Green Beans

In this video the author describes the history of green beans in Appalachia, from their role as one of the Native American's "Three Sisters", and their adoption by European settlers, and also looks at how beans have been utilized in literature

Externalizing subtypes and peer rejection: the impact of a close or conflictual teacher-child relationship

Reactively aggressive and hyperactive-impulsive children have been shown to have a higher risk of being rejected by their peers, which can lead to a multitude of negative outcomes, including psychological and behavioral problems. An environmental factor that may impact the relation between these problem behaviors and peer rejection is the teacher-child relationship. Past research examining how teacher-child relationship factors interact with child characteristics in predicting peer outcomes has produced inconsistent results, possibly due to combining hyperactivity-impulsivity and reactive aggression into the same category, when there is evidence that these constructs should be examined independently. It was hypothesized that due to the negative emotionality associated with reactive aggression, teacher-child closeness and teacher-child conflict would moderate the association between reactive aggression and peer rejection, but not the association between hyperactivity-impulsivity and peer rejection. A sample of 106 girls and 81 boys was assessed in the kindergarten year for teacher-reported behavior problems and the level of closeness and conflict present in the teacher-child relationship. Peer rejection data were collected using a sociometric nomination procedure in kindergarten. Results indicated that teacher-child conflict, but not closeness, moderated the relations between both externalizing subtypes and peer rejection. Implications for future research and a consideration of correlates with teacher-child relationship variables were discussed

HIV Treatment as Prevention: Debate and Commentary-Will Early Infection Compromise Treatment-as-Prevention Strategies?

Universal HIV testing and immediate antiretroviral therapy for infected individuals has been proposed as a way of reducing the transmission of HIV and thereby bringing the HIV epidemic under control. It is unclear whether transmission during early HIV infection—before individuals are likely to have been diagnosed with HIV and started on antiretroviral therapy—will compromise the effectiveness of treatment as prevention. This article presents two opposing viewpoints by Powers, Miller, and Cohen, and Williams and Dye, followed by a commentary by Fraser

ADHD symptoms and diet quality in adolescence: examining indirect effects of eating behaviors and the role of peer problems

Emerging literature has suggested that Attention Deficit/Hyperactivity Disorder (ADHD) may be associated with poorer diet quality, though the processes underlying this link are still unclear. The current study sought to examine how ADHD symptoms are related to diet quality by examining both the direct link between ADHD and diet quality in adolescence, as well as indirect associations through two eating behaviors. External eating, defined as eating in response to external cues, and emotional eating, defined as eating in response to negative affect, were examined as potential mediators of the association between ADHD symptoms and diet quality. Furthermore, this study addressed gaps in the literature by considering how peer problems, a salient environmental context in adolescence, may impact the association between ADHD symptoms and emotional eating. The current study used a path analysis to examine the direct effect of ADHD symptoms at age 15 on diet quality at age 16, as well as the indirect effect through external eating and the indirect effect through emotional eating conditional on peer problems. ADHD symptoms, eating behaviors, and peer problems were measured using questionnaires, while diet quality was assessed through a 24-hour dietary recall. Results revealed a significant direct effect of ADHD symptoms on diet quality, as well as a small but significant indirect effect through external eating, such that higher ADHD symptoms were associated with higher external eating and lower diet quality, as hypothesized. Peer problems significantly moderated the association between ADHD symptoms and emotional eating, such that adolescents with higher ADHD symptoms and higher peer problems were at greatest risk for emotional eating. Contrary to hypotheses, emotional eating was positively associated with diet quality. Implications for future research and clinical interventions are discussed

Ectoparasite fauna of rodents collected from two wildlife research centres in Saudi Arabia with discussion on the implications for disease transmission

