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Biology subjects

Landry, T.

Publications and source records attributed to Landry, T..

3 recordsLinked to original sources

Metabolic plasticity facilitates a high-latitude life of feast and famine in Arctic char

O_LIHigh northern latitudes experience extreme winters and pronounced environmental variation. Arctic animals possess remarkable and diverse physiological mechanisms to thrive under this variation, but such mechanisms are poorly studied, particularly in the aquatic realm. C_LIO_LIWe combined Arctic field and laboratory experiments to reveal how one of Earths most northerly distributed fish species, the Arctic char, seasonally adjusts its metabolism to conserve energy over winter while not feeding and to capitalize on more optimal growth conditions in summer. C_LIO_LILaboratory reared Arctic char were fed or food deprived at common summer (8{degrees}C) and winter (2{degrees}C) temperatures for >120 days. Oxygen consumption rates were assessed as a proxy for rate of aerobic metabolic energy expenditure. Cooling from 8 to 2{degrees}C reduced resting aerobic energy expenditure by 35%, while food deprivation independently drove a reduction of 46-50%. Combined, resting energy expenditure was 197% higher under simulated summer (fed at 8{degrees}C) than winter conditions (food deprived at 2{degrees}C). C_LIO_LIReductions in resting energy expenditure with food deprivation were driven, at least in part, by marked tissue-specific decreases in organ size and protein synthesis rates in tissues with central roles in growth and digestion. C_LIO_LIWild adult anadromous Arctic char exhibited, seasonal plasticity consistent with our laboratory experiments. Resting energy expenditure at 10{degrees}C was 27% higher after summer feeding than in the spring after winter fasting, while liver and digestive organ masses were also markedly reduced overwinter. C_LIO_LIIn contrast, peak aerobic metabolic performance and relative heart mass were largely maintained during food deprivation indicating a protection of systems that support aerobic metabolic capacity. C_LIO_LIDespite recruiting strategies for substantial energy savings, wild and laboratory reared Arctic char still largely depleted their on-board fat stores with food-deprivation, underscoring that these strategies are essential when food is limited. Given that the Arctic is among the most rapidly changing regions on Earth, temperatures, productivity, and the timing of key seasonal event are all shifting with implications for the efficacy of such strategies for high-latitude animals. C_LI

zoology↗

The paralogues MAGOH and MAGOHB are oncogenic factors in high-grade gliomas and safeguard the splicing of cell division and cell cycle genes

The exon junction complex (EJC) plays key roles throughout the lifespan of RNA and is particularly relevant in the nervous system. We investigated the roles of two EJC members, the paralogs MAGOH and MAGOHB, with respect to brain tumor development. High MAGOH/MAGOHB expression was observed in 14 tumor types; glioblastoma (GBM) showed the greatest difference compared to normal tissue. Increased MAGOH/MAGOHB expression was associated with poor prognosis in glioma patients, while knockdown of MAGOH/MAGOHB affected different cancer phenotypes. Reduced MAGOH/MAGOHB expression in GBM cells caused alterations in the splicing profile, including re-splicing and skipping of multiple exons. The binding profiles of EJC proteins indicated that exons affected by MAGOH/MAGOHB knockdown accumulated fewer complexes on average, providing a possible explanation for their sensitivity to MAGOH/MAGOHB knockdown. Transcripts (genes) showing alterations in the splicing profile are mainly implicated in cell division, cell cycle, splicing, and translation. We propose that high MAGOH/MAGOHB levels are required to safeguard the splicing of genes in high demand in scenarios requiring increased cell proliferation (brain development and GBM growth), ensuring efficient cell division, cell cycle regulation, and gene expression (splicing and translation). Since differentiated neuronal cells do not require increased MAGOH/MAGOHB expression, targeting these paralogs is a potential option for treating GBM.

cancer biology↗

High variation in immune responses and parasite phenotypes in naturally acquired Trypanosoma cruzi infection in a captive non-human primate breeding colony in Texas, USA

Trypanosoma cruzi, the causative agent of human Chagas disease, is endemic to the southern region of the United States where it routinely infects many host species. The indoor/outdoor housing configuration used in many non-human primate research and breeding facilities in the southern U.S. provides the opportunity for infection by T. cruzi and thus provides source material for in-depth investigation of host and parasite dynamics in a natural host species under highly controlled and restricted conditions. For cynomolgus macaques housed at such a facility, we used a combination of serial blood quantitative PCR (qPCR) and hemoculture to confirm infection in >92% of seropositive animals, although each method alone failed to detect infection in >20% of cases. Parasite isolates obtained from 43 of the 64 seropositive macaques were of 2 broad genetic types (discrete typing units, (DTUs) I and IV); both within and between these DTU groupings, isolates displayed a wide variation in growth characteristics and virulence, elicited host immune responses, and susceptibility to drug treatment in a mouse model. Likewise, the macaques displayed a diversity in T cell and antibody response profiles that rarely correlated with parasite DTU type, length of infection, or age of the primate. This study reveals the complexity of infection dynamics, parasite phenotypes, and immune response patterns that can occur in a primate group, despite being housed in a uniform environment at a single location, and the limited time period over which the T. cruzi infections were established. Author SummaryWe evaluated naturally occurring infections of Trypanosoma cruzi, the causative agent of human Chagas disease, in an indoor/outdoor primate colony at a breeding facility in Texas, USA. Using serial quantitative PCR and hemoculture, we confirmed infection in 92% of the 64 seropositive animals, but neither of these two methods confirmed more than 80% of the cases. Parasites by hemoculture fell into two genetic groups (discrete typing units I and IV), and displayed large variation in growth characteristics, elicited cellular and humoral immune responses as well as virulence and drug susceptibility when tested in mice. EKG abnormalities were found in 13 out of 51 qPCR-positive macaques. Our results demonstrate the complexity of these infection parameters in this colony in spite of the uniform and geographically constrained housing conditions of the macaques.

microbiology↗