Multiple polymorphic sites at the ITS and ATAN loci in cultured isolates of Perkinsus marinus

被引:32
作者
Brown, GD [1 ]
Hudson, KL [1 ]
Reece, KS [1 ]
机构
[1] Virginia Inst Marine Sci, Coll William & Mary, Gloucester Point, VA 23062 USA
关键词
internal transcribed spacer 1; internal transcribed spacer 2. 5.8S rRNA gene; polymorphism;
D O I
10.1111/j.1550-7408.2004.tb00572.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sequence analysis of genomic DNA from the protozoan parasite Perkinsus marinas at two loci revealed genetic polymorphisms within and among different cultured isolates. Genomic DNA from 12 Perkinsus marinas isolates was amplified at the internal transcribed spacer region and at an anonymous locus previously identified to contain polymorphisms by restriction fragment length polymorphism analysis. Fourteen polymorphic nucleotide positions were identified at the internal transcribed spacer region; eight in internal transcribed spacer I and six in internal transcribed spacer 2. Thirteen polymorphic nucleotide sites were identified within the anonymous locus. In some instances, more than three different sequences were observed at both the internal transcribed spacer region and at the anonymous locus from a single clonal isolate, suggesting the possibility of recombination in cultured cells and/or strand jumping during the polymerase chain reaction. Intra-isolate sequence variation (3.46% for the anonymous locus and 3.08% for internal transcribed spacer 1) was in several cases as high as inter-isolate sequence variation, even in one isolate where recombination was not evident. High intra- and inter-isolate variation detected at both loci demonstrates the importance of determining the genetic variation of each locus prior to development of sequence-based molecular diagnostics.
引用
收藏
页码:312 / 320
页数:9
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