PHAGE INFECTION, TRANSFECTION AND TRANSFORMATION OF MYCOBACTERIUM-AVIUM COMPLEX AND MYCOBACTERIUM-PARATUBERCULOSIS

被引:65
|
作者
FOLEYTHOMAS, EM
WHIPPLE, DL
BERMUDEZ, LE
BARLETTA, RG
机构
[1] UNIV NEBRASKA, CTR BIOTECHNOL, DEPT VET & BIOMED SCI, LINCOLN, NE 68583 USA
[2] USDA, NATL ANIM DIS CTR, AMES, IA 50010 USA
[3] CALIF PACIFIC MED CTR, RES INST, KUZELL INST ARTHRIT & INFECT DIS, SAN FRANCISCO, CA 94115 USA
来源
MICROBIOLOGY-SGM | 1995年 / 141卷
关键词
MYCOBACTERIUM AVIUM COMPLEX; MYCOBACTERIUM PARATUBERCULOSIS; MYCOBACTERIOPHAGE; SHUTTLE VECTORS; TRANSFORMATION;
D O I
10.1099/13500872-141-5-1173
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mycobacterium avium complex strains and Mycobacterium paratuberculosis are closely related intracellular pathogens affecting humans and animals. M. avium complex infections are a leading cause of morbidity and mortality in AIDS patients, and M. paratuberculosis is the agent of Johne's disease in ruminants. Genetic manipulation of these micro-organisms would facilitate the understanding of their pathogenesis, the construction of attenuated vaccine strains and the development of new drugs and treatment methods. This paper describes the replication of mycobacterial shuttle phasmids and plasmids, and the expression of the firefly luciferase reporter gene in M. avium complex and M. paratuberculosis. The mycobacteriophage TM4 propagated on M. smegmatis or M. paratuberculosis plagued at the same efficiency on these two mycobacterial hosts. Screening of M. avium complex and M. paratuberculosis clinical isolates with TM4-derived luciferase reporter phages demonstrated that the majority of these isolates were susceptible to TM4. Conditions for introduction of DNA were determined by transfection of M. paratuberculosis with TM4 DNA and applied to isolate kanamycin-resistant transformants of M. avium complex and M. paratuberculosis with Escherichia coli-Mycobacterium shuttle plasmids. Recombinant plasmids were recovered from transformants without apparent loss of DNA sequences. These results provide the basis for the genetic manipulation of these pathogenic mycobacterial species.
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页码:1173 / 1181
页数:9
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