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Item A novel gyrovirus is abundant in yellow-eyed penguin (Megadyptes antipodes) chicks with a fatal respiratory disease.(2023-02) Wierenga JR; Morgan KJ; Hunter S; Taylor HS; Argilla LS; Webster T; Dubrulle J; Jorge F; Bostina M; Burga L; Holmes EC; McInnes K; Geoghegan JLYellow-eyed penguins (Megadyptes antipodes), or hoiho in te reo Māori, are predicted to become extinct on mainland Aotearoa New Zealand in the next few decades, with infectious disease a significant contributor to their decline. A recent disease phenomenon termed respiratory distress syndrome (RDS) causing lung pathology has been identified in very young chicks. To date, no causative pathogens for RDS have been identified. In 2020 and 2021, the number of chick deaths from suspected RDS increased four- and five-fold, respectively, causing mass mortality with an estimated mortality rate of >90%. We aimed to identify possible pathogens responsible for RDS disease impacting these critically endangered yellow-eyed penguins. Total RNA was extracted from tissue samples collected during post-mortem of 43 dead chicks and subject to metatranscriptomic sequencing and histological examination. From these data we identified a novel and highly abundant gyrovirus (Anelloviridae) in 80% of tissue samples. This virus was most closely related to Gyrovirus 8 discovered in a diseased seabird, while other members of the genus Gyrovirus include Chicken anaemia virus, which causes severe disease in juvenile chickens. No other exogenous viral transcripts were identified in these tissues. Due to the high relative abundance of viral reads and its high prevalence in diseased animals, it is likely that this novel gyrovirus is associated with RDS in yellow-eyed penguin chicks.Item CHANGES IN THE LEVELS OF THEILERIA ORIENTALIS IKEDA TYPE INFECTION IN HAEMAPHYSALIS LONGICORNIS NYMPHS OVER A SIX-MONTH PERIOD.(1/09/2021) Zhao Y; Lawrence KE; Minor M; Gedye K; Wang B; Pomroy W; Potter MThis study aimed to investigate whether the infection intensity of Theileria orientalis Ikeda type organisms within Haemaphysalis longicornis larvae and nymph stages fluctuated over 6 mo after feeding as larvae on infected calves in the field. Naïve larvae, hatched from eggs, were fed on infected calves for 5 days while contained within cotton socks glued over the calves' ears. Larvae were first sampled immediately post-feeding and then sampled every 3 wk for 23 wk in total, after molting to nymphs. All larvae and nymphs were tested for T. orientalis Ikeda organisms using quantitative PCR. The qPCR results showed that the infection intensity of Haemaphysalis longicornis larvae and nymphs was not constant over the sampling period, and after initially dropping after molting to nymphs, it then rose with fasting to a maximum at 17 and 23 wk post-feeding. The significant rise in T. orientalis Ikeda organisms observed at 23 wk postfeeding may explain why more severe clinical cases of bovine theileriosis in New Zealand are seen in the spring when nymphs are the predominant instar questing.Item BfpI, BfpJ, and BfpK Minor Pilins Are Important for the Function and Biogenesis of Bundle-Forming Pili Expressed by Enteropathogenic Escherichia coli(American Society for Microbiology, 1/03/2016) Nisa S; Martinez de la Peña CF; De Masi L; Mulvey G; Tong J; Donnenberg MS; Armstrong GDItem The population genetic structure of the urchin Centrostephanus rodgersii in New Zealand with links to Australia(1/09/2021) Thomas LJ; Liggins L; Banks SC; Beheregaray LB; Liddy M; McCulloch GA; Waters JM; Carter L; Byrne M; Cumming RA; Lamare MDThe diadematid sea urchin Centrostephanus rodgersii occurs in Australia and New Zealand and has undergone recent southward range extension in Australia as a result of regional warming. Clarifying the population genetic structure of this species across its New Zealand range would allow a better understanding of recent and future mechanisms driving range changes in the species. Here, we use microsatellite DNA data to assess connectivity and genetic structure in 385 individuals from 14 locations across the Australian and New Zealand ranges of the species. We detected substantial genetic differentiation among C. rodgersii populations from Australia and New Zealand. However, the population from Port Stephens (located north of Newcastle), Australia, strongly clustered with New Zealand samples. This suggests that the New Zealand populations recently originated from this area, likely via larval transport in the Tasman Front flow that arises in this region. The weak population genetic structure and relatively low genetic diversity detected in New Zealand (global Fst = 0.0021) relative to Australia (global Fst = 0.0339) is consistent with the former population’s inferred history of recent climate-driven expansion. Population-level inbreeding is low in most populations, but were higher in New Zealand (global Fis = 0.0833) than in Australia (global Fis = 0.0202), suggesting that self-recruitment is playing an increasingly important role in the New Zealand region. Our results suggest that C. rodgersii is likely to spread southwards as ocean temperatures increase; therefore, it is crucial that researchers develop a clearer understanding of how New Zealand ecosystems will be reshaped by this species (and others) under climate change.Item Papillomaviruses in dogs and cats.