IS901, A NEW MEMBER OF A WIDESPREAD CLASS OF ATYPICAL INSERTION SEQUENCES, IS ASSOCIATED WITH PATHOGENICITY IN MYCOBACTERIUM-AVIUM

被引:151
作者
KUNZE, ZM
WALL, S
APPELBERG, R
SILVA, MT
PORTAELS, F
MCFADDEN, JJ
机构
[1] UNIV SURREY, SCH BIOL SCI, MOLEC MICROBIOL GRP, GUILDFORD GU2 5XH, SURREY, ENGLAND
[2] UNIV PORTO, CTR CYTOL EXPTL, OPORTO, PORTUGAL
[3] INST TROP MED, ANTWERP, BELGIUM
关键词
D O I
10.1111/j.1365-2958.1991.tb02157.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An insertion sequence (IS901), found in pathogenic strains of Mycobacterium avium, but absent in M. avium complex isolates from patients with acquired immune deficiency syndrome (AIDS), has been isolated and sequenced. This insertion element has a nucleotide sequence of 1472 bp, with one open reading frame (ORF1), which codes for a protein of 401 amino acids. The amino acid sequence, terminal ends and target site of IS901 are similar to those of IS900, present in Mycobacterium paratuberculosis. However, the DNA sequences of these two IS elements exhibit only 60% homology, compared to a DNA homology of 98% between their respective hosts. IS901, like IS900, appears to belong to a family of related insertion elements present in actinomycetes and other bacteria. M. avium strains containing IS901 were found to be more virulent in mice than closely related strains lacking IS901. IS901 may be a useful tool for the study of the genetics of virulence in the M. avium complex and for obtaining stable integration of foreign genes into mycobacteria.
引用
收藏
页码:2265 / 2272
页数:8
相关论文
共 30 条
[21]   CROHNS DISEASE-ISOLATED MYCOBACTERIA ARE IDENTICAL TO MYCOBACTERIUM-PARATUBERCULOSIS, AS DETERMINED BY DNA PROBES THAT DISTINGUISH BETWEEN MYCOBACTERIAL SPECIES [J].
MCFADDEN, JJ ;
BUTCHER, PD ;
CHIODINI, R ;
HERMONTAYLOR, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (05) :796-801
[22]   THE USE OF DNA PROBES IDENTIFYING RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS TO EXAMINE THE MYCOBACTERIUM-AVIUM COMPLEX [J].
MCFADDEN, JJ ;
BUTCHER, PD ;
THOMPSON, J ;
CHIODINI, R ;
HERMONTAYLOR, J .
MOLECULAR MICROBIOLOGY, 1987, 1 (03) :283-291
[23]  
MURPHY E, 1988, TRANSPOSITION, P59
[24]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[25]  
SNIDER DE, 1987, AM REV RESPIR DIS, V136, P492
[26]   DETECTION OF SPECIFIC SEQUENCES AMONG DNA FRAGMENTS SEPARATED BY GEL-ELECTROPHORESIS [J].
SOUTHERN, EM .
JOURNAL OF MOLECULAR BIOLOGY, 1975, 98 (03) :503-+
[27]   USE OF HIGHLY SPECIFIC DNA PROBES AND THE POLYMERASE CHAIN-REACTION TO DETECT MYCOBACTERIUM-PARATUBERCULOSIS IN JOHNES DISEASE [J].
VARY, PH ;
ANDERSEN, PR ;
GREEN, E ;
HERMONTAYLOR, J ;
MCFADDEN, JJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (05) :933-937
[28]   SIMPLE ENZYMIC METHOD FOR ISOLATION OF DNA FROM DIVERSE BACTERIA [J].
VISUVANATHAN, S ;
MOSS, MT ;
STANFORD, JL ;
HERMONTAYLOR, J ;
MCFADDEN, JJ .
JOURNAL OF MICROBIOLOGICAL METHODS, 1989, 10 (02) :59-64
[29]  
YUE X, 1988, MOL BIOL EVOL, V5, P675
[30]   DOUBLE-STRANDED DNA SEQUENCING AS A CHOICE FOR DNA SEQUENCING [J].
ZHANG, H ;
SCHOLL, R ;
BROWSE, J ;
SOMERVILLE, C .
NUCLEIC ACIDS RESEARCH, 1988, 16 (03) :1220-1220