Anaplasma and Ehrlichia are important emerging tick-borne pathogens in both humans and animals. Here, we conducted a molecular surveillance study in Gansu, China to assess the prevalence of Anaplasma and Ehrlichia spp. in red deer and sika deer based on polymerase chain reaction (PCR) analysis and sequencing of 16S rRNA or msp genes. PCR revealed that the prevalence of Anaplasma ovis, Anaplasma bovis and Anaplasma platys of the Qilian Mountain samples was 32%, 9% and 9%, respectively; the prevalence of Anaplasma ovis, Anaplasma bovis, Anaplasma platys was 20%, 15% and 15% among the Long Mountain samples, respectively. Of the Long Mountain samples, two (5%) of the 40 samples were positive for Ehrlichia canis, but all 44 of the Qilian Mountain samples were negative for E. canis, and no other Anaplasma or Ehrlichia spp. were found in the samples. The phylogenetic tree showed that the newly isolated Anaplasma and Ehrlichia spp. could be classified as belonging to four clades, including an A. bovis cluster, A. ovis cluster, A. platys cluster and E. canis cluster. In addition, Bartonella schoenbuchensis was firstly identified in blood samples from red deer in Gansu, China. Our results provide important data to increase the understanding of the epidemiology of anaplasmosis and ehrlichiosis of red deer and sika deer and will assist with the implementation of measures to control anaplasmosis and ehrlichiosis transmission to red deer, sika deer and other animals in Gansu, China.
Ageratina adenophora is one of the most hazardous invasive weeds in China. It can form a single species community quickly and cause extensive ecological harm. The belowground microbial community can participate in nutrient transformation in soil and plays an important role in the invasiveness of exotic plant species. We selected sampling sites with different invasion levels of A. adenophora. The soil property and soil biogeochemical activity were measured in both bulk and rhizosphere soil under the aggressive weed A. adenophora and under adjacent native plants. The composition of bacterial communities was investigated using high‐throughput 16S rRNA gene sequencing. We found that the rhizosphere habitat selectively accumulated Sphingomonas and Steroidobacter and reduced the abundance of Gaiella and Gp6 regardless of plant host. The presence of A. adenophora caused a switch in microbial composition from Aeromicrobium and Marmoricola to Reyranella and Bradyrhizobium in the bulk soil, and from Gp4, Pirellula, Lysobacter and Aridibacterrae to Reyranella and Streptomyces in the rhizosphere soil. We also revealed specific microbes that closely related with N‐cycling processes. In addition, soil pH was the main factor affecting microbial communities in both bulk and rhizosphere soil. Our study confirmed that the rhizosphere environment imposed homogenous microbial communities. The invasion of A. adenophora selected specialized bacterial communities in soils and specific microbes that potentially mediated soil nutrition cycling. Our findings provide ecological explanation to explain how the underground microbes help A. adenophora invasive.
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