Centre for Infectious Diseases, Institute for Parasitology and Tropical Veterinary Medicine, Freie Universitaet Berlin, Robert-von-Ostertag-Str. 7-13, 14163, Berlin, Germany,
Parasitol Res. 2014 Feb;113(2):723-6. doi: 10.1007/s00436-013-3701-z. Epub 2013 Nov 29.
Riverine tsetse (Glossina) as Glossina palpalis gambiensis Vanderplank 1949 and Glossina tachinoides Westwood 1850 are the main vectors for African animal trypanosomoses in Burkina Faso. Vector control has been proven efficient in disease containment, but its success is endangered by the reinvasion of tsetse from neighbouring areas. Thus, identifying relic populations can enhance the success rate of vector control efforts. This is currently carried out through microsatellite analysis which is time-consuming and costly. Recently, matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry-based analysis has become a routine method in microbial species identification. Owing to the rapidness and cost-effectiveness, this approach has been extended towards species identification of higher organisms such as tsetse. Following the recent experiences in distinguishing two genotypes of Prototheca spp., it is of interest to explore the validity of mass spectrometry for tsetse population differentiation. As a preliminary test, we submitted male and female G. palpalis gambiensis and G. tachinoides from Sideradougou and Folonzo, Burkina Faso (distance 60 km) to matrix-assisted laser desorption/ionisation analysis. The wing samples were utilized for protein extraction and mass spectra in a broad mass to charge ratio (2,000-20,000 kDa) were obtained. Specific peaks appeared to represent species, sex and location. Then, a peak list was extracted, containing the peaks in mass-to-charge ratio by revealing their intensities as well. These lists were used to compute a spectral dendrogram and a principle component analysis which displayed the differences among the samples from the two different regions. The results indicate that this technique can be extended with additional tsetse species, ideally with supporting genomic data, to later assist in designing rational vector control strategies.
河栖采采蝇( Glossina ),包括 Glossina palpalis gambiensis Vanderplank 1949 和 Glossina tachinoides Westwood 1850,是布基纳法索非洲动物锥虫病的主要传播媒介。实践证明,通过控制媒介可以有效控制疾病,但采采蝇从邻近地区重新入侵会威胁到控制媒介的成功,因此,确定残余种群可以提高控制媒介努力的成功率。目前,这是通过微卫星分析来完成的,这种方法既耗时又昂贵。最近,基于基质辅助激光解吸/电离飞行时间质谱分析的方法已成为微生物物种鉴定的常规方法。由于快速和具有成本效益,这种方法已扩展到对较高生物体(如采采蝇)的物种鉴定。鉴于最近在区分两种 Prototheca spp. 基因型方面的经验,探索质谱法用于采采蝇种群分化的有效性是很有意义的。作为初步测试,我们提交了来自布基纳法索 Sideradougou 和 Folonzo 的雄性和雌性 G. palpalis gambiensis 和 G. tachinoides(距离 60 公里)进行基质辅助激光解吸/电离分析。利用翅膀样本进行蛋白质提取,并在较宽的质荷比(2000-20000 kDa)范围内获得质谱。似乎出现了特定的峰代表物种、性别和位置。然后,提取峰列表,包含质荷比中的峰,并揭示其强度。这些列表用于计算光谱树状图和主成分分析,以显示来自两个不同区域的样本之间的差异。结果表明,该技术可以通过增加其他采采蝇物种来扩展,理想情况下还需要支持基因组数据,以帮助设计合理的媒介控制策略。