Gene transfer from engineered Lactococcus lactis strains to Enterococcus faecalis in the digestive tract of gnotobiotic mice.

M Gruzza, P Langella, Y Duval-Iflah, R Ducluzeau
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Abstract

The introduction of genetically modified organisms into food products requires an evaluation of the behaviour and the dissemination of foreign genes of such organisms among the human intestinal microflora. The conjugal transfer, both in vitro and in vivo (in mice digestive tract) of DNA from Lactococcus lactis donor strains to an Enterococcus faecalis strain isolated from human faecal flora was studied. We followed the transfer of (1) the self-transmissible plasmid pIL205; (2) two non-self-transmissible but mobilizable plasmids, pIL252 and pIL253; (3) one plasmid, pMS1.5B, integrated into the chromosome of L. lactis. In vitro, the transfer frequency of pIL205 (expressed as the number of transconjugants per donor cell) was 9.6 x 10(-4); mobilization of one of the non-self-transmissible plasmids, pIL253, was observed (4.9 x 10(-7)). In vivo, only transfer of pIL205 and pIL253 occurred, but the frequency was not determined. The transfer of pMS1.5B was not detected in vitro or in vivo.

转基因乳酸乳球菌向粪肠球菌的基因转移。
将转基因生物引入食品中需要对这种生物的行为和外源基因在人类肠道菌群中的传播进行评估。研究了乳酸乳球菌供体DNA在体外和体内(小鼠消化道)向从人类粪便菌群中分离的粪肠球菌菌株的结合转移。我们观察了(1)自传质粒pIL205的转移;(2)两个非自传但可动员的质粒,pIL252和pIL253;(3) 1个质粒pMS1.5B整合到乳杆菌的染色体上。在体外,pIL205的转移频率(以每个供体细胞的转偶联数表示)为9.6 x 10(-4);观察到其中一个非自传质粒pIL253的动员(4.9 x 10(-7))。在体内,只发生了pIL205和pIL253的转移,但频率尚未确定。体外和体内均未检测到pMS1.5B的转移。
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