Use of green fluorescent protein to tag lactic acid bacterium strains under development as live vaccine vectors

被引:99
作者
Geoffroy, MC
Guyard, C
Quatannens, B
Pavan, S
Lange, M
Mercenier, A
机构
[1] Inst Pasteur, Dept Microbiol Ecosyst, F-59019 Lille, France
[2] Inst Biol, UMR 3586, F-59019 Lille, France
关键词
D O I
10.1128/AEM.66.1.383-391.2000
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
The lactic acid bacteria (LAB) are safe microorganisms which are mainly used for the preparation of fermented foods and for probiotic applications, The potential of LAB as live vehicles for the production and delivery of therapeutic molecules such as antigens is also being actively investigated today. However, very little is known about the fate of live LAB when administered in vivo and about the interaction of these microorganisms with the nasal or gastrointestinal ecosystem, For future applications, it is essential to be able to discriminate the biotherapeutic strain from the endogenous microflora and to unravel the mechanisms underlying the postulated health-beneficial effect. We therefore started to investigate both aspects in a mouse model with two LAB species presently under development as live vaccine vectors, i.e., Lactococcus lactis and Lactobacillus plantarum. We have constructed different expression vectors carrying the gfp (green fluorescent protein [GFP]) gene from the jellyfish Aequoria victoria, and we found that this visible marker was best expressed when placed under the control of the inducible strong nisA promoter from L. lactis. Notably, a threshold amount of GFP was necessary to obtain a bright fluorescent phenotype. We further demonstrated that fluorescent L, plantarum NCIMB8826 can be enumerated and sorted by flow cytometry. Moreover, tagging of this strain with GFP allowed us to visualize its phagocytosis by macrophages in vitro and ex vivo and to trace it in the gastrointestinal tract of mice upon oral administration.
引用
收藏
页码:383 / 391
页数:9
相关论文
共 38 条
  • [1] CONSTRUCTION OF PLASMID VECTORS FOR THE DETECTION OF STREPTOCOCCAL PROMOTERS
    ACHEN, MG
    DAVIDSON, BE
    HILLIER, AJ
    [J]. GENE, 1986, 45 (01) : 45 - 49
  • [2] ON THE SAFETY OF LACTIC-ACID BACTERIA FROM FOOD
    ADAMS, MR
    MARTEAU, P
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1995, 27 (2-3) : 263 - 264
  • [3] Green fluorescent protein as a marker for Pseudomonas spp.
    Bloemberg, GV
    OToole, GA
    Lugtenberg, BJJ
    Kolter, R
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (11) : 4543 - 4551
  • [4] ANALYSIS OF GENE-CONTROL SIGNALS BY DNA-FUSION AND CLONING IN ESCHERICHIA-COLI
    CASADABAN, MJ
    COHEN, SN
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1980, 138 (02) : 179 - 207
  • [5] GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION
    CHALFIE, M
    TU, Y
    EUSKIRCHEN, G
    WARD, WW
    PRASHER, DC
    [J]. SCIENCE, 1994, 263 (5148) : 802 - 805
  • [6] Corthier G, 1999, BIOTHERAPEUTIC AGENTS AND INFECTIOUS DISEASES, P269
  • [7] Corthier G, 1998, APPL ENVIRON MICROB, V64, P2721
  • [8] Improved green fluorescent protein by molecular evolution using DNA shuffling
    Crameri, A
    Whitehorn, EA
    Tate, E
    Stemmer, WPC
    [J]. NATURE BIOTECHNOLOGY, 1996, 14 (03) : 315 - 319
  • [9] Functional analysis of promoters in the nisin gene cluster of Lactococcus lactis
    deRuyter, PGGA
    Kuipers, OP
    Beerthuyzen, MM
    vanAlenBoerrigter, I
    deVos, WM
    [J]. JOURNAL OF BACTERIOLOGY, 1996, 178 (12) : 3434 - 3439
  • [10] Controlled gene expression systems for Lactococcus lactis with the food-grade inducer nisin
    deRuyter, PGGA
    Kuipers, OP
    deVos, WM
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) : 3662 - 3667