Maternal genetic effects throughout the life of the dam in Pirenaica beef cattle. a random regression model approach.

In beef cattle, dams play a crucial role in shaping the pre- and postnatal environment for the growth of their offspring. Acknowledging the substantial impact of maternal influence on the early development of calves, researchers utilize maternal animal models. These models take into account both maternal genetic and permanent environmental effects, operating under the assumption that these influences remain constant throughout the productive life of the cow. Nevertheless, it cannot be ruled out that these genetic and environmental effects may evolve throughout the lifespan of the cows. Therefore, this study aims to describe the changes in genetic and environmental maternal effects over the productive lifespan of cows. To accomplish this goal, we utilized random regression models, incorporating the age of the dam effect, maternal genetic effects, and environmental permanent effects using Legendre orthogonal polynomials. Additionally, the analytical model incorporated a covariate to adjust for the calf's age at recording, a two-level sex effect, a random herd-year-season effect, and an additive direct genetic effect associated linked to the calf. The dataset comprised information from dams aged between 2 and 16 years, resulting in a final database that comprised weight records of 58 332 calves from 21 673 dams. The average weight at 90 days was 135.0 ± 39.3 kg, and the mean age of the dam at calving was 7.03 ± 3.41 years. We evaluated models incorporating 2, 3, 4, 5, and 6 orthogonal polynomials alongside the standard maternal animal model. Afterward, we selected the model with five orthogonal polynomials based on the Akaike Information Criteria. The Restricted Maximum Likelihood estimates within this model indicated a direct heritability of around 0.50, and a maternal heritability ranging between 0.15 and 0.25, exhibiting a consistent increase between 4, 5 to 13 years. The genetic correlation estimates between direct and maternal genetic effects remained stable at approximately -0.55 across the lifespan of the cows. Furthermore, maternal genetic correlations between different ages of the dam decreased to around 0.7 for more distant age points. The maternal permanent correlations were notably lower, occasionally even reaching negative values, suggesting variability in environmental influence on maternal effects over the productive lifespan of the cow. Finally, the model enables the prediction of breeding values for the maternal genetic effects of the cow across its lifespan, providing opportunities for innovative selection strategies on the maternal side.

EZH2 mutations at diagnosis in follicular lymphoma: a promising biomarker to guide frontline treatment.

EZH2 is mutated in nearly 25% of follicular lymphoma (FL) cases. Little is known about how EZH2 affects patients' response to therapy. In this context, the aim of this study was to retrospectively analyze the frequency of mutations in EZH2 at diagnosis in tissue and ctDNA in patients with FL and to assess the patients' outcomes after receiving immunochemotherapy, depending on the EZH2 mutation status. Among the 154 patients included in the study, 27% had mutated EZH2 (46% with high-grade and 26% with low-grade FL). Of the mutated tissue samples, the mutation in ctDNA was identified in 44% of cases. EZH2 mutation in ctDNA was not identified in any patient unmutated in the tissue.Unmutated patients who received R-CHOP had significantly more relapses than patients who received R-Bendamustine (16/49 vs. 2/23, p = 0.040). Furthermore, our results show that patients with mutated EZH2 treated with R-CHOP vs. those treated with R-Bendamustine present a lower incidence of relapse (10% vs. 42% p = 0.09 at 4 years), a higher PFS (92% vs. 40% p = 0.039 at 4 years), and higher OS (100% vs. 78% p = 0.039 at 4 years). Based on these data, RCHOP could be a more suitable regimen for mutated patients, and R-bendamustine for unmutated patients. These findings could mean the first-time identification of a useful biomarker to guide upfront therapy in FL.

Knowledge, attitudes, and practices regarding dengue, chikungunya, and Zika in Cali, Colombia.

Dengue fever (DENF), chikungunya (CHIK), and Zika are responsible for the majority of the burden caused by vector-borne diseases (VBDs); which are produced by viruses primarily transmitted by the Aedes mosquito. Aedes have become prolific in urban areas due to a combination of climate change, rapid urbanization, increased human mobility, and globalization, causing the three VBDs to emerge in novel regions. Community knowledge can provide detailed insights about the spatial heterogeneity of disease risk and rates within a particular region, improving public health interventions. Knowledge, Attitude, and Practice (KAP) surveys are used to shed light on at-risk communities' understanding of the vector, the pathogen, prevention and treatment strategies. Little is known how KAP varies among diseases, and among neighborhoods within a city. Understanding KAP variation among co-circulating VBDs at a fine-level, especially differences between endemic and emerging diseases, can improve targeted interventions, education programs, and health policy. We administered KAP surveys to 327 individuals in healthcare centers and selected neighborhoods in Cali, Colombia in June 2019. We utilized generalized linear models (GLMs) to identify significant predictors of KAP. Our findings suggest that knowledge is related to community characteristics (e.g. strata), while attitudes and practices are more related to individual-level factors. Access to healthcare also forms significant predictor of residents participating in preventative practices. The results can be leveraged to inform public health officials and communities to motivate at-risk neighborhoods to take an active role in vector surveillance and control, while improving educational and surveillance resources in Cali, Colombia.

