The influence of green fluorescent protein incorporation on bacterial physiology: a note of caution

被引:33
作者
Allison, D. G. [1 ]
Sattenstall, M. A. [1 ]
机构
[1] Univ Manchester, Sch Pharm & Pharmaceut Sci, Manchester M13 9PL, Lancs, England
关键词
antimicrobial susceptibility; bacterial; physiology; cetrimide; ciprofloxacin; fitness; cost; GFP; tetracycline;
D O I
10.1111/j.1365-2672.2006.03243.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To investigate the effect of green flourescent protein (GFP) incorporation on bacterial physiology. Methods and Results: Comparisons were made between four different isogenic pairings of non-GFP-containing parents and their GFP-containing transformants with respect to growth rate and antimicrobial susceptibility. For the latter, sensitivities to 12 different antibiotics were measured initially by disc-diffusion assay, and then subsequently by generation of dose-dependent survival curves for I h exposure to different concentrations of tetracycline, ciprofloxacin and cetrimide USP. Whilst no significant difference in growth rate was observed, GFP-containing strains were uniformly and significantly more sensitive to all antimicrobial agents tested, excluding the beta-lactams, than their respective non-GFP-containing counterparts. Conclusions: GFP incorporation has a significant effect on bacterial physiology and can modulate antimicrobial susceptibility. Significance and Impact of the Study: Transformation with GFP can affect the physiology of bacterial cells. This may therefore affect the quality and accuracy of data generated depending on the application for which GFP is used.
引用
收藏
页码:318 / 324
页数:7
相关论文
共 20 条
[11]   Tn5393d, a complex Tn5393 derivative carrying the PER-1 extended-spectrum β-lactamase gene and other resistance determinants [J].
Mantengoli, E ;
Rossolini, GM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (08) :3289-3296
[12]  
Parry JD, 2001, FEMS MICROBIOL ECOL, V35, P11, DOI 10.1111/j.1574-6941.2001.tb00783.x
[13]   Physical linkage of Tn3 and part of Tn1721 in a tetracycline and ampicillin resistance plasmid from Salmonella Typhimurium [J].
Pasquali, F ;
Kehrenberg, C ;
Manfreda, G ;
Schwarz, S .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 55 (04) :562-565
[14]   Fitness cost of the green fluorescent protein in gastrointestinal bacteria [J].
Rang, C ;
Galen, JE ;
Kaper, JB ;
Chao, L .
CANADIAN JOURNAL OF MICROBIOLOGY, 2003, 49 (09) :531-537
[15]  
Rosochacki Stanislaw Jozef, 2002, Acta Microbiol Pol, V51, P205
[16]  
Sacchetti A, 2001, J CELL BIOCHEM, P117
[17]   Green fluorescent protein as a novel species-specific marker in enteric dual-species biofilms [J].
Skillman, LC ;
Sutherland, IW ;
Jones, MV ;
Goulsbra, A .
MICROBIOLOGY-SGM, 1998, 144 :2095-2101
[18]   Green fluorescent protein as a reporter for spatial and temporal gene expression in Streptomyces coelicolor A3(2) [J].
Sun, JH ;
Kelemen, GH ;
Fernández-Abalos, JM ;
Bibb, MJ .
MICROBIOLOGY-UK, 1999, 145 :2221-2227
[19]  
TAMARIN RH, 1996, PRINCIPLES GENETICS
[20]   The green fluorescent protein [J].
Tsien, RY .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :509-544