Artificial light at night decreases the pupillary light response of dark-adapted toads to bright light

Artificial light at night (ALAN) is expanding worldwide. Many physiological effects have been reported in animals, but we still know little about the consequences for the visual system. The pupil contributes to control incoming light onto the retina. Sudden increases in light intensity evokes the pupil light reflex (PLR). Intrinsically photosensitive retinal ganglion cells (ipRGC) affect PLR and melatonin expression, which largely regulate circadian rhythms and PLR itself. IpRCG receive inputs from various photoreptors with different peak sensitivities implying that PLR could be altered by a broad range of light sources. We predicted ALAN to enhance PLR. Contrary to our prediction, dark-adapted cane toads Rhinella marina, exposed to ALAN (5 lx) for 12 days, exhibited a lower PLR than controls and individuals exposed to 0.04 lx, even after 1 h in bright light. We cannot conclude whether ALAN induced a larger pupil size in dark-adapted toads or a slower initial contraction. Nevertheless, the response was triggered by a light source with an emission peak (590 nm) well above the sensitivity peak of melanopsin, the main photoreceptor involved in PLR. Therefore, ALAN alters the capacity of toads to regulate the incoming light in the eye at night, which may reduce the performance of visually guided behaviors, and increase mortality by predators or road kills at night. This first study emphasizes the need to focus on the effect of ALAN on the vision of nocturnal organisms to better understand how this sensory system is altered and anticipate the consequences for organisms.     

Estimation of genetic parameters in a recurrent selection program in Apple

Combining ability was estimated for 8 tree and 11 agronomic traits in a multi-location apple genetics population to select individuals for the next cycle of selections. Families more than three standard errors away from the general mean were identified for each trait and extreme individuals (with regard to that trait) from those families were selected. On the whole, 148 individuals were chosen based upon individual traits and, in a few cases a combination of traits, in a way that maintains the original diversity within the population. Narrow-sense heritability estimated separately for each site for fruit ribbing, fruit russet, fruit overcolour amount and fruit weight ranged from 0.0–0.13, 0.05–0.58, 0.34–0.40 and 0.27–0.90 respectively. Phenotypic correlation and additive genetic correlation were small and from small to moderately high respectively, between pairs of traits. The implication of these genetic parameter estimates in apple breeding is discussed. This revised version was published online in July 2006 with corrections to the Cover Date.     

Enzyme immunoassay for tenuazonic acid in apple and tomato products

The Alternaria mycotoxin tenuazonic acid was derivatized with succinic anhydride and conjugated to keyhole limpet hemocyanin (KLH) and to horseradish peroxidase (HRP), respectively. The KLH conjugate was used to produce polyclonal antibodies in rabbits. A competitive direct enzyme immunoassay (EIA) for tenuazonic acid was established, which was moderately sensitive for tenuazonic acid [50% inhibition concentration (IC(50)): 320 ± 130 ng/mL] but strongly reacted with tenuazonic acid acetate (IC(50): 23.3 ± 7.5 ng/mL). Therefore, an optimized EIA protocol was established, which employed acetylation of standard and sample extract solutions. The mean standard curve detection limit (IC(30)) for tenuazonic acid acetate was 5.4 ± 2.0 ng/mL, enabling detection limits for tenuazonic acid in apple and tomato products of 25-50 ng/g (150 ng/g in tomato paste). Recoveries in a concentration range of 50-2000 ng/g were 60-130% in apple juice and tomato juice and 40-150% in other tomato products. Tenuazonic acid was detected in apple juice and tomato products from German retail shops at levels of 50-200 ng/g. In conclusion, this novel EIA for tenuazonic acid could be useful within a screening program for Alternaria mycotoxins in food.     

