Use of a lux reporter system for monitoring rapid changes in α-toxin gene expression in Clostridium perfringens during growth
To determine whether the luxA– luxB reporter system is suitable as a sensitive reporter for rapid real-time measurements of α-toxin gene ( cpa) expression in Clostridium perfringens, and to widen the range of α-toxin-producing C. perfringens strains examined with respect to cpa expression during gro...
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Veröffentlicht in: | FEMS microbiology letters 2000-07, Vol.188 (1), p.29-33 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To determine whether the
luxA–
luxB reporter system is suitable as a sensitive reporter for rapid real-time measurements of α-toxin gene (
cpa) expression in
Clostridium perfringens, and to widen the range of α-toxin-producing
C. perfringens strains examined with respect to
cpa expression during growth, the reporter plasmid pPS14 (possessing the α-toxin promoter region plus 0.7 kb of upstream region linked to the
luxA–
luxB genes), was used in batch growth experiments of
C. perfringens P90.2.2, an α-toxin-producing strain with no known association with disease. Levels of in vivo bioluminescence obtained during growth were broadly in agreement with previous mRNA and reporter studies of
cpa expression (Bullifent et al., FEMS Microbiol. Lett. 131 (1995) 99–105), confirming the suitability of
lux as an accurate reporter system in this organism, but the sensitive nature of the
lux reporter permitted the in vivo detection of a very rapid reduction in expression during late-exponential phase that was not attributable to loss in cell viability or limiting bioluminescence assay substrates. There was also a small peak in
cpa expression in early- to mid-exponential phase cells, that was not detected in previous studies with other reporters. This may be indicative of the exquisite sensitivity of the
lux reporter, or this may be a difference in
cpa expression that occurs specifically in this
C. perfringens strain. Whichever is the case, these results confirm the complexity of α-toxin gene expression in different strains of this pathogenic bacterium. |
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ISSN: | 0378-1097 1574-6968 |
DOI: | 10.1016/S0378-1097(00)00208-1 |