World Primates Research Articles

Fatal Human Alphaherpesvirus 1 Infection in Free-Ranging Black-Tufted Marmosets in Anthropized Environments, Brazil, 2012-2019.

Human alphaherpesvirus 1 (HuAHV1) causes fatal neurologic infections in captive New World primates. To determine risks for interspecies transmission, we examined data for 13 free-ranging, black-tufted marmosets (Callithrix penicillata) that died of HuAHV1 infection and had been in close contact with humans in anthropized areas in Brazil during 2012–2019. We evaluated pathologic changes in the marmosets, localized virus and antigen, and assessed epidemiologic features. The main clinical findings were neurologic signs, necrotizing meningoencephalitis, and ulcerative glossitis; 1 animal had necrotizing hepatitis. Transmission electron microscopy revealed intranuclear herpetic inclusions, and immunostaining revealed HuAHV1 and herpesvirus particles in neurons, glial cells, tongue mucosal epithelium, and hepatocytes. PCR confirmed HuAHV1 infection. These findings illustrate how disruption of the One Health equilibrium in anthropized environments poses risks for interspecies virus transmission with potential spillover not only from animals to humans but also from humans to free-ranging nonhuman primates or other animals.

Immunoreaction to xenogenic tissue in cardiac surgery: alpha-Gal and beyond.

The ability of the immune system to distinguish self from non-self, reacting only to non-self, is essential for immune homeostasis. The mechanisms by which the immune system recognizes and responds to xenogenic tissue heart valves likely involve the initial activation of the innate immune system, with subsequent adaptive immune activation. The antigenicity of xenogeneic tissue constructs, primarily of porcine and bovine origin, has been extensively investigated and several antigenic epitopes have been identified. Some of them have been more exhaustively studied to avoid or at least reduce the immunoreaction triggered by their presence. Galactose-α-1,3-galactose (alpha-Gal) is a carbohydrate epitope present on the cells of all mammals (Fig. 1A). However, in ancestral Old World monkeys and apes, the gene for the enzyme alpha-1,3-galactosyltransferase, essential for the synthesis of alpha-Gal, resulted inactivated [1]. As a consequence, humans and recent Old World primates do not express the epitope. For xenotransplantation, i.e. transplantation of organs from pigs into humans, the mammals' anti-alpha-Gal antibodies represent a major immune barrier [1] (Fig. 1B).

An open access resource for functional brain connectivity from fully awake marmosets

The common marmoset (Callithrix jacchus) is quickly gaining traction as a premier neuroscientific model. However, considerable progress is still needed in understanding the functional and structural organization of the marmoset brain to rival that documented in longstanding preclinical model species, like mice, rats, and Old World primates. To accelerate such progress, we present the Marmoset Functional Brain Connectivity Resource (marmosetbrainconnectome.org), currently consisting of over 70 h of resting-state fMRI (RS-fMRI) data acquired at 500 µm isotropic resolution from 31 fully awake marmosets in a common stereotactic space. Three-dimensional functional connectivity (FC) maps for every cortical and subcortical gray matter voxel are stored online. Users can instantaneously view, manipulate, and download any whole-brain functional connectivity (FC) topology (at the subject- or group-level) along with the raw datasets and preprocessing code. Importantly, researchers can use this resource to test hypotheses about FC directly – with no additional analyses required – yielding whole-brain correlations for any gray matter voxel on demand. We demonstrate the resource's utility for presurgical planning and comparison with tracer-based neuronal connectivity as proof of concept. Complementing existing structural connectivity resources for the marmoset brain, the Marmoset Functional Brain Connectivity Resource affords users the distinct advantage of exploring the connectivity of any voxel in the marmoset brain, not limited to injection sites nor constrained by regional atlases. With the entire raw database (RS-fMRI and structural images) and preprocessing code openly available for download and use, we expect this resource to be broadly valuable to test novel hypotheses about the functional organization of the marmoset brain.

Non-thrombotic pulmonary embolism of brain, liver, or bone marrow tissues associated with traumatic injuries in free-ranging neotropical primates.