Resistance to the proapoptotic effects of interferon-gamma on melanoma cells used in patient-specific dendritic cell immunotherapy is associated with improved overall survival.

The use of whole cell tumor vaccines and various means of loading antigen onto dendritic cells have been under investigation for over a decade. Induction of apoptosis and the exposure of immune-stimulating proteins are thought to be beneficial for the use in immunotherapy protocols, but conclusive evidence in the clinical setting has been lacking. Incubation of melanoma cell lines with interferon-gamma (IFN-γ) increased phosphatidylserine and calreticulin exposure, but not in the IFN-γ-resistant cell line Lu-1205. Short-term autologous melanoma cell lines used for loading dendritic cells for immunotherapy showed differential response to the pro-apoptotic effects of IFN-γ. These IFN-γ-treated tumor cells (TCs) were irradiated and used for loading antigen for dendritic cell therapy. A log-rank comparison of survival for patients whose TCs were found to be either sensitive (upregulated phosphatidylserine and calreticulin) or insensitive to IFN-γ revealed a strongly significant correlation to progression-free (p = 0.003) and overall survival (p = 0.002) favorably in those patients whose cell lines were resistant to the proapoptotic effect of IFN-γ. These results suggest that the use of IFN-γ in anti-melanoma dendritic cell-based immunotherapy may only be beneficial when the cells do not undergo apoptosis in response to IFN-γ and support the contention that the use of some apoptotic cells in vaccines may be detrimental.

Adaptation in a spider mite population after long-term evolution on a single host plant.

Evolution in a single environment is expected to erode genetic variability, thereby precluding adaptation to novel environments. To test this, a large population of spider mites kept on cucumber for approximately 300 generations was used to establish populations on novel host plants (tomato or pepper), and changes in traits associated to adaptation were measured after 15 generations. Using a half-sib design, we investigated whether trait changes were related to genetic variation in the base population. Juvenile survival and fecundity exhibited genetic variation and increased in experimental populations on novel hosts. Conversely, no variation was detected for host choice and developmental time and these traits did not evolve. Longevity remained unchanged on novel hosts despite the presence of genetic variation, suggesting weak selection for this trait. Hence, patterns of evolutionary changes generally matched those of genetic variation, and changes in some traits were not hindered by long-term evolution in a constant environment.

Vertebral osteoma in a dromedary camel.

A case of vertebral osteoma observed in a female 4-year-old dromedary camel is presented. The patient showed a progressive ataxia, incoordination and finally a permanent recumbence position. Treatment was unfruitful and the animal was humanely euthanized. Postmortem examination revealed an expansive growth at vertebral body of the 10th thoracic vertebra, which was histologically classified as an osteoma. To the author's knowledge, this would be the first description of an osteoma in a camelid species.

Psychodrama groups for girls coping with trauma.

This study evaluated the effectiveness of psychodrama groups with traumatized middle-school girls. Comparisons of treatment and control group members' pre- and postintervention adjustment revealed significant decreases in group participants' self-reported difficulties in withdrawn behavior and anxiety/depression. Interviews with the participants reinforced the value of psychodrama group participation in the resolution of trauma and in increasing a sense of competence and self-efficacy. A brief outline of the group structure and a description of the process offer examples that illustrate the practice methodology and provide guidance for conducting psychodrama groups with vulnerable populations. Concerns with safety and containment are addressed.

Methods for reducing the ammonia in hybridoma cell cultures.

The factors which limit the proliferation of eukaryotic cells in vitro are still not well known. Ammonia is believed to be toxic for mammalian cell proliferation and secretion. We have tried two approaches to reducing the ammonia in the medium. We first limited the ammonia produced by the cells by replacing glutamine by glutamate. Then, we used two chemical engineering methods to eliminate accumulated ammonia. In one the used medium was passed through a natural cation exchanger: the clinoptilolite. In the other, the culture medium was passed through a hydrophobic microporous hollow fiber module. Replacing the glutamine by glutamate reduced the medium ammonia concentration. The physicochemical removal of ammonia induced a better cell growth, but not a better specific antibody secretion.