Objective To detect Bartonella spp. nucleic acid from main ectoparasite fleas in rodents and free-living ticks from Alashankou pass, China-Kazakhstan border. Methods Collected fleas and ticks were then identified by morphological features. After species identification, genome DNA was extracted and detected by PCR targeting gltA, ITS and ribC of Bartonella spp. The amplified products were sequenced and the sequences analyzed using the Blast. A phylogenetic tree was constructed using Mega 6.0 software. Results A total 2 139 fleas (7 species, 6 genera) were identified. Xenopsylla minax was the predominant species. A total of 243 free-living ticks were identified as Hyalomma asiaticum. Only X. minax, Coptospllya lamellifer ardua, and Parddoxopsyllus repandustested positive for Bartonella spp. and all the ticks were negative. Sequence analysis showed that three different sequences, DNAman homology were 93.61%, 52.54%, and 86.72%, respective, gltA, ITS, and ribC. Blast and phylogenetic analyses showed that this three Bartonella and Bartonella sp. AL01,02, 04 were same sequence. Conclusion Bartonella nucleic acid was detected in three different wild rat-flea species at Alashankou pass.
YIN Xiao-ping, ZHAO Shan-shan, TIAN Yan-he, BA Te, ZHANG Jiang-guo, CHENG Tian-li, WANG Yuan-zhi
. Detection of Bartonella from rodent-harboring fleas and free-living ticks at Alashankou pass,China-Kazakhstan border[J]. Chinese Journal of Vector Biology and Control, 2017
, 28(4)
: 350
-353
.
DOI: 10.11853/j.issn.1003.8280.2017.04.011
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