Mycoplasma pneumoniae P1 type 1-and type 2-specific sequences within the P1 cytadhesin gene of individual strains

被引:51
|
作者
Dorigo-Zetsma, JW
Wilbrink, B
Dankert, J
Zaat, SAJ
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
[2] Natl Inst Publ Hlth & Environm, Diagnost Lab Infect Dis & Perinatal Screening, NL-3720 BA Bilthoven, Netherlands
关键词
D O I
10.1128/IAI.69.9.5612-5618.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mycoplasma pneumoniae strains traditionally are divided into two types, based on sequence variation in the P1 gene. Recently, however, we have identified 8 P1 subtypes by restriction fragment length polymorphism analysis. In the present study the P1 gene sequences of three P1 type I and two P1 type 2 M. pneumoniae strains were analyzed. A new P1 gene sequence in a type 1 strain with partial similarity to a recently reported variable region in the P1 gene of an M. pneumoniae type 2 strain (T. Kenri, R. Taniguchi, Y. Sasaki, N. Okazaki, M. Narita, K. Izumikawa, M. Umetsu, and T.Sasaki, Infect. Immun. 67:4557-4562, 1999) was identified. In addition, the P1 gene of the type I strain contained another region with nucleotide polymorphisms identical to a stretch in the PI gene of one of our type 2 strains. These findings indicate that recombination between sequences specific for P1 type I and type 2 had occurred and that P1 type I and type 2 hybrid sequences can be present within the P1 gene of an individual strain. Identical or nearly identical variable PI gene sequences were present in several repetitive regions outside the PI gene locus in the genome of M. pneumoniae strain M129, implying recombination as a mechanism for generation of the P1 gene variation. Additionally, in the P1 gene sequences of four of the five strains studied, single-nucleotide polymorphisms different from the previously reported PI type 1 and 2 characteristic sequences were identified. The polymorphic sites are candidate targets for genotyping of M. pneumoniae by direct sequencing of amplicons from clinical specimens.
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页码:5612 / 5618
页数:7
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