variability in prey size selected at each site, the latter influencing the frequency of successful hunts at the same time. Although various degrees of habituation and different sampling methods including artificial feeding might have obscured the real differences, recent data from the three populations do not seem to be biased greatly by such factors. Nevertheless, it is still difficult to make strict comparisons due to the lack of sufficient standardized data across the three populations on the frequency of hunting and predation. It is suggested that the size or demographic trend of a chimpanzee unit-group, especially the number of adult males included, necessarily influences its hunting frequency as well as its prey profile. It is also suggested that factors which bring these males together into a party (e.g. fruit abundance, swollen females, conflict between unit-groups etc.) strongly affect theactual hunting and kill rates. Other possible factors responsible for the local differences are forest structure (e.g. tree height), skilful “hero” chimpanzees, and competition with sympatric carnivorous animals. A total of at least 32 species have been recorded as prey mammals of chimpanzees from 12 study sites and the most common prey mammals are primates (18 species), of which 13 species are forest monkeys. Forest monkeys, colobine species in particular, are often the most common victims of the predation by chimpanzees at each site. We may point out a tendency toward selective hunting for the forest monkeys in terms of the selectivity of prey fauna among all three subspecies of chimpanzees, including populations living in drier environment. The mode of chimpanzee hunting seems to correspond to the highest available biomass of gregarious, arboreal monkeys in the forest, colobine species in particular. In contrast, bonobos (P. paniscus) are less carnivorous than chimpanzees, only rarely preying on a few species of small mammals. The sharp contrast of the two allied species in their predatory tendencies appears to have something to do with the differences in the structure of primary production between their habitats.     

Hyperglycemic hyperosmolar state in a chimpanzee (Pan troglodytes)

A 19-year-old female chimpanzee (Pan troglodytes) presented for cachexia, acute weakness, hyporexia, icterus, and polyuria. The animal was diagnosed with a hyperglycemic hyperosmolar state, which is a well-recognized syndrome in diabetic humans that is rarely diagnosed in animals. This case documents an important and likely under-reported syndrome in non-human primates.     

Spontaneous heart disease in the adult chimpanzee (Pan troglodytes)

Background  A high incidence of heart disease, especially idiopathic cardiomyopathy (IC), is seen in chimpanzees ( Pan troglodytes ).
Methods  We reviewed clinical records and necropsy reports of 87 adult chimpanzees for possible causes of heart disease/IC. We examined age, sex, cause of death, weight, diet, environment, infectious diseases, experimental uses and clinical pathology.
Results  The overall prevalence of heart disease in chimpanzees was 67.81%; the prevalence of IC was 51.72%. The prevalence of IC was significantly higher in males (60.32%) than that in females (29.17%, P  = 0.009). The prevalence of other heart disease was higher in females (25%) than that in males (12.70%, P  = 0.165). Heart failure occurred in 47.13% of chimpanzees. Heart disease was the primary cause of death in 34.49% of chimpanzees; 29.88% died of unknown causes.
Conclusions  We found no evidence that diet, environment, viral agents, experimental use or disease exposure contributed to the deaths resulting from IC in chimpanzees.     

Intracranial arachnoid cysts in a chimpanzee (Pan troglodytes)

An intracranial arachnoid cyst was detected in a 32-year-old, 44.6-kg, female chimpanzee at the Primate Research Institute, Kyoto University. Magnetic resonance imaging (MRI) and computed tomography (CT) were performed and the cognitive studies in which she participated were reviewed. MRI revealed that the cyst was present in the chimpanzee’s right occipital convexity, and was located in close proximity to the posterior horn of the right lateral ventricle without ventriculomegaly. CT confirmed the presence of the cyst and no apparent signs indicating previous skull fractures were found. The thickness of the mandible was asymmetrical, whereas the temporomandibular joints and dentition were symmetrical. She showed no abnormalities in various cognitive studies since she was 3 years old, except a different behavioural pattern during a recent study, indicating a possible visual field defect. Detailed cognitive studies, long-term observation of her physical condition and follow-up MRI will be continued.     

