Elephant Endotheliotropic Herpesvirus 1, 4 and 5 in China: Occurrence in Multiple Sample Types and Implications for Wild and Captive Population Surveillance.

Elephant endotheliotropic herpesviruses (EEHVs) are important causes of death in both captive and wild Asian elephants (Elephas maximus). Nothing is known about the prevalence of EEHVs in wild or domestic elephants in China. To determine if EEHVs are present in elephants in China, 126 wild elephants from three populations and 202 captive individuals from zoos (n = 155) and the Wild Elephant Valley (n = 47) were screened using semi-nested polymerase chain reaction assays with EEHV-redundant and EEHV1/4/5-specific primers. EEHV1B and EEHV4 were detected in samples from both wild (EEHV1B:8/126; EEHV4:2/126) and captive (EEHV1B:5/155; EEHV4:9/155) elephants, while EEHV1A (six cases) and EEHV5 (one case) were only present in the captive elephants from the Wild Elephant Valley. EEHV1 was detected in blood and trunk and oral swabs; EEHV4 was detected in trunk and oral swabs as well as feces; EEHV5 was found in trunk and oral swabs. No significant age or sex association with EEHV1A, EEHV1B, or EEHV5 positivity was observed. An age association with EEHV4 positivity was found, with all unweaned elephants being EEHV4 positive, but an association with the sex of the elephant was not observed. These findings represent the first documentation of EEHV presence in captive and wild elephants in China. These findings also document EEHV1B and EEHV4 shedding in feces and demonstrate the utility of fecal screening as a tool for investigating EEHV4 infection in wild populations of elephants. It is recommended that EEHV testing be included in surveillance programs for captive and wild elephants in China.

Raging elephants: effects of human disturbance on physiological stress and reproductive potential in wild Asian elephants.

Human disturbance has become a widespread threat to wildlife viability. The Asian elephant (Elephas maximus), an endangered and disturbance-prone species, is under severe threat from habitat loss and fragmentation, human-elephant conflict and poaching. Establishing connections between human disturbance, stress responses and reproduction is crucial for assessing the long-term survivability of a species and will provide critical information for conservation management. The current study investigated the effects of human disturbance on population-level stress responses and stress-related effects on reproductive potential of wild Asian elephants in Xishuangbanna Dai Autonomous Prefecture, China. We used a radioimmunoassay to measure the concentration of fecal cortisol and estradiol in 257 samples collected from five local populations at 15 sites over 4 years. Human disturbance in Xishuangbanna was quantified based on the Ecological-Niche Factor Analysis model. We found that fecal cortisol concentrations were strongly positively correlated with the degree of human disturbance and increased markedly with the expansion of tea plantations. Percentage of non-stressed individuals in a population was higher depending on the extend of undisturbed area in their home ranges. Fecal estradiol concentrations decreased significantly with increasing stress levels. Our results suggest that human disturbance poses environmental challenges to wild Asian elephant populations, and chronic exposure to human disturbance could lead to population decline. The study demonstrates the efficacy of non-invasive endocrine monitoring for further informing management decisions and developing conservation strategies.

[Prokaryotic expression, purification and preparation of polyclonal antibody for wheat grain peroxidase WP1 gene].

Wheat peroxidases 1 (WP1) is the major cationic peroxidase of wheat (Triticum aestivum) grain, which is involved in the development of seeds and an important factor to affect the final processing quality of flour. We constructed a prokaryotic expression vector pET28a-WP1, and transformed it into E. coli host strain T7 Expression. His-tag fused WP1 existed as inclusion body, and the recombinant protein was purified by Ni-NTA resin affinity chromatography under denatured condition. The purity of target protein reached 98%. The recombinant WP1 was refolded by gradient urea dialysis, then used as antigen to immune rabbit to prepare polyclonal antibody. The result of ELISA showed that the titer of rabbit anti-WP1 antiserum was higher than 1:625 000. The result of Western blotting demonstrated that the prepared WP1 polyclonal antibody could be used to detect WP1 with high specificity.