GLOBAL HARMONISATION IN THE FIELD OF INVASIVE SPECIES MANAGEMENT PRODUCT DEVELOPMENT

Problems associated with managing vertebrate invasive species, defined as any exotic or native species that has spread beyond its natural range, are remarkably common around the world. Although the species may differ, the niches they fill and the damage they generally cause is often consistent. As such, a possibility exists for greater collaboration and harmonization in developing new tools to manage the impacts of invasive species. Moreover, the considerable expense of developing new products, the often onerous registration process, and the lack of return on investment leading to market failure has meant that progress within the field of invasive animal management product development can sometimes be stifled. This paper details a potential way forward using specific examples of ways the Invasive Animals Cooperative Research Centre (IACRC), Pestat P/L, and other IACRC commercial partners aim to provide overseas organizations with humane non-lethal and lethal wildlife management tools. Conversely, we detail overseas-developed products currently being tested in Australia, and a proposal to keep abreast of new developments in other countries to ensure invasive species management within Australasia remains of the highest level. This can only be achieved through truly collaborative research and the global harmonization of registration packages, so product development costs can be minimized and the necessary scales of production can be attained

Low Secondary Risks for Captive Coyotes from a Sodium Nitrite Toxic Bait for Invasive Wild Pigs

An acute toxic bait is being developed to deliver micro‐encapsulated sodium nitrite (SN) to stimulate severe methemoglobinemia and humane death for invasive wild pigs (Sus scrofa), thereby providing a new tool for reducing their populations. During April 2016, we evaluated sensitivity to SN and outcomes of secondary consumption in the ubiquitous mammalian scavenger, coyote (Canis latrans), to determine secondary risks of consuming carcasses of wild pigs that died from consuming the SN toxic bait. At the National Wildlife Research Center in Fort Collins, Colorado, USA, we first evaluated whether coyotes fed carcasses of domestic pigs killed by consumption of SN bait showed signs of SN intoxication. Second, we conducted chemical analysis of residual SN in the coyotes for evidence of SN passing from pigs to coyotes. Last, we conducted an acute oral toxicity test (LD50) with SN for coyotes by feeding them meatballs containing capsules of SN. We found no evidence that captive coyotes experienced SN intoxication from consuming on carcasses that had been freshly poisoned with SN, despite consuming ¯ x = 1.6 kg of tissues/coyote within 24 hours. None of the captive coyotes consumed digestive tracts or stomach contents from poisoned carcasses, which contained the highest levels of residual SN. Chemical analysis indicated that only ≤34.14 mg/kg of residual SN were passed from the tissues of the pigs into the coyotes, confirming that SN does not bioaccumulate. All coyotes quickly vomited various doses of SN during the LD50 test and fully recovered, suggesting a natural defense against secondary poisoning from SN. Testing with captive coyotes indicates that the risks of secondary poisoning for free‐ranging coyotes are likely low, although field‐testing should be used to confirm

Low Secondary Risks for Captive Coyotes from a Sodium Nitrite Toxic Bait for Invasive Wild Pigs

An acute toxic bait is being developed to deliver micro‐encapsulated sodium nitrite (SN) to stimulate severe methemoglobinemia and humane death for invasive wild pigs (Sus scrofa), thereby providing a new tool for reducing their populations. During April 2016, we evaluated sensitivity to SN and outcomes of secondary consumption in the ubiquitous mammalian scavenger, coyote (Canis latrans), to determine secondary risks of consuming carcasses of wild pigs that died from consuming the SN toxic bait. At the National Wildlife Research Center in Fort Collins, Colorado, USA, we first evaluated whether coyotes fed carcasses of domestic pigs killed by consumption of SN bait showed signs of SN intoxication. Second, we conducted chemical analysis of residual SN in the coyotes for evidence of SN passing from pigs to coyotes. Last, we conducted an acute oral toxicity test (LD50) with SN for coyotes by feeding them meatballs containing capsules of SN. We found no evidence that captive coyotes experienced SN intoxication from consuming on carcasses that had been freshly poisoned with SN, despite consuming ¯ x = 1.6 kg of tissues/coyote within 24 hours. None of the captive coyotes consumed digestive tracts or stomach contents from poisoned carcasses, which contained the highest levels of residual SN. Chemical analysis indicated that only ≤34.14 mg/kg of residual SN were passed from the tissues of the pigs into the coyotes, confirming that SN does not bioaccumulate. All coyotes quickly vomited various doses of SN during the LD50 test and fully recovered, suggesting a natural defense against secondary poisoning from SN. Testing with captive coyotes indicates that the risks of secondary poisoning for free‐ranging coyotes are likely low, although field‐testing should be used to confirm

Development of Toxic Bait to Control Invasive Wild Pigs and Reduce Damage

Populations of invasive wild pigs (Sus scrofa) are increasing in many regions of the world, in particular the United States and Australia. Invasive wild pigs cause extensive damage to ecological resources and agriculture. Development and registration of a safe and humane toxic bait offers a practical and cost effective tool to control invasive species. Currently, no toxicants are approved for use on invasive wild pigs in the United States and those approved in Australia are under scrutiny because of concerns regarding humaneness and effects on nontarget species. We tested a newly formulated bait containing the microencapsulated active ingredient, sodium nitrite (HOGGONE®; Animal Control Technologies Australia P/L, Victoria, Australia), that is considered humane and safer for nontarget species because it does not bioaccumulate. We examined palatability, lethality, and stability of the bait (i.e., fresh compared to 8-monthold bait) on groups of captive invasive wild pigs. We found HOGGONE® was a preferred food item, averaging 475 g of toxic bait consumed per animal during the first night offered. Consumption of HOGGONE® resulted in 95% mortality (53 of 56) in the treatment groups across 2 treatment nights. Most mortalities (98%) occurred during the first night the toxic bait was offered. Camera evidence suggested that deaths occurred within 3 hr post-offering. The toxic bait was stable and effective up to 8 months post manufacture. Our results support current applications to register HOGGONE® for reducing damage from invasive wild pigs in the United States and Australia. Further research is required to evaluate HOGGONE® on free-ranging invasive wild pigs using bait stations that exclude nontarget species

