The components of fruit size in strawberry

High Correlation coefficients have been found in the application of the formula:

$\text{Fresh weight of ripe berry}\text{(g)}\text{=}\text{(Total number of achenes?C)F}\text{(Number of achenes per cm}{}^2\text{of surface}$

to data for a large number of strawberries from nine cultivars. Of the terms in the equation (Total no. of achenes — C) was found to be different in different cultivars and to be related to the position of the berry on the inflorescence, but there was no constant relationship between the achene numbers in the different ranks of berry. Whether the numbers of achenes per berry can be altered by environmental or cultural treatments was not resolved. F, a term having the dimensions of weight per area, represents weight per unit area of berry surface and seems to be constant amongst plants of a cultivar subject to uniform treatment, but differs between cultivars and treatments.The number of achenes per cm² of surface on ripe berries is a measure of berry development in the fruiting season and may be affected by environmental and managerial factors and by internal competition between fruits and leaves on the same plant.The interactions of these factors on berry size enable two stages to be recognised at which size is determined, namely during flower formation, when achene numbers and possibly F are fixed, and during fruit development after pollination when the term for spatial distribution of achenes is settled.It is suggested that an examination of the effects of different treatments on each of the size components might enable a distinction to be drawn between the influence on yield of genetic characteristics on the one hand and intrinsically variable characteristics subject to external influence on the other hand, thus clarifying the type of research and/or development needed to enable growers to achieve maximum yields.     

Respiratory herpesvirus infection in two Indian Ringneck parakeets.

A flock of Indian Ringneck parakeets (Psittacula krameri manillensis) was imported to the United States from Australia. Soon after, 1 parakeet suddenly died, and a second parakeet died after a 2-day course of illness, which consisted of anorexia, lethargy, emaciation, and dyspnea. At necropsy, the affected birds had diffuse consolidation and red discoloration of the lungs, as well as thickened, congested air sacs. The microscopic examination revealed multifocal, necrotizing bronchitis, parabronchitis, and interstitial pneumonia. The lumen of the affected airways contained numerous, large syncytial cells with up to 15 nuclei. The nuclei of these syncytial cells often contained large, eosinophilic inclusion bodies, consistent with herpesvirus. The epithelium of the trachea and air sacs was hypertrophied and contained syncytial cells with intranuclear inclusion bodies similar to the bronchi. In addition, a few intranuclear inclusion bodies were also present in the epithelial cells that line the air capillaries. On ultrastructural examination, the nuclei of degenerating epithelial cells contained clusters of viral nucleocapsid proteins and unenveloped, icosahedral, viral particles that were approximately 90 nm in diameter. In addition, some epithelial cells contained clusters of enveloped viral particles approximately 105 nm in diameter, within the cytocavitary network. These lesions are characteristic of those caused by respiratory herpesvirus of parakeets.     

Comparison of acid–base and electrolyte changes following administration of 6% hydroxyethyl starch 130/0.42 in a saline and a polyionic solution in anaesthetized dogs

Objective

To evaluate the effects of a 6% hydroxyethyl starch (130/0.42) in either a buffered, electrolyte-balanced (HES-BAL) or saline (HES-SAL) carrier solution on electrolyte concentrations and acid–base parameters in healthy anaesthetized dogs.

Evidence of increased Hepatitis E virus exposure in Lao villagers with contact to ruminants

Although pigs are the main reservoir, ruminants have also been shown to be susceptible to hepatitis E virus (HEV). We investigated zoonotic transmission of HEV in rural settings of Lao People's Democratic Republic (Lao PDR) where humans are in close contacts with ruminants and where pigs are rare. Villagers with (n = 171, risk group) and without (n = 155, control group) cattle were recruited in seven villages in Vientiane Capital. Owners of pigs were excluded. Blood, as well as information on socio‐demographics, animal contact, dietary habits and awareness of zoonoses were collected to assess risk factors. Blood and rectal swabs were collected from cattle (n = 173) and other ruminants (27 goat, 5 buffaloes) to measure anti‐HEV antibody and virus prevalence. A similar anti‐HEV antibody seroprevalence was found in cattle (6.8%) and other ruminants (8%). HEV RNA was detected in none of the animal rectal swabs and human sera. Anti‐HEV IgG seroprevalence was higher in cattle farmers than in the control group (59.1% vs. 43.9%, p = 0.008) and increased significantly with age. Other risk factors included male gender, close contact with cattle and consumption of undercooked meat. We find that HEV is highly endemic in rural Laos and provide first evidence that HEV circulates in free‐roaming ruminants with open access to village water sources. Despite some awareness about hygiene, villagers are likely constantly exposed to zoonotic diseases by dietary and lifestyle habits. Cattle farmers had a higher risk of HEV infection than other villagers. Our study highlights the need to raise the awareness of the rural population about water‐ and food‐borne pathogens, and about the role of cattle as a possible source of infection. The knowledge gained on local risk factors and husbandry conditions should guide future awareness raising campaigns and promote appropriate hygienic measures including handwashing and the consumption of safe food and water.     

