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Global Gene Expression Analysis Identifies Age-Related Differences in Knee Joint Transcriptome during the Development of Post-Traumatic Osteoarthritis in Mice.
Aging and injury are two major risk factors for osteoarthritis (OA). Yet, very little is known about how aging and injury interact and contribute to OA pathogenesis. In the present study, we examined age- and injury-related molecular changes in mouse knee joints that could contribute to OA. Using RNA-seq, first we profiled the knee joint transcriptome of 10-week-old, 62-week-old, and 95-week-old mice and found that the expression of several inflammatory-response related genes increased as a result of aging, whereas the expression of several genes involved in cartilage metabolism decreased with age. To determine how aging impacts post-traumatic arthritis (PTOA) development, the right knee joints of 10-week-old and 62-week-old mice were injured using a non-invasive tibial compression injury model and injury-induced structural and molecular changes were assessed. At six-week post-injury, 62-week-old mice displayed significantly more cartilage degeneration and osteophyte formation compared with young mice. Although both age groups elicited similar transcriptional responses to injury, 62-week-old mice had higher activation of inflammatory cytokines than 10-week-old mice, whereas cartilage/bone metabolism genes had higher expression in 10-week-old mice, suggesting that the differential expression of these genes might contribute to the differences in PTOA severity observed between these age groups
Genome Sequences of Three Vaccine Strains and Two Wild-Type Canine Distemper Virus Strains from a Recent Disease Outbreak in South Africa
Genome Sequences of Three Vaccine Strains and Two Wild-Type Canine Distemper Virus Strains from a Recent Disease Outbreak in South Africa
Canine distemper virus causes global multihost infectious disease. This
report details complete genome sequences of three vaccine and two new wild-type
strains. The wild-type strains belong to the South African lineage, and all three vaccine
strains to the America 1 lineage. This constitutes the first genomic sequences of
this virus from South Africa.The National Zoological Gardens of South Africa and
funded by the National Research Foundation (NRF) Professional Development Program.http://genomea.asm.orgam2018Veterinary Tropical Disease
Phylogenetic analysis of canine distemper virus in South African wildlife
<div><p>Canine distemper virus (CDV) causes a severe contagious disease in a broad range of hosts. This is the first study to genetically characterise CDV strains from four different wildlife species in South Africa. The phylogenetic diversity of CDV is examined, using the haemagglutinin gene. The South African wildlife CDV isolates showed a high degree of similarity to CDV in South African domestic dogs. Phylogenetic analyses confirmed the presence of 12 geographical lineages with CDV strains from South African wildlife falling within the Southern African lineage. The study reveals two possible co-circulating sub-genotypes corresponding to the northern and southern regions of South Africa respectively. CDV strains from the non-canid species were distinct, but similar to CDV isolates from domestic dog and wild canids. Residues at amino acid sites of the SLAM binding region support the notion that CDV strains encoding 519I / 549H are better adapted to non-canid species than canid species. The amino acids present at site 530 are conserved regardless of host species. Strains from South African wild carnivores showed no difference between host species with all strains presenting 530N. All non-canid strains in this study presented the combination 519I/549H. No evidence of host adaptation or lineage grouping was observed for the Nectin-4 binding region. Further studies should include CDV strains isolated from various hosts from a wider geographical range in South Africa.</p></div
Interobserver and intraobserver variability in pH-impedance analysis between 10 experts and automated analysis.
Predicting sepsis-related mortality and ICU admissions from telephone triage information of patients presenting to out-of-hours GP cooperatives with acute infections:A cohort study of linked routine care databases
BackgroundGeneral practitioners (GPs) often assess patients with acute infections. It is challenging for GPs to recognize patients needing immediate hospital referral for sepsis while avoiding unnecessary referrals. This study aimed to predict adverse sepsis-related outcomes from telephone triage information of patients presenting to out-of-hours GP cooperatives.MethodsA retrospective cohort study using linked routine care databases from out-of-hours GP cooperatives, general practices, hospitals and mortality registration. We included adult patients with complaints possibly related to an acute infection, who were assessed (clinic consultation or home visit) by a GP from a GP cooperative between 2017–2019. We used telephone triage information to derive a risk prediction model for sepsis-related adverse outcome (infection-related ICU admission within seven days or infection-related death within 30 days) using logistic regression, random forest, and neural network machine learning techniques. Data from 2017 and 2018 were used for derivation and from 2019 for validation.ResultsWe included 155,486 patients (median age of 51 years; 59% females) in the analyses. The strongest predictors for sepsis-related adverse outcome were age, type of contact (home visit or clinic consultation), patients considered ABCD unstable during triage, and the entry complaints”general malaise”, “shortness of breath” and “fever”. The multivariable logistic regression model resulted in a C-statistic of 0.89 (95% CI 0.88–0.90) with good calibration. Machine learning models performed similarly to the logistic regression model. A “sepsis alert” based on a predicted probability >1% resulted in a sensitivity of 82% and a positive predictive value of 4.5%. However, most events occurred in patients receiving home visits, and model performance was substantially worse in this subgroup (C-statistic 0.70).ConclusionSeveral patient characteristics identified during telephone triage of patients presenting to out-of-hours GP cooperatives were associated with sepsis-related adverse outcomes. Still, on a patient level, predictions were not sufficiently accurate for clinical purposes
SWAPDT : a method for short-time withering assessment of probability for drought tolerance in Camellia sinensis validated by targeted metabolomics
Climate change is causing droughts affecting crop production on a global scale. Classical
breeding and selection strategies for drought-tolerant cultivars will help prevent crop losses.
