scholarly journals Epitranscriptomic profiling of N6-methyladenosine-related RNA methylation in infant rhesus macaques after multiple sevoflurane anesthesia

Author(s):  
Xiao Chen ◽  
Lingling Shi ◽  
Lei Zhang ◽  
Yanyong Cheng ◽  
Zhenyu Xue ◽  
...  
2010 ◽  
Vol 22 (1) ◽  
pp. 35-44 ◽  
Author(s):  
Erin L. Kinnally ◽  
Genesio M. Karere ◽  
Leslie A. Lyons ◽  
Sally P. Mendoza ◽  
William A. Mason ◽  
...  

AbstractA subset of serotonin (5-HT) pathway polymorphisms has been shown to confer risk for psychological dysfunction, particularly in individuals who experience early adversity. Understanding the developmental processes underlying these Gene × Environment interactions will strengthen the search for risk factors for behavioral dysfunction. We investigated the combined influence of two serotonin pathway polymorphisms and species-atypical, and possibly adverse, rearing (nursery rearing [NR]) on two dimensions of behavioral stress response in infant rhesus macaques. We hypothesized that the experience of NR and possession of both “high-risk” genotypes (genotypes that are thought to confer low 5-HT function) would predict the greatest behavioral stress response to maternal/social separation. Using a matched-pair design, the impact of early experience and the serotonin transporter (rh5-HTTLPR) and monoamine oxidase A (rhMAO-A-LPR) promoter polymorphisms on behavioral reactivity of 136 infant rhesus macaques (90–120 days of age) during a 25-hr social separation/relocation procedure was assessed. Each pair included one infant reared with mother in a large, outdoor field enclosure (field rearing) and one infant reared in a nursery (NR). Pairs were matched for putative gene activity of each polymorphism, sex, age, and weight at testing. Behavioral responses in a “human intruder” test were recorded, and activity and emotional reactivity composites were created to detect different aspects of psychological adaptation to stress. Our hypothesis that high-risk groups would be the most reactive to stress was not entirely borne out. Rh5-HTTLPR × rhMAOA-LPR interactions predicted emotional reactivity and tended to predict behavioral activity scores. Carriers of the two “low-risk” alleles exhibited the lowest behavioral activity, as might be predicted, but carriers of both “high-risk” alleles were two of four genotype groups exhibiting the highest observed Emotional Reactivity. Gene × Gene interactions were exacerbated by the experience of nursery rearing, as predicted, however. Finally, we suggest that genetic or environmental factors may mitigate the risk for behavioral dysregulation illustrated in the patterns of behavioral activity and emotional reactivity displayed by infants.


NeuroImage ◽  
2019 ◽  
Vol 184 ◽  
pp. 372-385 ◽  
Author(s):  
Zheng Liu ◽  
Martha Neuringer ◽  
John W. Erdman ◽  
Matthew J. Kuchan ◽  
Lauren Renner ◽  
...  

1998 ◽  
Vol 66 (8) ◽  
pp. 3705-3710 ◽  
Author(s):  
Tessie B. McNeely ◽  
Joan M. Staub ◽  
Cynthia M. Rusk ◽  
Michael J. Blum ◽  
John J. Donnelly

ABSTRACT Streptococcus pneumoniae is responsible for high rates of pneumococcal bacteremia, meningitis, pneumonia, and acute otitis media worldwide. Protection from disease is conferred by antibodies specific for the polysaccharide (Ps) capsule of the bacteria. Of the four types of group 9 pneumococci, types 9N and 9V cause the most disease, and both types are included in the polyvalent pneumococcal vaccine. The type 9V capsule consists of repeating pentasaccharide units linearly arranged, with an average of 1 to 2 mol of O-acetate side chains per mol of repeat units, added in a complex pattern in which not all repeat units are alike. α-GlcA residues may be O-acetylated in the 2 (17%) or 3 (25%) position and β-ManNAc residues may be O-acetylated in the 4 (6%) or 6 (55%) position. Under certain conditions, the O-acetate side chains are subject to oxidation, which results in subsequent de-O-acetylation of a significant number of the repeat units. This de-O-acetylation could adversely affect the efficacy of a vaccine containing the 9V Ps. A study was undertaken to compare the relative contributions of O-acetate and Ps backbone epitopes in the immune response to S. pneumoniae 9V type-specific Ps. In both an infant rhesus monkey model and humans, antibodies against the non-O-acetylated 9V backbone as well as against O-acetylated 9V Ps were detected. Functional (opsonophagocytic) activity was observed in antisera in which the predominant species of antibody recognized de-O-acetylated 9V Ps. We concluded that the O-acetate side groups, while recognized, are not essential to the ability of the 9V Ps to induce functional antibody responses.


2015 ◽  
Vol 49 ◽  
pp. 135-136
Author(s):  
Laura Hewitson ◽  
Bharathi Gadad ◽  
Wenhao Li ◽  
Stephen Grady ◽  
Britni Curtis ◽  
...  

1992 ◽  
Vol 106 (3) ◽  
pp. 254-261 ◽  
Author(s):  
Ned H. Kalin ◽  
Steven E. Shelton ◽  
Charles T. Snowdon

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