Electronic microchip implants were used to identify groups of crab-eating (Macaca fascicularis) and rhesus (Macaca mulatta) macaques. They were implanted in different body sites and monitored for up to fifteen months. One group of rhesus macaques was trained to present the wrist in which the microchip was placed, to enable it to be read easily with the scanner. An improved method of permanently identifying primates will lead to better record keeping and could benefit the animals’ welfare.

Primates are bred in captivity for a number of purposes, from zoo-based captive breeding programmes for conservation to breeding for biomedical research. In each case, breeding animals that are fit for purpose, either as viable candidates for reintroduction or as valid research models, has presented challenges and resulted in steep learning curves. The breeding of animals for biomedical research has become increasingly focused on the production of animals that are less stressed by captive (specifically laboratory) environments. This is because elevated, particularly chronic, stress responses can result in altered physiological, neurological and behavioural states that have the potential to compromise the validity of scientific results. Selective breeding in captivity to, for example, maximise production, select for docile temperament or specific genotypes for biomedical research, is likely to be counter to natural selective pressures for evolutionary fitness. Given that many natural selective pressures active in the wild are absent in captivity, this paper reviews the selective breeding of primates (especially Old World monkeys) in captivity, its potential negative effects, and options that exist for ameliorating these negative effects.

Antigenic variation in malaria was discovered in Plasmodium knowlesi studies involving longitudinal infections of rhesus macaques (M. mulatta). The variant proteins, known as the P. knowlesi Schizont Infected Cell Agglutination (SICA) antigens and the P. falciparum Erythrocyte Membrane Protein 1 (PfEMP1) antigens, expressed by the SICAvar and var multigene families, respectively, have been studied for over 30 years. Expression of the SICA antigens in P. knowlesi requires a splenic component, and specific antibodies are necessary for variant antigen switch events in vivo. Outstanding questions revolve around the role of the spleen and the mechanisms by which the expression of these variant antigen families are regulated. Importantly, the longitudinal dynamics and molecular mechanisms that govern variant antigen expression can be studied with P. knowlesi infection of its mammalian and vector hosts. Synchronous infections can be initiated with established clones and studied at multi-omic levels, with the benefit of computational tools from systems biology that permit the integration of datasets and the design of explanatory, predictive mathematical models. Here we provide an historical account of this topic, while highlighting the potential for maximizing the use of P. knowlesi – macaque model systems and summarizing exciting new progress in this area of research.

Human–wildlife interactions have reached unprecedented levels, and humans are influencing the earth's ecosystems more rapidly and extensively than ever before. This situation is cause for serious concern, especially since disease interactions between wildlife and humans have been recognized as major conservation threats. In this study, long-tailed macaques, Macaca fascicularis, from 2 forest parks located in north-eastern Thailand were investigated to determine the influence of habitat modification by humans on helminth parasite associations in non-human primates. Macaque populations with contact to anthropogenically modified environments were compared with sylvatic groups in nearby natural environments. In order to test for human–non-human primate transmission of parasites, the local human populations were also examined. Humans were infected with a number of potentially pathogenic parasites, including Opisthorchis viverrini and Strongyloides stercoralis. However, eggs of these helminths were not detected in macaque feces. Thus, no direct parasite transfer from humans to non-human primates could be confirmed. However, macaque groups with more frequent contact with human-modified habitats, and a higher portion of human-provided food in their diet, had significantly higher prevalences and intensities of Strongyloides fuelleborni and of an intestinal fluke (probably Haplorchis sp.) than sylvatic groups. Positive correlations were found between the time foraging on the ground and infection with S. fuelleborni, and the amount of human-provided food and intestinal fluke infection. Human alteration of habitat and associated modifications in non-human primate behaviour are likely to play a role in determining the occurrence, prevalence and intensity of zoonotic helminth infection of wild non-human primates.