Construction of D29 shuttle phasmids and luciferase reporter phages for detection of mycobacteria

Robert E. Pearson, Stewart Jurgensen, Gary J. Sarkis, Graham F. Hatfull, William R. Jacobs

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

Diseases caused by Mycobacterium tuberculosis, M. leprae and M. avium, cause significant morbidity and mortality worldwide. Effective treatments require that the organisms be speciated and that drug susceptibilities for the causative organisms be characterized. Reporter phage technology has been developed as a rapid and convenient method for identifying mycobacterial species and evaluating drug resistance. In this report we describe the construction of luciferase reporter phages from mycobacterio-phage D29 DNA. Shuttle phasmids were first constructed with D29 in order to identify non-essential regions of the D29 genomes and to introduce unique cloning sites within that region. Using this approach, we observed that all of the D29 shuttle phasmids had the cosmid vector localized to one area of the phage genome near one cohesive end. These shuttle phasmids had been constructed with a cosmid that could be readily excised from the D29 genome with different sets of restriction enzymes. Luciferase reporter phages were made by substituting the luciferase cassette for the cosmid vector. Recombinant phages with the luciferase cassette fall into two groups. One group produced light and had the expression cassette oriented with the promoter directing transcription away from the cohesive end. In contrast, the other group had the expression cassette in the opposite orientation and failed to produce light during lytic infection, but did produce light in L5 lysogens which are known to repress D29 promoters. These results suggest that a phage promoter of the D29 phage can occlude the expression of a promoter introduced into this region. D29 luciferase reporter phages are capable of detecting low numbers of L5 lysogens like L5 luciferase phages. However, unlike L5 luciferase phages, D29 luciferase phages can readily infect M. tuberculosis and M. bovis BCG, demonstrating that these phages can be used to evaluate drug susceptibilities of many types of mycobacteria.

Original languageEnglish (US)
Pages (from-to)129-136
Number of pages8
JournalGene
Volume183
Issue number1-2
DOIs
StatePublished - Dec 1 1996

Fingerprint

Mycobacterium
Luciferases
Bacteriophages
Cosmids
Genome
Mycobacterium tuberculosis
Light
Mycobacterium bovis
Drug Resistance
Pharmaceutical Preparations
Organism Cloning

Keywords

  • Cosmids
  • Luciferase
  • Mycobacteriophages
  • Non-essential regions
  • Phage immunity
  • Tuberculosis

ASJC Scopus subject areas

  • Genetics

Cite this

Construction of D29 shuttle phasmids and luciferase reporter phages for detection of mycobacteria. / Pearson, Robert E.; Jurgensen, Stewart; Sarkis, Gary J.; Hatfull, Graham F.; Jacobs, William R.

In: Gene, Vol. 183, No. 1-2, 01.12.1996, p. 129-136.

Research output: Contribution to journalArticle

Pearson, Robert E. ; Jurgensen, Stewart ; Sarkis, Gary J. ; Hatfull, Graham F. ; Jacobs, William R. / Construction of D29 shuttle phasmids and luciferase reporter phages for detection of mycobacteria. In: Gene. 1996 ; Vol. 183, No. 1-2. pp. 129-136.
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