摘要
本文首次测定和分析缓慢细蚤Leptopsylla segnis(Schonherr,1811)和距细蚤Leptopsylla lauta (Rothschild,1913)的rDNA—ITS2序列,为蚤的分类和系统发育研究提供有意义的基础资料。通过聚合酶链反应(Polymerase chain reaction,PCR)扩增缓慢细蚤L.segnis和距细蚤L.lauta各3个个体的rDNA.ITS2序列,并对扩增产物进行PCR直接测序和分析。结果显示,缓慢细蚤和距细蚤的rDNA.ITS2序列的长度均为309bp;缓慢细蚤序列的CG含量为50.9%~52.1%;距细蚤序列的CG含量为49.5%~50.6%。缓慢细蚤与距细蚤的rDNA—ITS2序列有16个碱基不同,其中7个是颠换,9个为转换,两种细蚤之间有一定差异。
To study the sequences of rDNA-ITS2 in Leptopsylla segnis (Schonherr, 1811 ) and Leptopsylla lauta (Rothschild, 1913) for providing basie information for the researches on siphonaptera phylogenesis. The rDNA-ITS2 sequences in the two species were amplified by PCR, and then sequenced directly and analyzed. The length of rDNA-ITS2 in both L. segnis and L. laura was 309 bp. The contents of base pair CG were 50. 9% -52. 1% in the rDNA-ITS2 sequence of L. segnis, and 49.5% -50. 6% in L. lauta. Sixteen base pairs in L. segnis were different from that in L. lauta, including 7 reverses and 9 conversions, implying a significant difference existed between the two Leptopsylla species.
出处
《寄生虫与医学昆虫学报》
CAS
2012年第3期169-171,共3页
Acta Parasitologica et Medica Entomologica Sinica