Larsen Nadja, Nissen Peter, Willats William G T
Food Microbiology, Department of Food Science (IFV), The Royal Veterinary and Agricultural University (KVL), Rolighedsvej 30, 1958 Frederiksberg C, Denmark.
Int J Food Microbiol. 2007 Feb 28;114(1):113-9. doi: 10.1016/j.ijfoodmicro.2006.10.033. Epub 2007 Jan 17.
The adhesion abilities of 11 strains of Lactobacillus were determined in vitro using the IPEC-J2 cell line as a model system. Bacteria cultures included the probiotic strains L. rhamnosus GG, L. reuteri ATCC 55730, L. johnsonii NCC 533 and L. reuteri DSM 12246, and new isolates of Lactobacillus ssp. Adhesion was quantified by scintillation counting of radiolabelled bound bacteria. The highest adhesion of 38%, was determined for L. reuteri DSM 12246 followed by L. plantarum Q47 with an adhesion level of 24%. Other strains showed moderate to low binding of less than 16%. Competitive adhesion experiments on IPEC-J2 cells demonstrated that strongly adhesive strains, as L. reuteri DSM 12246 and L. plantarum Q47, significantly reduced the attachment of the less adhesive strains, such as L. rhamnosus GG and L. johnsonii NCC 533, both under condition of co-incubation and in displacement assays, indicating that bacteria may share the same binding sites for attachment to intestinal cells. Furthermore, it was revealed that calcium ions significantly increased the binding of tested lactobacilli to IPEC-J2 cells; and therefore, added calcium may be useful in enhancing the adhesion of normally weakly adhesive probiotic cultures. In contrast, no significant change in adhesion of lactobacilli was observed in the presence of Mg and Zn ions. Displacement assays performed with pathogenic E. coli O138 showed that all tested Lactobacillus strains reduced the attachment of E. coli O138 to IPEC-J2 by more than 2-fold both in the presence and the absence of calcium ions. The strains of Lactobacillus did not differ significantly in the extent of their inhibition of E. coli O138 adhesion, indicating that the reduced adhesion of E. coli O138 was due to steric hindrance of the binding sites rather than to specific interactions.
以IPEC-J2细胞系作为模型系统,在体外测定了11株乳酸菌的黏附能力。细菌培养物包括益生菌菌株鼠李糖乳杆菌GG、罗伊氏乳杆菌ATCC 55730、约氏乳杆菌NCC 533和罗伊氏乳杆菌DSM 12246,以及乳酸菌属的新分离株。通过对放射性标记的结合细菌进行闪烁计数来定量黏附。罗伊氏乳杆菌DSM 12246的黏附率最高,为38%,其次是植物乳杆菌Q47,黏附水平为24%。其他菌株的结合率为中等至低水平,低于16%。在IPEC-J2细胞上进行的竞争性黏附实验表明,强黏附菌株,如罗伊氏乳杆菌DSM 12246和植物乳杆菌Q47,在共孵育条件下和置换试验中,均显著降低了弱黏附菌株,如鼠李糖乳杆菌GG和约氏乳杆菌NCC 533的黏附,这表明细菌可能共享相同的肠道细胞黏附结合位点。此外,研究发现钙离子显著增加了受试乳酸菌与IPEC-J2细胞的结合;因此,添加钙可能有助于增强通常弱黏附的益生菌培养物的黏附。相比之下,在镁离子和锌离子存在的情况下,未观察到乳酸菌黏附的显著变化。用致病性大肠杆菌O138进行的置换试验表明,在有钙离子和无钙离子的情况下,所有受试乳酸菌菌株均使大肠杆菌O138对IPEC-J2的黏附减少了2倍以上。乳酸菌菌株对大肠杆菌O138黏附的抑制程度没有显著差异,这表明大肠杆菌O138黏附减少是由于结合位点的空间位阻,而不是由于特异性相互作用。