Host range, distribution, and natural enemies of Bemisia tabaci ‘B biotype’ (Hemiptera: Aleyrodidae) in Turkey

The whitefly Bemisia tabaci (Gennadius) has caused notable damage to vegetable and cotton crops in the eastern Mediterranean region since about 1994, and has become particularly problematic in southern Turkey beginning in 2000. The development of squash silverleaf symptoms in Cucurbita species and the unprecedented high population levels in the region suggested that the B biotype, notable for the latter phenotypes, had been introduced. To test this hypothesis and determine the host distribution of the suspect introduced B biotype and its associated natural enemies, B. tabaci immature instars and adults, and the associated natural enemies were collected from cultivated and uncultivated plant species. From the southern Turkey collections, B. tabaci was found to colonize 152 species from 43 plant families. Of the plant species upon which B. tabaci was found to reproduce, 152 of them were reported as hosts of B. tabaci in Turkey. Five species of predators and two species of parasitoids were identified as natural enemies of the B biotype of B. tabaci in southern Turkey. Using the mitochondrial cytochrome oxidase I gene all B. tabaci were identified as the B biotype of the B. tabaci complex, at 96–100% shared identity with reference B biotype sequences. Results indicate that this invasive biotype has displaced the local Turkey-cotton haplotype that was known to occur previously in southern Turkey.     

Infectivity of pestivirus following persistence of acute infection

Bovine viral diarrhoea virus (BVDV) is an endemic pathogen worldwide and eradication strategies focus on the identification and removal of persistently infected (PI) animals arising after in utero infection. Despite this, acute infections with BVDV can persist for months or years after the removal of the PI source despite repeated screening for PIs and tight biosecurity measures. Recent evidence for a prolonged duration of viraemia in the testicles of bulls following acute BVDV infection suggests the possibility of a form of chronic persistence that may more closely resemble the persistence strategies of hepatitis C virus (HCV). To investigate the potential for virus transmission from infected and recovered cattle to virus naïve hosts we established an acute infection of 5 BVDV-naïve calves and monitored animals over 129 days. Infectious BVDV was detected in white blood cells between days 3 and 7 post-challenge. The animals seroconverted by day 21 post-infection and subsequently were apparently immune and free from infectious virus and viral antigen.Animals were further monitored and purified white blood cells were stimulated in vitro with phytohaemagglutinin A (PHA) during which time BVDV RNA was detected intermittently.Ninety-eight days following challenge, blood was transferred from these apparently virus-free and actively immune animals to a further group of 5 BVDV-naïve calves and transmission of infection was achieved. This indicates that BVDV-infected, recovered and immune animals have the potential to remain infectious for BVDV-naïve cohorts for longer than previously demonstrated.     

Searching for proteins of Mycobacterium avium subspecies paratuberculosis with diagnostic potential by comparative qualitative proteomic analysis of mycobacterial tuberculins

Accurate immunodiagnosis of bovine paratuberculosis is among others hampered by the lack of specific antigens. One of the most frequently used antigen preparations is purified protein derivative (PPD), also known as tuberculin. This crude extract has limitations when used in diagnostic assays due to the presence of cross-reactive antigens. The aim of the current study was to systematically analyze the qualitative protein composition of PPD of the major mycobacterial pathogens.One-dimensional gel electrophoresis followed by tandem mass spectrometry analysis of PPD from Mycobacterium avium subspecies paratuberculosis (MAP), Mycobacterium avium subspecies avium (MAA) and Mycobacterium bovis (MB) identified 156, 95 and 132 proteins, respectively. Comparative sequence analysis led to the selection of a MAP-specific protein (MAP1718c), and finally heterologous expression in Escherichia coli of this and other diagnostic candidate proteins (MAP3515c and MAP1138c (LprG)) enabled evaluation of their immunogenicity. Lymphocyte proliferation responses did not indicate substantial diagnostic potential of the antigens tested. In contrast serum antibody levels for MAP1138c in paratuberculosis infected cows (N = 20) were significantly higher (p < 0.01) than in control animals (N = 20), despite the conserved nature of this protein.In conclusion, this study showed that a combination of proteomics and genomics, starting from complex protein mixtures, present in tuberculins, can reveal novel proteins aiding the development of immunodiagnostics for mycobacterial diseases.