The intestinal colonization of Lactiplantibacillus plantarum AR113 is influenced by its mucins and intestinal environment

Abstract

Lactiplantibacillus plantarum is an important member of the probiotic family and colonization of the host intestinal is essential for its continued probiotic function. The mechanism of L. plantarum intestinal colonization has not been elucidated until now, an important reason being that the colonization process is influenced by a number of factors. In this study, to confirm the influences of adhesion ability and host intestinal environment on L. plantarum intestinal colonization, knockouts of L. plantarum AR113 mucin genes were constructed using CRISPR/Cas9 gene editing technology, and polyethylene glycol was used to reduce the intestinal flora abundance. The knockout of L. plantarum AR113 mucin genes barely altered the strain’s tolerance to acid and bile salts. Notably, the adhesion number of AR113ΔLp_1431ΔLp_2233ΔLp_2792 to HT-29 cells was reduced from 175 to 114 per 100 cells. Through in vivo colonization experiments, an increase in the fluorescence intensity of AR113 and AR113ΔLp_1431&2233&2792 was detected the day after the mice were fed, while the deletion of Lp_1431, Lp_2233 and Lp_2792 genes reduced the intestinal tract colonization time from 14 to 11 days. Both AR113 and AR113ΔLp_1431ΔLp_2233ΔLp_2792 were reproduced in the intestine by labeling with 5-(6)-carboxyfluorescein diacetate N-succinimidyl ester. The results showed that the change in fluorescence intensity was closely dependent on the number of adhesions. Finally, compared to the control group, the prolonged intestinal colonization time of AR113ΔLp_1431ΔLp_2233ΔLp_2792 increased mice intestinal flora abundance, with distributions in the duodenum, jejunum, ileum and colon. Collectively, both the intestinal environment and the adhesion ability of L. plantarum AR113 affected intestinal colonization, and the host’s intestinal genetic background may be a key factor in the intestinal colonization of L. plantarum.