Plant breeders, for all crops, need a simple and reliable method to identify drought-tolerant
cultivars, but such a method is missing. Plant metabolism is often disrupted by abiotic stress
conditions. To survive drought, plants reconfigure their metabolic pathways. Studies have
documented the importance of metabolic regulation, i.e. osmolyte accumulation such as
polyols and sugars (mannitol, sorbitol); amino acids (proline) during drought. This study
identified and quantified metabolites in drought tolerant and drought susceptible Camellia
sinensis cultivars under wet and drought stress conditions. For analyses, GC-MS and LC-MS
were employed for metabolomics analysis. %RWC results show how the two drought tolerant
and two drought susceptible cultivars differed significantly (p ≤ 0.05) from one another; the
drought susceptible exhibited rapid water loss compared to the drought tolerant. There was a
significant variation (p < 0.05) in metabolite content (amino acid, sugars) between drought
tolerant and drought susceptible tea cultivars after short-time withering conditions. These
metabolite changes were similar to those seen in other plant species under drought conditions,
thus validating this method. The Short-time Withering Assessment of Probability for Drought
Tolerance (SWAPDT) method presented here provides an easy method to identify drought
tolerant tea cultivars that will mitigate the effects of drought due to climate change on crop
losses.The financial support to conduct this research, and study grants for
CN and RK from James Finlay (Kenya) Ltd, George Williamson (Kenya) Ltd, Sotik Tea Company (Kenya) Ltd, Mcleod Russell (Uganda) Ltd, and the Tea Research Institute of Kenya. The C. sinensis cultivars used in this study were provided by the Tea Research Foundation of Central Africa (Malawi) and the Tea Research Institute of Kenya.
Supplementary funding was provided by, the Technology and Human Resources for Industry Programme (THRIP), an initiative of the Department of Trade and Industries of South Africa (dti), the National Research Foundation (NRF) of South Africa, and the University of Pretoria
(South Africa).http://www.elsevier.com/locate/jplph2017-07-31hb2016BiochemistryStatistic
Endoscopy services in KwaZulu-Natal Province, South Africa, are insufficient for the burden of disease: Is patient care compromised?
Background. Endoscopy services are central to the diagnosis and management of many gastrointestinal (GI) diseases.Objective. To evaluate the adequacy of endoscopy services in the public sector hospitals of KwaZulu-Natal (KZN) Province, South Africa, in 2016.Methods. A cross-sectional study was performed using a questionnaire completed by the clinical heads of endoscopy units in the public hospitals in KZN.Results. The heads of 11 of the 12 endoscopy units responded. Two units were in tertiary-level hospitals and nine in regional hospitals. A total of 22 353 endoscopic procedures were performed annually, averaging 2 032 cases per annum per centre; they were performed by 89Â endoscopists, of whom 72 (80.1%) were general surgeons. There were 0.06 registered gastroenterologists (GEs) per 100 000 population. Each endoscopist performed an average of 263 endoscopies per annum. There were 1.18 endoscopy rooms available per unit, and two units had on-site fluoroscopy available. The average waiting period for an upper endoscopy was 27 (range 7 - 60) days, for colonoscopy 29 (range 7 - 90) days and for duodenoscopy/endoscopic retrograde cholangiopancreatography 13 (range 4 - 20) days. This included patients with alarm symptoms for GI cancers. Equipment breakages interrupted most services, except for one hospital that had a service contract. Unit heads cited lack of equipment, trained staff and maintenance contracts as major shortcomings.Conclusions. Endoscopy units in KZN are not adequately equipped to deal with the endoscopy workload and services are plagued by frequent disruptions, which impact negatively on service delivery. There is a need to train more GEs. Patient care is compromised in these public hospitals.
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