5S ribosomal RNA gene repeat sequences define at least eight groups of plant trypanosomatids (Phytomonas spp.):: Phloem-restricted pathogens form a distinct section

被引:25
作者
Dollet, M
Sturm, NR
Sánchez-Moreno, M
Campbell, DA
机构
[1] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[2] Univ Granada, Fac Ciencias, Grp Bioquim & Parasitol Mol, Inst Biotechnol, E-18017 Granada, Spain
[3] CIRAD, F-34398 Montpellier, France
关键词
coconut; genetic heterogeneity; insect trypanosomatids; kinetoplastid protozoa; molecular typing; oil palm; PCR; plant trypanosomatids;
D O I
10.1111/j.1550-7408.2000.tb00091.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Trypanosomatids isolated from plants have been assigned typically into the genus Phytomonas. Such designations do not reflect the biology of the diverse isolates; confusion may arise due to the transient presence in plants of monogenetic (insect) trypanosomatids deposited by phytophagous bugs. To develop further molecular markers for the plant kinetoplastids, we have obtained the DNA sequence of the 5S ribosomal RNA gene from 24 isolates harvested from phloem, latex, and fruit. Small, distinct sequence differences were found at the 3'-ends of the transcribed regions; substantial sequence and size differences were found in the non-transcribed regions. Alignment of the gene sequences from all the isolates suggested the presence of eight groupings. While six groups contained isolates from single plant tissues, groups C and A contained isolates from both fruit and latex. The DNA sequences of the 10 phloem-restricted pathogenic isolates from South America and the Carribean were highly conserved and thus comprised a single group (H). The conserved nature of the 5S ribosomal RNA genes in these plant pathogens supports the proposal that they be considered as a distinct section, the phloemicola.
引用
收藏
页码:569 / 574
页数:6
相关论文
共 25 条
[1]  
[Anonymous], LANCET
[2]   NUCLEOTIDE-SEQUENCES IN XENOPUS 5S DNA REQUIRED FOR TRANSCRIPTION TERMINATION [J].
BOGENHAGEN, DF ;
BROWN, DD .
CELL, 1981, 24 (01) :261-270
[3]  
Burstein ZA, 1956, ARCH PER PAT CLIN, V10, P1
[4]  
Campbell David A., 1997, Memorias do Instituto Oswaldo Cruz, V92, P12
[5]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[6]  
DOLLET M, 1977, CR ACAD SCI D NAT, V284, P643
[7]  
DOLLET M, 1994, IDENTIFICATION CHARA, P412
[8]   Biochemical characterisation of flagellates isolated from fruits and seeds from Brazil [J].
Fernández-Ramos, C ;
Luque, F ;
Fernández-Becerra, C ;
Osuna, A ;
Jankevicius, SI ;
Jankevicius, JV ;
Rosales, MJ ;
Sánchez-Moreno, M .
FEMS MICROBIOLOGY LETTERS, 1999, 170 (02) :343-348
[9]  
FernandezBecerra C, 1996, FEMS MICROBIOL LETT, V145, P463, DOI 10.1016/S0378-1097(96)00453-3
[10]   AN ISOENZYME ANALYSIS OF THE GENUS PHYTOMONAS - GENETIC, TAXONOMIC AND EPIDEMIOLOGIC SIGNIFICANCE [J].
GUERRINI, F ;
SEGUR, C ;
GARGANI, D ;
TIBAYRENC, M ;
DOLLET, M .
JOURNAL OF PROTOZOOLOGY, 1992, 39 (04) :516-521