From 2016 to 2019, Southeastern Brazil faced an outbreak of yellow fever (YF) affecting both humans and New World primates (NWP). The outbreak was associated with a marked increase in traumatic lesions in NWP in the affected regions. Non-thrombotic pulmonary embolization (NTPE) can be a consequence of massive traumatic events, and it is rarely reported in human and veterinary medicine. Here, we describe NTPE of the brain, liver, and bone marrow in free-ranging NWP, highlighting the epidemiological aspects of these findings and the lesions associated with this condition, including data on traumatic injuries in wild NWP populations during the course of a recent YF outbreak. A total of 1078 NWP were necropsied from January 2017 to July 2019. Gross traumatic injuries were observed in 444 marmosets (44.3%), 10 howler monkeys (23.2%), 9 capuchins (31.0%), 1 titi-monkey (50.0%), and 1 golden lion tamarin (33.3%). NTPE was observed in 10 animals, including 9 marmosets (2.0%) and 1 howler monkey (10.0%). NTPE was identified in the lung and comprised hepatic tissue in 1 case, brain tissue in 1 case, and bone marrow tissue in 8 cases. Although uncommon, it is important to consider NTPE with pulmonary vascular occlusion during the critical care of traumatized NWP. In addition, this study highlights the importance of conservational strategies and environmental education focusing on One Health, not only to protect these free-ranging NWP populations but also to maintain the efficacy of epidemiological surveillance programs.

A Robust Microbead Occlusion Model of Glaucoma for the Common Marmoset.

PurposeTo establish a robust experimental model of glaucoma in the common marmoset (Callithrix jacchus), a New World primate, using an intracameral microbead injection technique.MethodsElevated intraocular pressure (IOP) was induced by an injection of polystyrene microbeads. Morphologic changes in the retina and optic nerve of glaucomatous eyes were assessed and electroretinogram (ERG) recordings were performed to evaluate functional changes.ResultsMicrobead injections induced a sustained IOP elevation for at least 10 weeks in a reproducible manner. At the end of the 10-week experimental period, there was significant loss of retinal ganglion cells (RGCs) in all quadrants and eccentricities, although it was more prominent in the mid-peripheral and peripheral regions. This was consistent with a thinning of the Retinal nerve fiber layer (RNFL) seen in spectral domain optical coherence tomography scans. Surviving RGCs showed marked changes in morphology, including somatic shrinkage and dendritic atrophy. Retinas also showed significant gliosis. The amplitude of the ERG photopic negative response, with subsequent a- and b-wave changes, was reduced in glaucomatous eyes. The optic nerve of glaucomatous eyes showed expanded cupping, disorganization of the astrocytic matrix, axonal loss, and gliosis.ConclusionsWe developed a robust and reproducible model of glaucoma in the marmoset. The model exhibits both structural and functional alterations of retina and optic nerve characteristic of glaucoma in humans and animal models.Translational RelevanceThe glaucoma model in the marmoset described here forms a robust method to study the disease etiology, progression, and potential therapies in a nonhuman primate, allowing for more effective translation of animal data to humans.

Presence and potential distribution of malaria-infected New World primates of Costa Rica

BackgroundIn South and Central America, Plasmodium malariae/Plasmodium brasilianum, Plasmodium vivax, Plasmodium simium, and Plasmodium falciparum has been reported in New World primates (NWP). Specifically in Costa Rica, the presence of monkeys positive to P. malariae/P brasilianum has been identified in both captivity and in the wild. The aim of the present study was to determine the presence of P. brasilianum, P. falciparum, and P. vivax, and the potential distribution of these parasites-infecting NWP from Costa Rica.MethodsThe locations with PCR (Polymerase Chain Reaction) positive results and bioclimatic predictors were used to construct ecological niche models based on a modelling environment that uses the Maxent algorithm, named kuenm, capable to manage diverse settings to better estimate the potential distributions and uncertainty indices of the potential distribution.ResultsPCR analysis for the Plasmodium presence was conducted in 384 samples of four primates (Howler monkey [n = 130], White-face monkey [n = 132], Squirrel monkey [n = 50], and red spider monkey [n = 72]), from across Costa Rica. Three Plasmodium species were detected in all primate species (P. falciparum, P. malariae/P. brasilianum, and P. vivax). Overall, the infection prevalence was 8.9%, but each Plasmodium species ranged 2.1–3.4%. The niche model approach showed that the Pacific and the Atlantic coastal regions of Costa Rica presented suitable climatic conditions for parasite infections. However, the central pacific coast has a more trustable prediction for malaria in primates.ConclusionsThe results indicate that the regions with higher suitability for Plasmodium transmission in NWP coincide with regions where most human cases have been reported. These regions were also previously identified as areas with high suitability for vector species, suggesting that enzootic and epizootic cycles occur.

