Azospirillum brasilense Cd was grown in ammonium–malate mineral salts medium in batch culture and in chemostat continuous culture. It was found that poly-β-hydroxybutyrate synthesis was favored under oxygen limitation in chemostat culture and under high C/N ratios towards the end of exponential growth in batch culture. The degradation and synthesis of poly-β-hydroxybutyrate under starvation conditions occurred in a biphasic pattern and was affected by the poly-β-hydroxybutyrate content of the cells. During a 7-day incubation period in phosphate buffer, the survival and respiration rate of bacteria containing about 40% poly-β-hydroxybutyrate (dry weight) were higher than those of cells containing about 5% poly-β-hydroxybutyrate. Polymer-rich cells fixed atmospheric nitrogen in the absence of exogenous carbon and combined nitrogen. Biphasic nitrogenase activity was observed during starvation. When nitrogenase activity was high, hydroxybutyrate dehydrogenase activity was low and vice versa. Aerotactic response was higher in polymer-rich cells. In the presence of stress factors such as ultraviolet irradiation, dessication, and osmotic pressure poly-β-hydroxybutyrate-poor cells died more rapidly than poly-β-hydroxybutyrate-rich cells.

Tilapia lake virus disease (TiLVD) has emerged to be an important viral disease of farmed Nile tilapia (Oreochromis niloticus) having the potential to impede expansion of aquaculture production. There is a need for rapid diagnostic tools to identify infected fish to limit the spread in individual farms. We report the first detection of TiLV infection by PCR in farmed and wild Nile tilapia from Lake Victoria. There was no difference in prevalence between farmed and wild fish samples (p = .65), and of the 442 samples examined from 191 fish, 28 were positive for TiLV by PCR. In terms of tissue distribution, the head kidney (7.69%, N = 65) and spleen (10.99%, N = 191), samples had the highest prevalence (p < .0028) followed by heart samples (3.45%, N = 29). Conversely, the prevalence was low in the liver (0.71%, N = 140) and absent in brain samples (0.0%, N = 17), which have previously been shown to be target organs during acute infections. Phylogenetic analysis showed homology between our sequences and those from recent outbreaks in Israel and Thailand. Given that these findings were based on nucleic acid detection by PCR, future studies should seek to isolate the virus from fish in Lake Victoria and show its ability to cause disease and virulence in susceptible fish.

No abstract

With the rapid global spread of West Nile virus (WNV) and the endemic state it has acquired in new geographical areas, we hereby bring a thorough serological investigation of WNV in horses in a longstanding endemic region, such as Israel. This study evaluates the environmental and demographic risk factors for WNV infection in horses and suggests possible factors associated with the transition from endemic to epidemic state. West Nile virus seroprevalence in horses in Israel was determined throughout a period of more than a decade, before (1997) and after (2002 and 2013) the massive West Nile fever outbreak in humans and horses in 2000. An increase in seroprevalence was observed, from 39% (113/290) in 1997 to 66.1% (547/827) in 2002 and 85.5% (153/179) in 2013, with persistent significantly higher seroprevalence in horses situated along the Great Rift Valley (GRV) area, the major birds' migration route in Israel. Demographic risk factors included age and breed of the horse. Significantly lower spring precipitation was observed during years with increased human incidence rate that occurred between 1997–2007. Hence, we suggest referring to Israel as two WNV distinct epidemiological regions; an endemic region along the birds' migration route (GRV) and the rest of the country which perhaps suffers from cyclic epidemics. In addition, weather conditions, such as periods of spring drought, might be associated with the transition from endemic state to epidemic state of WNV.

No abstract