Quantification of the impacts of climate warming and crop management on canola phenology in Punjab,Pakistan

Yield is influenced by the length of the growing season, which is affected by weather conditions and management practices of a crop, including sowing dates and shifting of cultivars. It is necessary to understand the effects of agronomic management practices and weather variables on phenological stages and crop phases in order to develop strategies for adaptation of agricultural systems to changes in climatic conditions. The goal of this study was to determine the impact of warming trends on phenology of canola from 1980 to 2014 for central and southern Punjab, Pakistan. Sowing, emergence, anthesis and physiological maturity dates were delayed by an average of 6.02, 3.14, 3.31 and 1.89 days per decade, respectively. The duration of sowing to anthesis, sowing to physiological maturity and anthesis to physiological maturity phases decreased an average 2.71, 4.13 and 1.42 days per decade, respectively, for all 10 locations that were analysed in this study. The sowing, emergence, anthesis and physiological maturity dates were positively correlated with an increase in temperature by an average 2.71, 1.41, 1.49 and 0.85 days per °C, respectively. However, the phenological phases such as sowing to anthesis, anthesis to maturity and sowing to maturity were negatively correlated with an increase in temperature by an average of 1.22, 0.64 and 1.86 days per °C, respectively, for all 10 locations. Applying a process‐based CSM‐CROPGRO‐Canola model using a standard cultivar (field tested) for all locations and years indicated that the simulated phenological stages occurred earlier due to the warming trend compared to the observed phenological stages. One‐quarter of the negative effects of this thermal trend was compensated by growing new cultivars that had higher thermal time requirements. Therefore, new canola genotypes with a higher number of growing degree day requirement and high temperature tolerance should be a priority for evolving new cultivars.     

MRI characteristics of cerebral microbleeds in four dogs

Cerebral microbleeds in people are small foci of hemosiderin-containing macrophages in normal brain parenchyma. They are the remnant of previous hemorrhage and occur with greater frequency in older individuals. Our purpose was to describe the magnetic resonance (MR) appearance of cerebral microbleeds in four dogs. These lesions appeared as round, hypointense foci measuring ≤4 mm on T2*-gradient-recalled echo images. They were less conspicuous or absent on T2-weighting, being iso- or hypointense, and uniformly invisible on T1-weighted images. No contrast enhancement was seen in any of the cerebral microbleeds. Necropsy-derived histopathologic analysis of one brain confirmed these lesions to be chronic cerebrocortical infarcts containing hemosiderin. The MR changes seen in dogs were analogous to what has been described in people and will be helpful in distinguishing cerebral microbleeds from other brain lesions.     

Natural Heterobilharzia americana infection in horses in Texas

The schistosome Heterobilharzia americana infects dogs, raccoons, and other mammals in the southeastern United States. Migration of eggs into the liver results in parasitic granulomas with varying degrees of fibrosis and inflammation. Recently, hepatic parasitic granulomas in horses were shown to be caused by H. americana infection. In the present study, samples of liver from 11 of 12 horses with hepatic granulomas identified at necropsy (n = 11) or surgical biopsy (n = 1) were used for DNA extraction, polymerase chain reaction amplification and sequencing using primers specific for a portion of the H. americana small subunit ribosomal RNA gene. A polymerase chain reaction amplicon of the correct size was produced from the extracted DNA in 8 of the 11 horses. Amplicons from 5 of the 8 positive horses were sequenced and had 100% identity with H. americana. In all but 2 of the 12 horses, Heterobilharzia was not responsible for the primary clinical disease, and the hepatic granulomas were considered an incidental finding.     

Selection of pea genotypes with partial resistance to <Emphasis Type="Italic">Sclerotinia sclerotiorum</Emphasis> across a wide range of temperatures and periods of high relative humidity

Partial resistance to Sclerotinia sclerotiorum based on stem lesion advancement was assessed for nine wild pea genotypes from five geographic origins and two cultivated genotypes, when peas were inoculated and incubated at all combinations of five temperatures (15.6, 18.3, 21.1, 23.9, 29.4°C) and four period(s) of high relative humidity (PHRH; 12, 24, 48, 72 h). PHRH of 12 and 24 h should not be used when screening plants for resistance to S. sclerotiorum regardless of the incubation temperature, since stem lesions are rarely (2.7%) visible at 12 h and there were no significant differences (P ≤ 0.05) in lesion lengths among and within genotypes at all temperatures assessed after 24 h. However, PHRH of 48 and 72 h are recommended for use to assess partial resistance since significant differences in stem lesion length among the genotypes were observed and characterized for these periods. Genotypes with cool (15.6 and 18.3°C) versus warm (23.9 and 29.4°C) temperature partial resistance to S. sclerotiorum were identified, and genotypes PI 240515 and PI 169603 appear to have the best cool and warm temperature partial resistance, respectively, among the genotypes assessed. A temperature of 21.1°C was the optimal temperature favouring lesion advancement for the majority of the genotypes evaluated. PI 169603 demonstrated the best partial resistance to S. sclerotiorum across the widest temperature and PHRH ranges and is recommended to plant breeders as the best single genotype to develop future cultivars with improved partial resistance to S. sclerotiorum based on stem lesion advancement.     