The majority of human pathogens are zoonotic and rodents play an important role as reservoirs of manyof these infectious agents. In the case of vector-borne pathogens, rodent reservoirs not only act as a sourceof infection for vectors but also serve as hosts for the vectors themselves, supporting their populations.Current data on rodent-ectoparasite relationships is limited in Saudi Arabia, however, this is needed toassess disease risk and the relative importance of different hosts for the maintenance of vector-bornepathogen cycles. In order to provide baseline data for the region that could be used to assess zoonoticdisease risk, we collected and identified 771 ectoparasite specimens (ticks, fleas and mites) from 161rodents at two wildlife research centres in Saudi Arabia and discuss our results in the context of possiblezoonotic disease risk based on the hosts and vectors present.Deanship of Scientific Research at the King Saud University through the research group project number RGP_VPP_020, a University of Pretoria Postdoctoral Fellowship awarded to A. Harrison and by the DST-NRF South African Research Chair of Behavioural Ecology and Physiology awarded to N.C. Bennett.http://www.elsevier.com/locate/actatropica2016-07-31hb201

Designing an intervention to help people with colorectal adenomas reduce their intake of red and processed meat and increase their levels of physical activity: a qualitative study

Background: most cases of colorectal cancer (CRC) arise from adenomatous polyps and malignant potential is greatest in high risk adenomas. There is convincing observational evidence that red and processed meat increase the risk of CRC and that higher levels of physical activity reduce the risk. However, no definitive randomised trial has demonstrated the benefit of behaviour change on reducing polyp recurrence and no consistent advice is currently offered to minimise patient risk. This qualitative study aimed to assess patients' preferences for dietary and physical activity interventions and ensure their appropriate and acceptable delivery to inform a feasibility trial.Methods: patients aged 60-74 included in the National Health Service Bowel Cancer Screening Programme (NHSBCSP) were selected from a patient tracking database. After a positive faecal occult blood test (FOBt), all had been diagnosed with an intermediate or high risk adenoma (I/HRA) at colonoscopy between April 2008 and April 2010. Interested patients and their partners were invited to attend a focus group or interview in July 2010. A topic guide, informed by the objectives of the study, was used. A thematic analysis was conducted in which transcripts were examined to ensure that all occurrences of each theme had been accounted for and compared.Results: two main themes emerged from the focus groups: a) experiences of having polyps and b) changing behaviour. Participants had not associated polyp removal with colorectal cancer and most did not remember being given any information or advice relating to this at the time. Heterogeneity of existing diet and physical activity levels was noted. There was a lack of readiness to change behaviour in many people in the target population.Conclusion: this study has demonstrated the difficulties involved in developing interventions to change dietary and physical activity behaviour in this population. The need to tailor the intervention to individuals, the lack of knowledge about the aetiology of colon cancer and the lack of motivation to change behaviour are critical factors

Multifunctional Adaptive NS1 Mutations Are Selected upon Human Influenza Virus Evolution in the Mouse

The role of the NS1 protein in modulating influenza A virulence and host range was assessed by adapting A/Hong Kong/1/1968 (H3N2) (HK-wt) to increased virulence in the mouse. Sequencing the NS genome segment of mouse-adapted variants revealed 11 mutations in the NS1 gene and 4 in the overlapping NEP gene. Using the HK-wt virus and reverse genetics to incorporate mutant NS gene segments, we demonstrated that all NS1 mutations were adaptive and enhanced virus replication (up to 100 fold) in mouse cells and/or lungs. All but one NS1 mutant was associated with increased virulence measured by survival and weight loss in the mouse. Ten of twelve NS1 mutants significantly enhanced IFN-β antagonism to reduce the level of IFN β production relative to HK-wt in infected mouse lungs at 1 day post infection, where 9 mutants induced viral yields in the lung that were equivalent to or significantly greater than HK-wt (up to 16 fold increase). Eight of 12 NS1 mutants had reduced or lost the ability to bind the 30 kDa cleavage and polyadenylation specificity factor (CPSF30) thus demonstrating a lack of correlation with reduced IFN β production. Mutant NS1 genes resulted in increased viral mRNA transcription (10 of 12 mutants), and protein production (6 of 12 mutants) in mouse cells. Increased transcription activity was demonstrated in the influenza mini-genome assay for 7 of 11 NS1 mutants. Although we have shown gain-of-function properties for all mutant NS genes, the contribution of the NEP mutations to phenotypic changes remains to be assessed. This study demonstrates that NS1 is a multifunctional virulence factor subject to adaptive evolution