(2017-07) Munday JS; Thomson NA; Luff JAPapillomaviruses (PVs) cause disease in both dogs and cats. In dogs, PVs are thought to cause oral papillomatosis, cutaneous papillomas and canine viral pigmented plaques, whereas PVs have been rarely associated with the development of oral and cutaneous squamous cell carcinomas in this species. In cats, PVs are currently thought to cause oral papillomas, feline viral plaques, Bowenoid in situ carcinomas and feline sarcoids. Furthermore, there is increasing evidence that PVs may also be a cause of cutaneous squamous cell carcinomas and basal cell carcinomas in cats. These diseases are discussed in this review. Additionally, there is a brief overview of PV biology, including how these viruses cause disease. Diagnostic techniques and possible methods to prevent PV infection are also discussed.Item Genetic diversity targets and indicators in the CBD post-2020 Global Biodiversity Framework must be improved(Elsevier Ltd, 2020-08) Hoban S; Bruford M; D'Urban Jackson J; Lopes-Fernandes M; Heuertz M; Hohenlohe PA; Paz-Vinas I; Sjögren-Gulve P; Segelbacher G; Vernesi C; Aitken S; Bertola LD; Bloomer P; Breed M; Rodríguez-Correa H; Funk WC; Grueber CE; Hunter ME; Jaffe R; Liggins L; Mergeay J; Moharrek F; O'Brien D; Ogden R; Palma-Silva C; Pierson J; Ramakrishnan U; Simo-Droissart M; Tani N; Waits L; Laikre LThe 196 parties to the Convention on Biological Diversity (CBD) will soon agree to a post-2020 global framework for conserving the three elements of biodiversity (genetic, species, and ecosystem diversity) while ensuring sustainable development and benefit sharing. As the most significant global conservation policy mechanism, the new CBD framework has far-reaching consequences- it will guide conservation actions and reporting for each member country until 2050. In previous CBD strategies, as well as other major conservation policy mechanisms, targets and indicators for genetic diversity (variation at the DNA level within species, which facilitates species adaptation and ecosystem function) were undeveloped and focused on species of agricultural relevance. We assert that, to meet global conservation goals, genetic diversity within all species, not just domesticated species and their wild relatives, must be conserved and monitored using appropriate metrics. Building on suggestions in a recent Letter in Science (Laikre et al., 2020) we expand argumentation for three new, pragmatic genetic indicators and modifications to two current indicators for maintaining genetic diversity and adaptive capacity of all species, and provide guidance on their practical use. The indicators are: 1) the number of populations with effective population size above versus below 500, 2) the proportion of populations maintained within species, 3) the number of species and populations in which genetic diversity is monitored using DNA-based methods. We also present and discuss Goals and Action Targets for post-2020 biodiversity conservation which are connected to these indicators and underlying data. These pragmatic indicators and goals have utility beyond the CBD; they should benefit conservation and monitoring of genetic diversity via national and global policy for decades to come.Item Different effects of grazing and nitrogen addition on ecosystem multifunctionality are driven by changes in plant resource stoichiometry in a typical steppe(5/08/2022) Li L; He XZ; Zhang X; Hu J; Wang M; Wang Z; Hou FPurpose: Herbivore grazing and nitrogen (N) input may alter the multiple ecosystem functions (i.e., multifunctionality, hereafter) associated with carbon (C), N, and phosphorus (P) cycling. Most studies on variations in plant diversity, soil biotic or abiotic factors, and linkages to ecosystem functions have focused on grazing or N enrichment alone. Few studies have combined these two factors to explore the role of plant resource stoichiometry (C:N:P ratios) in ecosystem multifunctionality (EMF) control. Here, we evaluated the direct and indirect effects of stocking rate (0, 2.7, 5.3, and 8.7 sheep ha− 1) and N addition rate (0, 5, 10, and 20 g N m− 2 yr− 1) on a range of ecosystem functions and EMF via changing plant diversity, soil pH and plant resource stoichiometry in a typical steppe on the Loess Plateau. Results: We found that increasing stocking rate and interaction between grazing and N addition significantly decreased EMF, while increasing N addition rate significantly promoted EMF. Grazing decreased soil NH4+-N, soil NO3−-N, aboveground biomass, and plant C, N, and P pools, but increased soil total N and P at 8.7 and 5.3 sheep ha− 1, respectively. N addition increased soil NH4+-N, NO3−-N, and total P. Plant aboveground biomass, and plant C, N, and P pools increased at the lower N addition rate (≤ 5 g N m− 2 yr− 1) under grazing. The structural equation models indicated that (1) EMF was driven by the direct effects of grazing and the indirect effects of grazing on plant resource stoichiometry and soil pH; (2) EMF increased with increasing N addition rates, but such positive response of EMF to increasing N addition rates was alleviated at high levels of plant resource stoichiometry and diversity; and (3) the indirect effects of plant diversity induced by grazing and N addition had moderate effects on EMF via the variations of plant resource stoichiometry. Conclusions: This study demonstrated grazing and N addition had contrasting