Colour Preferences in Relation to Diet in Chimpanzees(Pan troglodytes), Gorillas (Gorilla gorilla) and Mandrills (Mandrillus sphinx)

Although trichromatic colour vision has been extensively studied as it grants significant advantages for Old World primates, it is unknown which selective pressures were behind the trait’s evolution. The leading hypothesis would be that colour vision arose as a foraging adaptation because it allowed individuals to spot food more efficiently. To test this, we exposed 3 chimpanzees (Pan troglodytes), 5 gorillas (Gorilla gorilla) and 3 mandrills (Mandrillus sphinx) to colour cardboard plates to assess whether colours related to diet were the most preferred. The experimental setting was divided into two phases. During the first, animals were provided with colour cardboard plates of only 1 colour per data collection session. The order of colour presentation was randomly determined: white, black, yellow, green and red. In phase 2, primates were simultaneously provided with cardboard plates of all colours. Behavioural interactions with plates were measured using a one-zero group focal sampling (10-s sampling intervals and 20-min observation periods). Results showed that when animals were exposed to only 1 colour at a time, they exhibited different colour preferences depending on the species considered. Chimpanzees preferred red and yellow, the colours linked to fruits, while gorillas selected red and white. Mandrills exhibited fewer differences between colour preferences, with red being the most selected. Furthermore, when all colours were simultaneously provided, individuals chose colours related to diet over black and white. Although there were clear individual differences, our results support that trichromatic colour vision is an advantage in detecting and selecting red items. In the wild, it could be important in the detection of reddish fruits and leaves.

Satb1 expression in retinal ganglion cells of marmosets, macaques, and humans.

Recent advances in single-cell RNA sequencing have enabled the molecular distinction of ganglion cell populations in mammalian retinas. Here we used antibodies against the transcription factor special AT-rich binding protein 1 (Satb1, a protein which is expressed by on-off direction-selective ganglion cells in mouse retina) to study Satb1 expression in the retina of marmosets (Callithrix jacchus), macaques (Macaca fascicularis), and humans. In all species, Satb1 was exclusively expressed in retinal ganglion cells. The Satb1 cells made up ∼2% of the ganglion cell population in the central retina of all species, rising to a maximum ∼7% in peripheral marmoset retina. Intracellular injections in marmoset and macaque retinas revealed that most Satb1 expressing ganglion cells are widefield ganglion cells. In marmoset, Satb1 cells have a densely branching dendritic tree and include broad and narrow thorny, recursive bistratified, and parasol cells, all of which show some costratification with the outer or inner cholinergic amacrine cells. The recursive bistratified cells showed the strongest costratification but did not show extensive cofasciculation as reported for on-off direction-selective ganglion cells in rabbit and rodent retinas. In macaque, Satb1 was not expressed in recursive bistratified cells, but in large sparsely branching cells. Our findings further support the idea that the expression of transcription factors in retinal ganglion cells is not conserved across Old World (human and macaque) and New World (marmoset) primates and provides a further step to link a molecular marker with specific cell types.