Population‐based cohort study of outcomes following cholecystectomy for benign gallbladder diseases

Background The aim was to describe the management of benign gallbladder disease and identify characteristics associated with all‐cause 30‐day readmissions and complications in a prospective population‐based cohort. Methods Data were collected on consecutive patients undergoing cholecystectomy in acute UK and Irish hospitals between 1 March and 1 May 2014. Potential explanatory variables influencing all‐cause 30‐day readmissions and complications were analysed by means of multilevel, multivariable logistic regression modelling using a two‐level hierarchical structure with patients (level 1) nested within hospitals (level 2). Results Data were collected on 8909 patients undergoing cholecystectomy from 167 hospitals. Some 1451 cholecystectomies (16·3 per cent) were performed as an emergency, 4165 (46·8 per cent) as elective operations, and 3293 patients (37·0 per cent) had had at least one previous emergency admission, but had surgery on a delayed basis. The readmission and complication rates at 30 days were 7·1 per cent (633 of 8909) and 10·8 per cent (962 of 8909) respectively. Both readmissions and complications were independently associated with increasing ASA fitness grade, duration of surgery, and increasing numbers of emergency admissions with gallbladder disease before cholecystectomy. No identifiable hospital characteristics were linked to readmissions and complications. Conclusion Readmissions and complications following cholecystectomy are common and associated with patient and disease characteristics

A Novel Small Molecule Inhibitor of Influenza A Viruses that Targets Polymerase Function and Indirectly Induces Interferon

Influenza viruses continue to pose a major public health threat worldwide and options for antiviral therapy are limited by the emergence of drug-resistant virus strains. The antiviral cytokine, interferon (IFN) is an essential mediator of the innate immune response and influenza viruses, like many viruses, have evolved strategies to evade this response, resulting in increased replication and enhanced pathogenicity. A cell-based assay that monitors IFN production was developed and applied in a high-throughput compound screen to identify molecules that restore the IFN response to influenza virus infected cells. We report the identification of compound ASN2, which induces IFN only in the presence of influenza virus infection. ASN2 preferentially inhibits the growth of influenza A viruses, including the 1918 H1N1, 1968 H3N2 and 2009 H1N1 pandemic strains and avian H5N1 virus. In vivo, ASN2 partially protects mice challenged with a lethal dose of influenza A virus. Surprisingly, we found that the antiviral activity of ASN2 is not dependent on IFN production and signaling. Rather, its IFN-inducing property appears to be an indirect effect resulting from ASN2-mediated inhibition of viral polymerase function, and subsequent loss of the expression of the viral IFN antagonist, NS1. Moreover, we identified a single amino acid mutation at position 499 of the influenza virus PB1 protein that confers resistance to ASN2, suggesting that PB1 is the direct target. This two-pronged antiviral mechanism, consisting of direct inhibition of virus replication and simultaneous activation of the host innate immune response, is a unique property not previously described for any single antiviral molecule

Influenza Virus Ribonucleoprotein Complexes Gain Preferential Access to Cellular Export Machinery through Chromatin Targeting

In contrast to most RNA viruses, influenza viruses replicate their genome in the nucleus of infected cells. As a result, newly-synthesized vRNA genomes, in the form of viral ribonucleoprotein complexes (vRNPs), must be exported to the cytoplasm for productive infection. To characterize the composition of vRNP export complexes and their interplay with the nucleus of infected cells, we affinity-purified tagged vRNPs from biochemically fractionated infected nuclei. After treatment of infected cells with leptomycin B, a potent inhibitor of Crm1-mediated export, we isolated vRNP export complexes which, unexpectedly, were tethered to the host-cell chromatin with very high affinity. At late time points of infection, the cellular export receptor Crm1 also accumulated at the same regions of the chromatin as vRNPs, which led to a decrease in the export of other nuclear Crm1 substrates from the nucleus. Interestingly, chromatin targeting of vRNP export complexes brought them into association with Rcc1, the Ran guanine exchange factor responsible for generating RanGTP and driving Crm1-dependent nuclear export. Thus, influenza viruses gain preferential access to newly-generated host cell export machinery by targeting vRNP export complexes at the sites of Ran regeneration