effects on ecosystem multifunctionality in a typical steppe, and highlighted the capacity of plant diversity in balancing plant elements that serve as a key mechanism in the maintenance of EMF in response to intensive grazing and N enrichment.Item Environmental input-output analysis of the New Zealand dairy industry(Inderscience Enterprises Ltd., 2/01/2012) Flemmer CL; Nepomuceno-Silo, JThis work presents data and analysis quantifying the total (direct and indirect) resource use and outputs (products and pollutants) of the New Zealand dairy industry for the year April 1997 to March 1998. It also identifies those sectors supplying the dairy industry which make significant indirect contributions to its total inputs and outputs. Although this data is 14 years old, it is the only large-scale, detailed data available. Further, more modern data can be compared with this baseline data. Comparison with the other major New Zealand food and fibre sectors shows that the dairy farming sector has the highest total water consumption and the highest total effluent. It also has high total land use, electricity use and production of animal methane. The dairy processing sector is water and fuel intensive and has high total water effluent and greenhouse gas emissions. The high resource use and pollutants have to be weighed against the enormous economic value of the dairy sectors.Item Geostatistical determination of soil noise and soil phosphorus spatial variability(Elsevier Masson, 28/09/2017) Kaul TMC; Grafton MCEThis research studies the effect of stratifying soil samples to try and find a suitable depth to establish a geospatial relationship for a practical soil sampling grid in New Zealand hill country. Cores were collected from 200 predetermined sites in grids at two trial sites at “Patitapu” hill country farm in theWairarapa, New Zealand. Trial 1 was a 200 m 100 m grid located in a gently undulating paddock. Trial 2 was a 220 m 80 m grid located on a moderately sloped paddock. Each grid had cores taken at intervals of 5 m, 10 m, or 20 m. Core sites were mapped out prior to going into the field; these points were found using a Leica Geo Systems GS15 (real time kinematic GPS) and marked with pigtail pegs and spray-paint on the ground. Cores were taken using a 50 mm-diameter soil core sampler. Cores were cut into three sections according to depth: A—0–30 mm, B—30–75 mm, and C—75–150 mm. Olsen P lab results were obtained for half of the total 1400 samples due to financial constraints. The results indicate that there was a significant decrease in variability from Section A to Section B for both trials. Section B and C for Trial 1 had similar variability, whereas there was another significant drop in variability from Section B to C in Trial 2. Measuring samples below the top 3 cm appeared to effectively reduce noise when sampled from 3 to 15 cm. However, measuring from 7.5 cm to 15 cm on the slope in Trial 2 reduced variability so much that all results were almost identical, which may mean that there is no measurable representation of plant available P. The reduction in noise by removing the top 3 cm of soil samples is significant for improving current soil nutrient testing methods by allowing better geospatial predictions for whole paddock soil nutrient variability mappingItem Bistability in a metabolic network underpins the De Novo evolution of colony switching in Pseudomonas fluorescens(PUBLIC LIBRARY SCIENCE, 12/03/2015) Gallie J; Libby E; Bertels F; Remigi P; Jendresen CB; Ferguson GC; Desprat N; Buffing MF; Sauer U; Beaumont HJE; Martinussen J; Kilstrup M; Rainey PB© 2015 Gallie et al. Phenotype switching is commonly observed in nature. This prevalence has allowed the elucidation of a number of underlying molecular mechanisms. However, little is known about how phenotypic switches arise and function in their early evolutionary stages. The first opportunity to provide empirical insight was delivered by an experiment in which populations of the bacterium Pseudomonas fluorescens SBW25 evolved, de novo, the ability to switch between two colony phenotypes. Here we unravel the molecular mechanism behind colony switching, revealing how a single nucleotide change in a gene enmeshed in central metabolism (carB) generates such a striking phenotype. We show that colony switching is underpinned by ON/OFF expression of capsules consisting of a colanic acid-like polymer. We use molecular genetics, biochemical analyses, and experimental evolution to establish that capsule switching results from perturbation of the pyrimidine biosynthetic pathway. Of central importance is a bifurcation point at which uracil triphosphate is partitioned towards either nucleotide metabolism or polymer production. This bifurcation marks a cell-fate decision point whereby cells with relatively high pyrimidine levels favour nucleotide metabolism (capsule OFF), while cells with lower pyrimidine levels divert resources towards polymer biosynthesis (capsule ON). This decision point is present and functional in the wild-type strain. Finally, we present a simple mathematical model demonstrating that the molecular components of the decision point are capable of producing switching. Despite its simple mutational cause, the connection between genotype and phenotype is complex and multidimensional, offering a rare glimpse of how noise in regulatory networks can provide opportunity for evolution.