Lagothrix flavicauda(Primates: Atelidae)

AbstractLagothrix flavicauda (Humboldt, 1812), commonly known as the yellow-tailed woolly monkey, is one of the largest New World primates. Its diet is based on fruits and leaves, and occasionally flowers, buds, epiphyte roots, invertebrates, and some vertebrates. It is endemic to the cloud forests of northern Peru, in Amazonas, San Martín, Huánuco, Junín, La Libertad, and Loreto departments at elevations from 1,000 to 2,800 m. It lives in groups of up to 30 individuals. Lagothrix flavicauda is listed as “Critically Endangered” (CR) by both the International Union for Conservation of Nature (IUCN) and under Peruvian legislation, and on Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).

Epidemiological, clinical and pathological aspects of lethal acanthocephalosis in captive neotropical primates.

Acanthocephalosis is an important cause of death in captive New World primates (NWP). Once established in a colony, it is extremely difficult to treat and control, quickly spreading among NWP with a high mortality rate. This study aimed to characterize the disease associated with infection with acanthocephalans according to its epidemiological, clinical, and anatomopathological aspects in a captive NWP population. From 2010 to 2020, a Brazilian zoo had recurrent deaths of NWP associated to acanthocephalan parasitism. Clinical and pathological profiles of these animals were analyzed considering the host species, sex, age, weight, clinical signs, therapeutic protocols, and pathological findings. A total of 27 deaths associated with acanthocephalosis were recorded, all lethal cases affected tamarins and lion tamarins, corresponding to 67.5% of total deaths during the course of this study. Ten animals died with no previously detected clinical signs, whereas cases with noticeable clinical signs often had apathy and progressive weight loss, resulting in cachexia. Symptomatic NWP were treated with anthelmintic protocols, antibiotics, and support therapy. However, all hospitalized animals died and had grossly detectable adult acanthocephalans in the intestinal lumen that were identified as Prosthenorchis sp., which were associated with transmural and ulcerative enteritis. This report revealed the impact of acanthocephalosis in a naturally infected captive colony of NWP, particularly affecting tamarins (Saguinus spp.) and lion tamarins (Leontopithecus spp.), with failed treatment and control strategies.

Serological prevalence and risk factors of Toxoplasma gondii in Zoo Mammals in Chile

Toxoplasma gondii is a zoonotic cosmopolitan protozoan that causes a high mortality rate among zoo mammals such as New World primates, meerkats, marsupials and Pallas’ cat. It has been recently reported in Chile, mainly among wild populations, but also as the cause of death of a kangaroo and a mara. However, there has not been a T. gondii report at a Zoo population level in Chile in the last 35 years. The aim of the study was to estimate the seroprevalence and risk factors associated with T. gondii infection in mammals housed in a zoo located in the Metropolitan Region of Chile between 2011 and 2018. In this study, we analyzed 350 samples, from 324 animals, belonging to 57 species of carnivores, non-human primates, macropodids, ungulates and rodents to detect the presence of anti-T. gondii antibodies. Additionally, 20 animals were longitudinally sampled to evaluate intra-zoo infection. Using a commercial indirect Enzyme-Linked Immuno Sorbent Assay (ELISA) test, we detected T. gondii antibodies in 72 (22.2 %) samples. The overall seroprevalence estimates were 48.4 % in felines, 22.9 % in non-feline carnivores, 21.1 % in ungulates and 15.0 % in non-human primates. There were no positive samples from rodents or marsupials. Of animals sampled longitudinally, only a culpeo fox (Lycalopex cualpaeus) became seropositive along the study indicating exposition inside the facility. T. gondii seroprevalence differed significantly in taxonomic groups (p = 0.003), felines are statistically different from non-feline carnivores (NFC) (p = 0.040), ungulate (p = 0.027) and non-human primates (NHP) (p = 0.009). Annual prevalence comparison was performed showing no statistical difference (p = 0.941). A multivariable logistic regression was performed to ascertain the effect of taxonomic groups, proximity to water sources, diet, sex and type of housing on seropositivity. Only taxonomic group was statistically significant, indicating that NFC (OR = 0.35; 95 % CI = 0.15 – 0.83; p = 0.017), ungulates (OR = 0.30; 95 % CI = 0.13 – 0.69; p = 0.005), and NHP (OR = 0.25; 95 % CI = 0.09 – 0.72; p = 0.010) have lower risk of positivity to T. gondii compared to felines. Additionally, a black-faced spider monkey (Ateles chamek) and a siamang (Symphalangus syndactylus) were seropositive, being the first description of T. gondii infection in these species worldwide. As seen in previous studies, the widespread presence and exposure of T. gondii in zoo mammals was confirmed, and there may be contact with the agent and transmission within the zoo, which was confirmed by one animal became seropositive over the time. This fact could be a health problem for animals susceptible to fatal toxoplasmosis.

