Journal Articles

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    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 M
    This 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.
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    Obligate mutualism within a host drives the extreme specialization of a fig wasp genome
    (BioMed Central Ltd, 20/12/2013) Xiao J-H; Yue Z; Jia L-Y; Yang X-H; Niu L-H; Wang Z; Zhang P; Sun B-F; He S-M; Li Z; Xiong T-L; Xin W; Gu H-F; Wang B; Werren JH; Murphy RW; Wheeler D; Niu L-M; Ma G-C; Tang T; Bian S-N; Wang N-X; Yang C-Y; Wang N; Fu Y-G; Li W-Z; Yi SV; Yang X-Y; Zhou Q; Lu C-X; Xu C-Y; He L-J; Yu L-L; Chen M; Zheng Y; Wang S-W; Zhao S; Li Y-H; Yu Y-Y; Qian X-J; Cai Y; Bian L-L; Zhang S; Wang J-Y; Yin Y; Xiao H; Wang G-H; Yu H; Wu W-S; Cook JM; Wang J; Huang D-W
    Background: Fig pollinating wasps form obligate symbioses with their fig hosts. This mutualism arose approximately 75 million years ago. Unlike many other intimate symbioses, which involve vertical transmission of symbionts to host offspring, female fig wasps fly great distances to transfer horizontally between hosts. In contrast, male wasps are wingless and cannot disperse. Symbionts that keep intimate contact with their hosts often show genome reduction, but it is not clear if the wide dispersal of female fig wasps will counteract this general tendency. We sequenced the genome of the fig wasp Ceratosolen solmsi to address this question. Results: The genome size of the fig wasp C. solmsi is typical of insects, but has undergone dramatic reductions of gene families involved in environmental sensing and detoxification. The streamlined chemosensory ability reflects the overwhelming importance of females finding trees of their only host species, Ficus hispida, during their fleeting adult lives. Despite long-distance dispersal, little need exists for detoxification or environmental protection because fig wasps spend nearly all of their lives inside a largely benign host. Analyses of transcriptomes in females and males at four key life stages reveal that the extreme anatomical sexual dimorphism of fig wasps may result from a strong bias in sex-differential gene expression. Conclusions: Our comparison of the C. solmsi genome with other insects provides new insights into the evolution of obligate mutualism. The draft genome of the fig wasp, and transcriptomic comparisons between both sexes at four different life stages, provide insights into the molecular basis for the extreme anatomical sexual dimorphism of this species. © 2013 Xiao et al.; licensee BioMed Central Ltd.