Functional analysis of chimpanzee (Pan troglodytes) private signing

The chimpanzee's use of American Sign Language (ASL) to communicate with humans and with each other has been empirically demonstrated in several reports, but this is the first research to experimentally examine their use of sign language in a nonsocial fashion: private signing. This experiment examined the private signing behavior of five signing chimpanzees, using a remote videotaping technique with no human present. It was found that all five chimpanzees signed to themselves for a total of 368 instances. These instances of private signing were classified into nine different functional categories as has been done in the analysis of private speech and signing in hearing and deaf human children. Similar to humans, a few of the categories accounted for the majority of the instances of private signing. These findings empirically demonstrate a behavior similar to private speech and signing in humans.     

Semen characteristics of the adult male chimpanzee (Pan troglodytes)

The chimpanzee, because of its similarities to the human, is especially valuable in studies of reproductive function. However, relatively little is known about the physiology of reproduction in the adult male chimpanzee. This study provides, for five adult male chimpanzees, baseline values for testicular volume without and with pressure and for cellular and biochemical characteristics of ejaculates collected by artificial vagina (AV). There was no correlation between body weight and testicular volume measured without or with pressure. The ratios of mean testicular volume without and with pressure were not statistically different among animals. Statistical analysis of penetration of denuded hamster oocytes by ejaculated chimpanzee sperm revealed no correlations between sperm count and percentage of eggs penetrated. There was significant variability in concentrations of protein and fructose and in activities of alpha-glucosidase and acid phosphatase among samples from different animals. Computer-assisted motion analysis (CAMA) of sperm provided baseline data on motion parameters necessary for future evaluation of this technique for semen analysis in the chimpanzee. The level of demonstrated inter-animal variation mandates use of each animal as its own control for studies on normal and altered reproductive function. © 1993 Wiley-Liss, Inc.     

Expression of beta-defensin-1 in chimpanzee (Pan troglodytes) airways

In human airways, beta-defensins function in the elimination of various pathogens. They have been identified in a wide range of species. Here we report the identification and expression of chimpanzee beta-defensin-1 (cBD1), which is a homolog of human beta-defensin-1, in chimpanzee airways and skin. The cBD1 cDNA sequence differs by only one synonymous nucleotide substitution compared to the human cDNA sequence. In situ hybridization revealed that in lung tissue beside alveolar macrophages also airway epithelial cells, endothelial cells and type II pneumocytes express cBD1 mRNA. In skin, cBD1 mRNA was expressed in keratinocytes and endothelial cells. Together, these results show similarity in structure and expression pattern and perhaps in function.     

Longitudinal analysis of length growth in the chimpanzee (Pan troglodytes)

The adolescent growth spurt in linear dimension in humans is considered to be unique among mammals, but few comparative studies have been done, even on chimpanzees. Growth of the summed length of crown to rump, thigh, and leg was studied longitudinally in 12 chimpanzees. We took body weight growth and reproductive maturation into consideration. Reproductive maturation was monitored by the swelling of sexual skin and menarche in females, and by testicular development in males. We applied two relationships found in humans between body length growth and the environment to the chimpanzees. The first relationship was the robustness of the growth spurt, meaning that the spurt is absent only in individuals under the most severe environmental pressure. Subjects maturing in a favorable or even mediocre environment are anticipated to show the growth spurt. The second relationship was catch-up growth, where, when the environment is ameliorated, growth may be accelerated to attain the target size. Catch-up growth at the end of the juvenile period may mimic the adolescent growth spurt. Results showed that subjects living under favorable conditions did not exhibit a growth spurt, and that it was only the subjects who had delayed growth in the juvenile period that showed a spurt in adolescence, the period when reproductive maturation occurred. Although we have concluded that chimpanzees do not have an adolescent growth spurt, except in cases of catch-up growth, this does not mean that they have a different growth pattern from that of humans. The absence of a growth spurt may be associated with adaptations to chimpanzee patrilineal society, where adolescent males are incorporated into the adult hierarchy at a low rank.     