Long-term analysis of feline calicivirus prevalence and viral shedding patterns in naturally infected colonies of domestic cats

Feline calicivirus (FCV) is a highly infectious respiratory pathogen of domestic cats. The prevalence of FCV in the general cat population is high, particularly in multi-cat households, largely because many clinically recovered cats remain persistently infected carriers. In order to assess how FCV circulates in such groups and to assess the contribution that each individual animal makes to the epidemiology of the disease, we have carried out the first detailed analysis of long-term shedding patterns of FCV in individual cats within naturally infected colonies. The prevalence of FCV in each of the groups on individual sampling occasions ranged from 0% to 91%, with averages for the individual colonies ranging from 6% to 75%. Within each of the colonies, one to three distinct strains of FCV were identified. Individual cats showed a spectrum of FCV shedding patterns over the sampling period which broadly grouped into three categories: those that shed virus relatively consistently, those that shed virus intermittently, and those that appeared never to shed virus. This is the first report identifying non-shedder cats that appear resistant to FCV infection over long periods of time, despite being continually exposed to virus. Such resistance appeared to be age related, which may have been immune-mediated, although by analogy with other caliciviruses, factors such as host genetic resistance may play a role. Given that a proportion of the population appears to be resistant to infection, clearly the cohort of cats that consistently shed virus are likely to provide an important mechanism whereby infection can be maintained in small populations.     

The challenge for the next generation of feline calicivirus vaccines

Feline calicivirus (FCV) has been shown to evolve within individual cats and in the environment of colonies. This evolution and the diversity it creates has important clinical implications, not only for the disease in cats, but also for attempts to control disease by vaccination. Generally speaking, existing vaccines appear to be very effective at controlling the majority of clinical disease. However, some concerns remain including a failure to induce sterilising immunity, occasional vaccine breakdowns, and for live vaccines, occasional vaccine-induced disease. Key areas for future vaccine development include monitoring and broadening the cross-reactivity of vaccine immunity to field viruses, especially the recently evolved highly virulent strains, and attempting to reduce/eliminate field virus shedding by vaccinated cats.     

The increase in prolactin-secreting cells in incubating chicken hens can be mimicked by extended treatment of pituitary cells in vitro with vasoactive intestinal polypeptide (VIP)

Incubation of eggs by birds and lactation in mammals are regulated by pituitary prolactin (PRL) and associated with an increase in pituitary PRL-producing cells or lactotrophs. However, the mechanisms controlling this increase in lactotroph numbers are not known. PRL secretion in birds is regulated by vasoactive intestinal polypeptide (VIP). This study was designed to determine whether VIP treatment could modulate lactotroph abundance in culture. Anterior pituitary cells were isolated from laying Japanese White Silkie hens and cultured for 2 or 6 days in the absence or presence of VIP. PRL-secreting cells were identified by reverse hemolytic plaque assay. Treatment with VIP for 6 days substantially increased the abundance of PRL-secreting cells from 47.5% under basal conditions to 70.6% of all pituitary cells following VIP stimulation. However, 2-day VIP treatment had no effect. Furthermore, the extent to which the hens were allowed to accumulate eggs in a clutch prior to isolation of the pituitaries did not affect the lactotroph response to VIP in vitro. These findings indicate that chronic VIP stimulation may be responsible for the increased abundance of lactotrophs found in the pituitary glands of incubating hens.     

The molecular architecture of axonemes revealed by cryoelectron tomography

Eukaryotic flagella and cilia are built on a 9 + 2 array of microtubules plus >250 accessory proteins, forming a biological machine called the axoneme. Here we describe the three-dimensional structure of rapidly frozen axonemes from Chlamydomonas and sea urchin sperm, using cryoelectron tomography and image processing to focus on the motor enzyme dynein. Our images suggest a model for the way dynein generates force to slide microtubules. They also reveal two dynein linkers that may provide "hard-wiring" to coordinate motor enzyme action, both circumferentially and along the axoneme. Periodic densities were also observed inside doublet microtubules; these may contribute to doublet stability.