Favia G, Cancrini G, Ricci I, Bazzocchi C, Magi M, Pietrobelli M, Genchi C, Bandi C
Istituto di Patologia Generale Veterinaria dell'Università degli Studi di Milano, via Celoria 10, Milano, 20133, Italy.
Mol Cell Probes. 2000 Oct;14(5):285-90. doi: 10.1006/mcpr.2000.0317.
We have amplified by PCR the sequences of the 5 S ribosomal spacer of Setaria labiatopapillosa and Foleyella furcata. After sequencing, these sequences have been compared with those of Dirofilaria immitis and Dirofilaria repens. Two major goals have been achieved: (i) the establishment of a multiplex PCR-based diagnostic assay, applicable to identify the four species in vertebrate and invertebrate hosts; (ii) the identification, in S. labiatopapillosa and F. furcata, of a canonical spliced leader 1 (SL1) sequence, so confirming that only D. repens, of the filarial parasites so far studied, shows a peculiar SL1 sequence. The PCR assay here developed and the analysis of the 5 S ribosomal spacer, can further improve both epidemiological and molecular analysis of these filarial species.
我们通过聚合酶链反应(PCR)扩增了唇乳头丝虫(Setaria labiatopapillosa)和叉尾丝虫(Foleyella furcata)的5S核糖体间隔区序列。测序后,将这些序列与犬恶丝虫(Dirofilaria immitis)和匐行恶丝虫(Dirofilaria repens)的序列进行了比较。已实现两个主要目标:(i)建立基于多重PCR的诊断检测方法,适用于在脊椎动物和无脊椎动物宿主中鉴定这四种丝虫;(ii)在唇乳头丝虫和叉尾丝虫中鉴定出一个典型的剪接前导序列1(SL1),从而证实,在迄今为止研究的丝虫寄生虫中,只有匐行恶丝虫显示出独特的SL1序列。这里开发的PCR检测方法以及对5S核糖体间隔区的分析,可以进一步改善这些丝虫种类的流行病学和分子分析。