Sapajus apella as a model for the development of novel therapeutic approaches for Parkinson's disease

ABSTRACT Parkinson's disease (PD) is one of the most important research challenges nowadays. In the past five decades, no significant changes in the elucidation of the whole pathophysiology and therapeutic scenario for PD were found, and possible strategies to stop, reverse or cure the disease seem to be on a far horizon. Historically, the most relevant advances in therapeutics for PD were reached using nonhuman primate (NHP) models. They are considered invaluable models for studies on new therapeutic strategies, due to their unquestionable validity to evaluate the efficiency, reliability, and safety for human use. However, NHP species choice may affect research outcomes and must be evaluated with careful consideration of the trade-offs between convenience, costs, scientific relevance, and clinical predictivity. Sapajus apella is a New World monkey species with prominent characteristics as a model for research on the brain and behavior bearing on the human condition, especially regarding the complex features clinically relevant in PD. Among the New World primates, Sapajus apella monkeys more closely resemble humans in several relevant aspects for investigations in PD than other species that are most used for such purposes. This paper discusses the relevance of Sapajus apella monkeys as model to study and develop new therapeutic approaches for PD based on phylogenetic characteristics, telencephalization coefficient, anatomic structures and pathways, genetic features, immune responses, cognitive abilities, and behavioral repertoires.

Attack of an infant by a female in a troop of howler monkeys (<i>Alouatta pigra</i>)


 
 
 Within the New World primate family of Atelidae, infanticidal attacks are most commonly reported in howler monkeys (Alouatta spp., Crockett, 2003; Knopff et al., 2004; Aguiar et al., 2005; Agoramoorthy and Rudran, 2009; Van Belle et al., 2010; Pavé et al., 2012). The howler monkey species that have been observed to exhibit this behaviour are black and gold howler monkeys (Alouatta caraya, Crockett, 2003; Pavé et al., 2012); Colombian red howler monkeys (A. seniculus, Agoramoorthy and Rudran, 1995; Beltrán and Stevenson, 2012); mantled howler monkeys (A. palliata, Crockett, 2003); brown howler monkeys (Martins et al., 2015); and Yucatán black howler monkeys (A. pigra, Crockett, 2003; Van Belle et al., 2010). In these documented attacks there is a lack of detail regarding the involvement of females, as the male is usually identified as the aggressor. These attacks are likely to occur following the immigration of a new male to a troop (Van Belle et al., 2010; Beltrán and Stevenson, 2012), up to five months after taking over a troop (Agoramoorthy and Rudran, 2009). A majority of infanticidal attacks in howler monkeys involve assumed unrelated assailant and victim, therefore these instances align with the sexual selection hypothesis (Hrdy, 1979).
 
 

Architectural properties of the musculoskeletal system in the shoulder of two callitrichid primate species derived from virtual dissection