Malassezia dermatitis in dogs in Brazil: diagnosis,evaluation of clinical signs and molecular identification

Skin carriage and quantification of Malassezia yeasts were evaluated in 180 healthy dogs (group 1) and 117 dogs with clinical signs (pruritus, erythema, lichenification/seborrhoea, excoriations and alopecia) that could be related to Malassezia dermatitis (group 2) in Brazil. The lesions in the group 2 dogs were evaluated using CADESI‐03 scores. Samples were collected from five different anatomical areas. Direct examination was performed using the tape strip technique, and results were expressed as the mean number of yeasts per ×1000 microscopic field per dog. For mycological culture, a single piece of sterilized carpet was applied to the same areas sampled for cytology, and transferred onto Dixon’s modified medium. Yeast populations were expressed as mean colony forming units (CFU)/plate. Malassezia isolates were characterized by polymerase chain reaction–restriction endonuclease analysis of the large subunit (LSU) of ribosomal RNA gene. The probability of culturing Malassezia from dogs with skin lesions was significantly higher (P < 0.001) than from healthy dogs. There was a linear trend between CADESI‐03 score and mean CFU/plate. Group 2 dogs with positive cultures had higher CADESI‐03 scores than those with negative cultures (P < 0.05). Almost all isolates were identified as Malassezia pachydermatis. Only one isolate (group 2) was identified as Malassezia furfur. These data suggest that dogs with skin disorders harbouring Malassezia yeasts in quantities higher than 120 mean CFU/plate should be considered as having Malassezia dermatitis. The presence of Malassezia appears to exacerbate clinical lesions in dogs.     

The Role of Weather in Meningitis Outbreaks in Navrongo, Ghana: A Generalized Additive Modeling Approach

Bacterial (meningococcal) meningitis is a devastating infectious disease with outbreaks occurring annually during the dry season in locations within the ??Meningitis Belt??, a region in sub-Saharan Africa stretching from Ethiopia to Senegal. Meningococcal meningitis occurs from December to May in the Sahel with large epidemics every 5?C10?years and attack rates of up to 1000 infections per 100,000 people. High temperatures coupled with low humidity may favor the conversion of carriage to disease as the meningococcal bacteria in the nose and throat are better able to cross the mucosal membranes into the blood stream. Similarly, respiratory diseases such as influenza and pneumonia might weaken the immune defenses and add to the mucosa damage. Although the transmission dynamics are poorly understood, outbreaks regularly end with the onset of the rainy season and may begin anew with the following dry season. In this paper, we employ a generalized additive modeling approach to assess the association between number of reported meningitis cases and a set of weather variables (relative humidity, rain, wind, sunshine, maximum and minimum temperature). The association is adjusted for air quality (dust, carbon monoxide), as well as varying degrees of unobserved time-varying confounding processes that co-vary with both the disease incidence and weather. We present the analysis of monthly reported meningitis counts in Navrongo, Ghana, from 1998?C2008.     

The effects of cyclooxygenase‐2 inhibition on apoptosis and cell cycle distribution using two in vitro models of nasal squamous cell carcinoma

Objective: Despite numerous attempts using a variety of therapeutic modalities, response rates and survival times for canine nasal squamous cell carcinoma remain poor. The goals of this study are to determine if a COX‐2 selective inhibitor induces apoptosis and alters cell cycle distribution in two in vitro models of nasal squamous cell carcinoma, and to establish a basis for future clinical trials using COX‐2 inhibitors as radiosensitizing agents. Methods: The nasal squamous cell carcinoma cell lines FAT‐7 (rat) and RPMI 2650 (human) were purchased from ATCC (Manassas, VA). Cell pellets were stained for COX‐2 expression using standard immunohistochemical techniques. Following the determination of growth kinetics for each cell line, cells were plated in triplicate using 25 cm² tissue culture flasks and incubated with different concentrations of a COX‐2 selective inhibitor (0, 1, 10, 50 and 100 μM) for 72 hours. Cells were stained with Annexin‐V and propidium iodide (Oncogene Research Products) and analyzed with flow cytometry to assess cell viability. Cell cycle distribution was determined using a propidium iodide methodology and flow cytometric analysis. Results: Preliminary results show that the addition of a COX‐2 selective inhibitor caused a dose‐dependent cytotoxicity on the FAT‐7 cells. Viability at 72 hours ranged from 95.4% for control samples to 7.46% for cells incubated at 100 μM. Changes in cell cycle distribution were also detected. Conclusions: Future study is warranted to determine if the addition of a COX‐2 selective inhibitor will increase response rates and overall survival in a population of spontaneously arising canine nasal squamous cell carcinomas.