Recognising potential for preventing hospitalisation

To identify the incidence and distribution of public hospital admissions in South Australia that could potentially be prevented with appropriate use of primary care services, analysis was completed of all public hospital separations from July 2006 to June 2008 in SA. This included those classified as potentially preventable using the Australian Institute of Health and Welfare criteria for selected potentially preventable hospitalisations (SPPH), by events and by individual, with statistical local area geocoding and allocation of relative socioeconomic disadvantage quintile. A total of 744 723 public hospital separations were recorded, of which 79 424 (10.7%) were classified as potentially preventable. Of these, 59% were for chronic conditions, and 29% were derived from the bottom socioeconomic status (SES) quintile. Individuals in the lowest SES quintile were 2.5 times more likely to be admitted for a potentially preventable condition than those from the top SES quintile. Older individuals, males, those in the most disadvantaged quintiles, non-metropolitan areas and Indigenous people were more likely to have more than one preventable admission. People living in more disadvantaged areas in SA appear to have poorer utilisation of effective primary care, resulting in preventable hospital admissions, than those in higher SES groups. The SA Health Care Plan, 2007-2016 is aimed at investing in improved access to primary care in those areas of most disadvantage. The inclusion of SPPHs in future routine reporting should identify if this has occurred

Bait Preference of Free-Ranging Feral Swine for Delivery of a Novel Toxicant

Invasive feral swine (Sus scrofa) cause extensive damage to agricultural and wildlife resources throughout the United States. Development of sodium nitrite as a new, orally delivered toxicant is underway to provide an additional tool to curtail growth and expansion of feral swine populations. A micro-encapsulation coating around sodium nitrite is used to minimize detection by feral swine and maximize stability for the reactive molecule. To maximize uptake of this toxicant by feral swine, development a bait matrix is needed to 1) protect the micro-encapsulation coating so that sodium nitrite remains undetectable to feral swine, 2) achieve a high degree of acceptance by feral swine, and 3) be minimally appealing to non-target species. With these purposes, a field evaluation at 88 sites in south-central Texas was conducted using remote cameras to evaluate preferences by feral swine for several oil-based bait matrices including uncolored peanut paste, black-colored peanut paste, and peanut-based slurry mixed onto whole-kernel corn. These placebo baits were compared to a reference food, whole-kernel corn, known to be readily taken by feral swine (i.e., control). The amount of bait consumed by feral swine was also estimated using remote cameras and grid boards at 5 additional sites. On initial exposure, feral swine showed reduced visitations to the uncolored peanut paste and peanut slurry treatments. This reduced visitation subsided by the end of the treatment period, suggesting that feral swine needed time to accept these bait types. The black-colored peanut paste was visited equally to the control throughout the study, and enough of this matrix was consumed to deliver lethal doses of micro-encapsulated sodium nitrite to most feral swine during 1–2 feeding events. None of the treatment matrices reduced visitations by nontarget species, but feral swine dominated visitations for all matrices. It was concluded that black-colored peanut paste achieved satisfactory preference and consumption by feral swine, and no discernable preference by non-target species, compared to the other treatments

A high-throughput sequencing assay to comprehensively detect and characterize unicellular eukaryotes and helminths from biological and environmental samples

Abstract Background Several of the most devastating human diseases are caused by eukaryotic parasites transmitted by arthropod vectors or through food and water contamination. These pathogens only represent a fraction of all unicellular eukaryotes and helminths that are present in the environment and many uncharacterized organisms might have subtle but pervasive effects on health, including by modifying the microbiome where they reside. Unfortunately, while we have modern molecular tools to characterize bacterial and, to a lesser extent, fungal communities, we lack suitable methods to comprehensively investigate and characterize most unicellular eukaryotes and helminths: the detection of these organisms often relies on microscopy that cannot differentiate related organisms, while molecular assays can only detect the pathogens specifically tested. Results Here, we describe a novel sequencing-based assay, akin to bacterial 16S rRNA sequencing, that enables high-throughput detection and characterization of a wide range of unicellular eukaryotes and helminths, including those from taxonomical groups containing all common human parasites. We designed and evaluated taxon-specific PCR primer pairs that selectively amplify all species from eight taxonomical groups (Apicomplexa, Amoeba, Diplomonadida, Kinetoplastida, Parabasalia, Nematoda, Platyhelminthes, and Microsporidia). We then used these primers to screen DNA extracted from clinical, biological, and environmental samples, and after next-generation sequencing, identified both known and previously undescribed organisms from most taxa targeted. Conclusions This novel high-throughput assay enables comprehensive detection and identification of eukaryotic parasites and related organisms, from a wide range of complex biological and environmental samples. This approach can be easily deployed to many settings and will efficiently complement existing methods and provide a holistic perspective on the microbiome

^99mTc-DMSA scintigraphy.

<p>Results from ^99mTc-DMSA scintigraphy performed 4, 8, and 12 months after ¹⁷⁷Lu-octreotate administration. The kidney uptake is presented as percent of injected activity normalized to controls. Error bars represent SEM and * indicates statistically significant difference compared with controls (p<0.05)</p