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Most of our understanding of the ecology and evolution of avian influenza A virus (AIV) in wild birds is derived from studies conducted in the northern hemisphere on waterfowl, with a substantial bias towards dabbling ducks. However, relevant environmental conditions and patterns of avian migration and reproduction are substantially different in the southern hemisphere. Through the sequencing and analysis of 333 unique AIV genomes collected from wild birds collected over 15 years we show that Australia is a global sink for AIV diversity and not integrally linked with the Eurasian gene pool. Rather, AIV are infrequently introduced to Australia, followed by decades of isolated circulation and eventual extinction. The number of co-circulating viral lineages varies per subtype. AIV haemagglutinin (HA) subtypes that are rarely identified at duck-centric study sites (H8-12) had more detected introductions and contemporary co-circulating lineages in Australia. Combined with a lack of duck migration beyond the Australian-Papuan region, these findings suggest introductions by long-distance migratory shorebirds. In addition, on the available data we found no evidence of directional or consistent patterns in virus movement across the Australian continent. This feature corresponds to patterns of bird movement, whereby waterfowl have nomadic and erratic rainfall-dependant distributions rather than consistent intra-continental migratory routes. Finally, we detected high levels of virus gene segment reassortment, with a high diversity of AIV genome constellations across years and locations. These data, in addition to those from other studies in Africa and South America, clearly show that patterns of AIV dynamics in the Southern Hemisphere are distinct from those in the temperate north., Competing Interests: The authors have declared that no competing interests exist.

The bacterial quorum sensing (QS) system is a target for non-lethal antibacterial agents that do not encourage the development of resistance. QS inhibitors commonly contain a polar "head" moiety and a lipidic "tail" moiety. In this work, we synthesised novel QS inhibitor candidates in which the lipidic "tail" is decorated with stereospecifically positioned fluorine atoms. The presence of fluorine is shown to bias the molecules into distinctive conformations that are pre-organised for binding to the QS receptor. This translates into significant increases in QS inhibitory potency.

Bismuth(III) oxide-carbodiimide (Bi 2 O 2 NCN) has been recently discovered as a novel mixed-anion semiconductor, which is structurally related to bismuth oxides and oxysulfides. Given the structural versatility of these layered structures, we investigated the unexplored photochemical properties of the target compound for photoelectrochemical (PEC) water oxidation. Although Bi 2 O 2 NCN does not generate a noticeable photocurrent as a single photoabsorber, the fabrication of heterojunctions with the WO 3 thin film electrode shows an upsurge of current density from 0.9 to 1.1 mA cm -2 at 1.23 V vs reversible hydrogen electrode (RHE) under 1 sun (AM 1.5G) illumination in phosphate electrolyte (pH 7.0). Mechanistic analysis and structural analysis using powder X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and scanning transmission electron microscopy energy-dispersive X-ray spectroscopy (STEM EDX) indicate that Bi 2 O 2 NCN transforms during operating conditions in situ to a core-shell structure Bi 2 O 2 NCN/BiPO 4 . When compared to WO 3 /BiPO 4 , the in situ electrolyte-activated WO 3 /Bi 2 O 2 NCN photoanode shows a higher photocurrent density due to superior charge separation across the oxide/oxide-carbodiimide interface layer. Changing the electrolyte from phosphate to sulfate results in a lower photocurrent and shows that the electrolyte determines the surface chemistry and mediates the PEC activity of the metal oxide-carbodiimide. A similar trend could be observed for CuWO 4 thin film photoanodes. These results show the potential of metal oxide-carbodiimides as relatively novel representatives of mixed-anion compounds and shed light on the importance of the control over the surface chemistry to enable the in situ activation.

Background: Avian influenza viruses (AIVs) are found worldwide in numerous bird species, causing significant disease in gallinaceous poultry and occasionally other species. Surveillance of wild bird reservoirs provides an opportunity to add to the understanding of the epidemiology of AIVs., Methods: This study examined key findings from the National Avian Influenza Wild Bird Surveillance Program over a 5-year period (July 2007-June 2012), the main source of information on AIVs circulating in Australia., Results: The overall proportion of birds that tested positive for influenza A via PCR was 1.9 ± 0.1%, with evidence of widespread exposure of Australian wild birds to most low pathogenic avian influenza (LPAI) subtypes (H1-13, H16). LPAI H5 subtypes were found to be dominant and widespread during this 5-year period., Conclusion: Given Australia's isolation, both geographically and ecologically, it is important for Australia not to assume that the epidemiology of AIV from other geographic regions applies here. Despite all previous highly pathogenic avian influenza outbreaks in Australian poultry being attributed to H7 subtypes, widespread detection of H5 subtypes in wild birds may represent an ongoing risk to the Australian poultry industry., (© 2015 Australian Veterinary Association.)

In 2009, an outbreak of white nodular cutaneous lesions was detected in one of only two known breeding colonies of the critically endangered southern bentwing bat (Miniopterus schreibersii bassanii), at Naracoorte, South Australia. Necropsies were conducted on 10 euthanized bats in September 2009. In October 2009, 123 bats were examined under anesthesia, with skin biopsies collected from 18 affected bats. Prevalence of skin lesions was 45.2%. The prevalence among males was three times greater than among females. The majority of lesions examined histologically were granulomas, typically centered on a nematode. A single lesion had epidermal hyperplasia with intracytoplasmic inclusions consistent with a pox virus; pox virions were identified on electron microscopy. Nematodes dissected from frozen lesions were identified morphologically as Riouxgolvania beveridgei, previously described in the eastern bentwing bat (Miniopterus schreibersii oceanensis). The factors contributing to this apparent disease emergence and outbreak remain undetermined. Lesions consistent with white nose syndrome were not identified.

Foot and mouth disease (FMD) is endemic in African buffalo (Syncerus caffer) in the Kruger National Park (KNP) and surrounding game parks in South Africa. The last outbreak of the disease in domestic stock outside the FMD control zone occurred in 1957. Due to the success in containing the disease, the country was accorded zone freedom from FMD without vaccination by the Office International des Epizooties (OIE: World organisation for animal health) in 1995. This status was lost in September 2000 when the first-ever recorded case of serotype O in South Africa was diagnosed in a piggery in KwaZulu-Natal after the illegal feeding of untreated swill. In November 2000, an outbreak of FMD caused by serotype South African Territories (SAT) 1 was diagnosed in a feedlot within the free zone of Mpumalanga Province. The SAT 1 outbreak was traced to cattle in the FMD control zone south of the KNP after the game-proof fence surrounding the KNP was severely damaged by floods. This enabled buffalo to come into direct contact with cattle outside the KNP. A further outbreak caused by SAT 2 was diagnosed within the FMD control zone in February 2001, also as a result of buffalo having escaped from the KNP. All these outbreaks were successfully contained, with the re-instatement of zone freedom from FMD without vaccination by the OIE in May 2002. These outbreaks made it necessary to re-examine the methods of control and containment of FMD that have been practised for many years and which are in line with accepted international practices. The authors describe the rationale for the different control strategies that were followed, the need for a multidisciplinary approach to disease control, the interface between control and technological and diagnostic support and the lessons learned. Some suggestions for future control strategies are also offered.