The effect of group size and individual characteristics on between-group encounters in primates

Between-group encounters are common in non-human primates and can vary from affiliative to aggressive. We extracted data from the literature to test five different hypotheses: 1) where there are group size differences between opposing groups, whether the larger group is more likely to win a between-group encounter than the smaller group; 2) whether the likelihood of a group engaging in aggressive between-group encounters increases with group size; and 3-5) whether dominant, older animals, and/or males are more likely to participate aggressively in between-group encounters than subordinate, younger animals and/or females. Our dataset comprised 52 studies on 31 primate species (3 lemur species, 5 New World monkeys, 19 Old World monkeys and 4 apes). We found that the larger group is more likely to win an encounter against a smaller group than vice-versa. We found no significant relationship between group size and propensity to be aggressive during between-group encounters. We found weak/no support for the effect of age, dominance rank and sex on the frequency of aggression displayed towards outgroup animals during between-group encounters. Species- and population-specific differences in between- and within-group competition and in the degree of the unequal distribution of resources across group members may explain why age, dominance rank and sex are not strong predictors of aggression during between-group encounters

Characterization of an endogenous gene expressed in Aedes aegypti using an orally infectious recombinant Sindbis virus

Sindbis virus expression vectors have been used successfully to express and silence genes of interest in vivo in several mosquito species, including Aedes aegypti, Ae. albopictus, Ae. triseriatus,Culex pipiens, Armigeres subalbatus and Anopheles gambiae. Here we describe the expression of an endogenous gene, defensin, in Ae. aegypti using the orally infectious Sindbis virus, MRE/3′2J expression vector. We optimized conditions to infect mosquito larvae per os using C6/36 Ae. albopictus cells infected with the recombinant virus to maximize virus infection and expression of defensin. Infection with the parental Sindbis virus (MRE/3′2J) did not induce defensin expression. Mosquito larvae infected by ingestion of recombinant Sindbis virus-infected C6/36 cells expressed defensin when they emerged as adults. Defensin expression was observed by western analysis or indirect fluorescent assay in all developmental stages of mosquitoes infected with MRE/3′2J virus that contained the defensin insert. The multiplicity of infection of C6/36 cells and the quantity of infected cells consumed by larvae played an important role in defensin expression. Parental viruses, missing the defensin insert, and/or other defective interfering virus may have contributed to these observations

Cytoplasmic chromatin triggers inflammation in senescence and cancer

Chromatin is traditionally viewed as a nuclear entity that regulates gene expression and silencing. However, we recently discovered the presence of cytoplasmic chromatin fragments that pinch off from intact nuclei of primary cells during senescence, a form of terminal cell-cycle arrest associated with pro-inflammatory responses. The functional significance of chromatin in the cytoplasm is unclear. Here we show that cytoplasmic chromatin activates the innate immunity cytosolic DNA-sensing cGAS-STING (cyclic GMP-AMP synthase linked to stimulator of interferon genes) pathway, leading both to short-term inflammation to restrain activated oncogenes and to chronic inflammation that associates with tissue destruction and cancer. The cytoplasmic chromatin-cGAS-STING pathway promotes the senescence-associated secretory phenotype in primary human cells and in mice. Mice deficient in STING show impaired immuno-surveillance of oncogenic RAS and reduced tissue inflammation upon ionizing radiation. Furthermore, this pathway is activated in cancer cells, and correlates with pro-inflammatory gene expression in human cancers. Overall, our findings indicate that genomic DNA serves as a reservoir to initiate a pro-inflammatory pathway in the cytoplasm in senescence and cancer. Targeting the cytoplasmic chromatin-mediated pathway may hold promise in treating inflammation-related disorders

Is the rapid adaptation paradigm too rapid? Implications for face and object processing

The final publication is available at Elsevier via http://dx.doi.org/10.1016/j.neuroimage.2012.03.065. © 2012. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/Rapid adaptation is an adaptation procedure in which adaptors and test stimuli are presented in rapid succession. The current study tested the validity of this method for early ERP components by investigating the specificity of the adaptation effect on the face-sensitive N170 ERP component across multiple test stimuli. Experiments 1 and 2 showed identical response patterns for house and upright face test stimuli using the same adaptor stimuli. The results were also identical to those reported in a previous study using inverted face test stimuli (Nemrodov and Itier, 2011). In Experiment 3 all possible adaptor-test combinations between upright face, house, chair and car stimuli were used and no interaction between adaptor and test category, expected in the case of test-specific adaptation, was found. These results demonstrate that the rapid adaptation paradigm does not produce category-specific adaptation effects around 170-200 ms following test stimulus onset, a necessary condition for the interpretation of adaptation results. These results suggest the rapid categorical adaptation paradigm does not work.103305-1/Canadian Institutes of Health Research89822-1/Canadian Institutes of Health ResearchMOP-89822/Canadian Institutes of Health Researc

The effect of intergroup competition on intragroup affiliation in primates

Researchers from various disciplines have hypothesized a positive correlation between the level of intergroup contest competition (IGCC) and the evolution of behavioural traits, such as cooperation, altruism and friendship, which promote intragroup affiliation. Empirical support for this hypothesis is, however, scarce and mainly available from humans. We tested whether the level of IGCC affects intragroup affiliation (i.e. intragroup grooming exchange) among male and female nonhuman primates. To quantify intragroup affiliation, we used social network measures and a grooming index. Our measure of IGCC combined frequency of intergroup encounters and proportion of aggressive encounters and was calculated separately for males and females. We ran our analyses on 27 wild groups of primates belonging to 15 species (13 Cercopithecinae, one Colobinae and one Cebinae). Our analyses reveal a clear pattern of correlated evolution between grooming network density and interindividual variation in the number of grooming partners on the one hand and the intensity of IGCC on the other in females, but not males. Thus, our results suggest that the exact nature of the relationship between IGCC and intragroup affiliation is sex specific. These results may be explained by the differential costs and benefits males and females experience during aggressive intergroup confrontations and by sex-specific differences in intragroup affiliation

Chloroquine Mediated Modulation of Anopheles gambiae Gene Expression

Plasmodium development in the mosquito is crucial for malaria transmission and depends on the parasite's interaction with a variety of cell types and specific mosquito factors that have both positive and negative effects on infection. Whereas the defensive response of the mosquito contributes to a decrease in parasite numbers during these stages, some components of the blood meal are known to favor infection, potentiating the risk of increased transmission. The presence of the antimalarial drug chloroquine in the mosquito's blood meal has been associated with an increase in Plasmodium infectivity for the mosquito, which is possibly caused by chloroquine interfering with the capacity of the mosquito to defend against the infection.In this study, we report a detailed survey of the Anopheles gambiae genes that are differentially regulated by the presence of chloroquine in the blood meal, using an A. gambiae cDNA microarray. The effect of chloroquine on transcript abundance was evaluated separately for non-infected and Plasmodium berghei-infected mosquitoes. Chloroquine was found to affect the abundance of transcripts that encode proteins involved in a variety of processes, including immunity, apoptosis, cytoskeleton and the response to oxidative stress. This pattern of differential gene expression may explain the weakened mosquito defense response which accounts for the increased infectivity observed in chloroquine-treated mosquitoes.The results of the present study suggest that chloroquine can interfere with several putative mosquito mechanisms of defense against Plasmodium at the level of gene expression and highlight the need for a better understanding of the impacts of antimalarial agents on parasite transmission