Callitrichidae are small, arboreal New World primates that utilize a variety of locomotor behaviors including trunk-to-trunk leaping (TTL) and horizontal locomotion which involve differential functional demands. Little is known about the relationship between the preferred locomotor behavior and musculoskeletal architecture of these primates. In this study, we compared the musculoskeletal architecture of selected shoulder muscles in two cadavers each of the trunk-to-trunk leaper Cebuella pygmaea and the mainly pronograde quadrupedally moving Saguinus imperator subgrisescens. Contrast-enhanced microfocus computed tomography (µCT) was used to virtually dissect the cadavers, produce muscle maps, and create 3D reconstructions for an image-based analysis of the muscles. Muscle lengths, muscle volumes, and osteological muscle moment arms were measured, and the anatomical cross-sectional areas (ACSA) were calculated. We expected the muscles of the forelimb of S. imperator to be larger in volume and to be relatively shorter with a larger ACSA due to a higher demand for powerful extension in the forelimbs of this horizontally locomoting species. For C. pygmaea, we expected relatively larger moment arms for the triceps brachii, supraspinatus, infraspinatus and subscapularis, as larger moment arms present an advantage for extensive vertical clinging on the trunk. The muscles of S. imperator were relatively larger in volume than in C. pygmaea and had a relatively larger ACSA. Thus, the shoulder muscles of S. imperator were suited to generate relatively larger forces than those of C. pygmaea. Contrary to our expectations, there were only slight differences between species in regard to muscle lengths and moment arms, which suggests that these properties are not dependent on the preferred locomotor mode. The study of this limited dataset demonstrates that some but not all properties of the musculoskeletal architecture reflect the preferred locomotor behavior in the two species of Callitrichidae examined.

The Kidney-Associated Microbiome of Wild-Caught Artibeus spp. in Grenada, West Indies.

Simple SummaryBats are increasingly being recognized as important integrants of zoonotic disease cycles. Studying bat microbiomes could potentially contribute to the epidemiology of emerging infectious diseases in humans. Furthermore, studying the bat’s microbiome gives us the opportunity to look at the microbiome evolution in mammals. Bat microbiome studies have focused mainly on the gut microbiome, but little is known of the microbiome of the kidney, another potential source of disease transmission. Furthermore, many studies on microbiome found in the literature are based on captive animals, which usually alters the natural microbiome. Here, we analyzed kidney samples of wild-caught Artibeus spp., a fructivorous bat species from Grenada, West Indies, using metagenomics.Bats are capable of asymptomatically carrying a diverse number of microorganisms, including human pathogens, due to their unique immune system. Because of the close contact between bats and humans, there is a possibility for interspecies transmission and consequential disease outbreaks. Herein, high-throughput sequencing was used to determine the kidney-associated microbiome of a bat species abundant in Grenada, West Indies, Artibeus spp. Results indicate that the kidney of these bats can carry potential human pathogens. An endogenous retrovirus, Desmodus rotundus endogenous retrovirus isolate 824, phylogenetically related to betaretroviruses from rodents and New World primates, was also identified.

A Muscle‐fiber Comparison in New World and Old World Monkeys Based on Brain Size, Body Mass and Locomotor Style

This study is part of a larger one (Muchlinski et al., 2018) focusing on the relationship between muscle mass and brain mass in primates. Previous studies have demonstrated a negative correlation between brain size and type I fibers in lemuroideea(N=7) and hominoid primates (N=7), suggesting that as brain mass increases type I muscle-fiber composition decreases. Based on these observations we hypothesized that platyrrhine and cercopithecidae primates would correspondingly have an increase in type II fibers in accordance to their brain mass to account for other more expensive tissue. Our goal was to measure type I and type II fiber distribution in New and Old World primates using immunohistochemistry to develop a muscle fiber distribution profiles and analyze the effect of fiber distribution on endocranial volume (ECV). Two upper-limb (deltoid and pectoralis major) and two hind-limb muscles (gastrocnemius and soleus) were sampled from 7 platyrrhine, 4 cercopithecidae as well as the Philippine tarsier (N=12), representing a range of body size (240-7765g) and locomotory styles. FFPE samples were H&E stained and immunostained using type I and type II myosin heavy-chain antibodies (abcam, 1:750). Pectoralis Major fiber compositions quantified from C. syrichta (3.36cc), A. azazae (20.67cc), C. hamlyni (62.5cc) and S. apella (65.72cc) demonstrate a reduction in Type I fibers; 57.27%, 33.85%, 20.59 and 18.17% respectively as ECV increases, consistent across upper and lower-limb muscles and supporting a negative correlation between brain mass and type I fibers. Predictive modeling using multiple linear regression found muscle mass (g), locomotory style, body mass (g) and % muscle fiber composition to be the greatest explanatory variables in predicting brain size (R²= 0.99 and RMSE = 4.0882). Data from these studies can be used to address evolutionary questions in relation to the evolution of energetics and potential influences from muscle mass, body size and locomotory style.