Social behavior in a captive chimpanzee (Pan troglodytes) group

A group of captive chimpanzees, consisting of one adult male and three mother/infant pairs, was systematically observed over a 15-month period. Over 200 hr of data were collected, using both sequential and time sampling techniques, and compared to the available data on wild chimps. Unlike many captive groups, most behavior patterns were remarkably similar, both qualitatively and quantitatively, to that of wild chimpanzees including: play, grooming, infant sexual development, tool use, food sharing, prosocial partner preferences, and aggressive displays.     

Rapid changes in chimpanzee (Pan troglodytes) urinary cortisol excretion

Behavioral endocrinologists are aware that many hormones exhibit a diurnal rhythm, and attempt to correct for this pattern by collecting physiological samples only during specified time windows of varying lengths. In studies utilizing urinary measures of hormone levels, this window often spans 2 h or longer. In this study, we compared chimpanzee urinary cortisol levels in sample pairs collected within 1 h of each other in an attempt to validate the use of a time window for sample collection. Chimpanzees were housed at the University of Louisiana New Iberia Research Center and trained to urinate into a paper cup on command; a total of 41 sample pairs were included in this analysis. We found that mean cortisol levels in the two sets of samples, collected within 1 h or less of each other, were significantly different; the mean cortisol level of the first set of samples was significantly higher than that of the second set. This hormone's diurnal pattern of secretion accounts for this significant decrease over a very short time period. We conclude that collection methodologies involving time windows of 1 h or longer need to take into account such rapid changes in levels of excreted hormone. We advocate the use of methodological and statistical corrections to decrease the impact of short-term fluctuations in urinary cortisol.     

Partial hydatidiform mole in a pregnant chimpanzee (Pan troglodytes)

Until now, the occurrence of hydatidiform mole in non-human primates has not been documented. This report presents a case in which a stillborn fetus, associated with a partial hydatidiform mole, was found at necropsy in the uterus of a pregnant chimpanzee (Pan troglodytes) which had suddenly died. Hydropic swelling of the chorionic villi and proliferation of trophoblastic cells were present. The trophoblast was stained enzyme-immunohistochemically with human chorionic gonadotropin (hCG) and pregnancy-specific-β1-glycoprotein (SP1). The concentrations of hCG and SP1 in maternal serum were high, 1,350 mIU/ml and 1,000 ng/ml, respectively. The distribution of DNA content of the cytotrophoblast in the molar villi shifted from diploid to an aneuploid pattern. © 1993 Wiley-Liss, Inc.     

Placental implications for pregnancy complications in the chimpanzee (Pan troglodytes)

Placentas from 28 term chimpanzee pregnancies, including two sets of dichorionic-diamniotic twin-pregnancies, were examined and compared histopathologically with those obtained from 171 small-for-dates (SFD), 306 premature, and 77 pregnancy toxemic human infants. Term infant and placental weights for the chimpanzee were generally smaller than for any of the human categories studied. Macroscopically, the chimpanzee placentas showed a high frequency of extrachorialis, infarctions, intervillous thrombi, and marginal hemorrhages, pathologies frequently associated with pregnancy toxemia and abruptio placenta in the human being. Yet, ultrastructurally, the chimpanzee chorionic villi evidenced well-developed organella, syncytial microvilli, and chorionic capillaries, although villitis and inflammation of the membranes and cord were not infrequently seen. These findings suggest that chimpanzees may suffer the same obstetric complications seen in human pregnancies.     

Multidimensional auditory stimulus control in a chimpanzee (Pan troglodytes)

An adolescent female chimpanzee (Pan troglodytes) was trained to discriminate auditory compound stimuli differing in tonal frequency and/or tone on-off rate. Following acquisition training and overtraining, she was shifted to multidimensional stimulus control testing using redundant relevant auditory stimulus sets with discriminability of elements in each dimension varied systematically. Although the control by both dimensions changed significantly as a function of discriminability, the degree of dimensional control was stronger in the tone on-off rate than in the tonal frequency. These results clearly demonstrated “attentional” control of the chimpanzee's auditory discrimination behavior and the interaction between two dimensions of auditory stimuli. The author is now at the Department of Psychology, Primate Research Institute, Kyoto University as a transfer student of the Doctor course.