Molecular Characterization of Blastocystis in Captive and Free-Ranging New World Primates, Platyrrhini.

Blastocystis species are widely distributed micro-eukaryote parasites found in both human and nonhuman primates. Despite having a global distribution, descriptions of Blastocystis subtype diversity in neotropical primates is largely limited to captive animals. The aim of this study was to molecularly characterize the presence of Blastocystis in free-ranging black-headed night monkeys, Aotus nigriceps, and to analyze Blastocystis heterogeneity in primates of the Parvorder Platyrrhini. We analyzed Blastocystis small sub-unit ribosomal DNA (SSUrDNA) from both A. nigriceps and Azara's night monkey, A. azarae boliviensis, in Southeastern Peru. We also included additional Blastocystis sequence from other neotropical primate studies to explore the distribution and host specificity of Blastocystis subtypes (ST) throughout the neotropics. Thirteen percent of A. nigriceps samples were Blastocystis positive. Only ST8 was amplified in A. nigriceps and this partial DNA sequence was highly similar to ST8 sequence previously obtained from a human in Brazil. In our analysis of all available Blastocystis SSU sequences from primates of the Parvorder Platyrrhini, we found 15 monophyletic lineages corresponding to previously described subtypes ST1-ST10, ST12-15, and ST17. Blastocystis SSU sequences amplified from A. nigriceps fecal samples shared high sequence similarity to isolates found in several other neotropical primates, Alouatta palliata, A. caraya, Ateles fusciceps, and Lagothrix. Similar subtypes have been found in human and captive primates which supports the possibility of transmission when in close contact. Expanded sampling of sympatric neotropical primates in the wild will establish whether subtypes and clades are limited to taxonomic group or whether transmission occurs between overlapping species.

Efficiency of whole-exome sequencing in old world and new world primates using human capture reagents.

Whole-exome sequencing (WES) can expedite research on genetic variation in non-human primate (NHP) models of human diseases. However, NHP-specific reagents for exome capture are not available. This study reports the use of human-specific capture reagents in WES for olive baboons, marmosets, and vervet monkeys. Exome capture was carried out using the SureSelect Human All Exon V6 panel from Agilent Technologies, followed by high-throughput sequencing. Capture of protein-coding genes and detection of single nucleotide variants were evaluated. Exome capture and sequencing results showed that more than 97% of old world and 93% of new world monkey protein coding genes were detected. Single nucleotide variants were detected across the genomes and missense variants were found in genes associated with human diseases. A cost-effective approach based on commercial, human-specific reagents can be used to perform WES for the discovery of genetic variants in these NHP species.

Neural network of social interaction observation in marmosets.

A crucial component of social cognition is to observe and understand the social interactions of other individuals. A promising nonhuman primate model for investigating the neural basis of social interaction observation is the common marmoset (Callithrix jacchus), a small New World primate that shares a rich social repertoire with humans. Here, we used functional magnetic resonance imaging acquired at 9.4 T to map the brain areas activated by social interaction observation in awake marmosets. We discovered a network of subcortical and cortical areas, predominately in the anterior lateral frontal and medial frontal cortex, that was specifically activated by social interaction observation. This network resembled that recently identified in Old World macaque monkeys. Our findings suggest that this network is largely conserved between New and Old World primates and support the use of marmosets for studying the neural basis of social cognition.

My Old World chap, this α-gal is not for you

30 million years ago, ancestors of Old World primates lost the ability to produce α-gal. In this issue of Cell Host & Microbe, Singh etal. (2021) show that the loss is associated with increased resistance to sepsis, but that this advantage comes alongside a cost of accelerated reproductive senescence.