Interdepartmental Microbiology Graduate Program, Iowa State University, Ames, Iowa, USA.
Department of Food Science and Human Nutrition, Iowa State University, Ames, Iowa, USA.
Appl Environ Microbiol. 2024 Oct 23;90(10):e0148024. doi: 10.1128/aem.01480-24. Epub 2024 Oct 3.
Humans use dietary supplements for several intended effects, such as supplementing malnutrition. While these compounds have been developed for host end benefits, their ancillary impact on the gut microbiota remains unclear. The human gut has been proposed as a reservoir for the prevalent lateral transfer of antimicrobial resistance and virulence genes in bacteria through plasmid conjugation. Here, we studied the effect of dietary zinc supplements on the incidence of plasmid conjugation . Supplement effects were analyzed through standardized broth conjugation assays. The avian pathogenic (APEC) strain APEC-O2-211 was a donor of the multidrug resistance plasmid pAPEC-O2-211A-ColV, and the human commensal isolate HS-4 was the plasmid-free recipient. Bacterial strains were standardized and mixed 1:1 and supplemented 1:10 with water, or zinc derived from either commercial zinc supplements or zinc gluconate reagent at varying concentrations. We observed a significant reduction in donors, recipients, and transconjugant populations in conjugations supplemented with zinc, with a dose-dependent relationship. Additionally, we observed a significant reduction ( < 0.05) in log conjugation efficiency in zinc-treated reactions. Upregulation of the mRNA for the plasmid replication initiation gene and the subset of transfer genes , , , , , , , , , , , , , , and was observed. Furthermore, we observed a downregulation of the conjugal propilin gene and the entry exclusion gene . This study demonstrates the effect of dietary zinc supplements on the conjugal transfer of a multidrug resistance plasmid between pathogenic and commensal bacteria during conditions.IMPORTANCEThis study identifies dietary zinc supplementation as a potential novel intervention for mitigating the emergence of multidrug resistance in bacteria, thus preventing antibiotic treatment failure and death in patients and animals. Further studies are required to determine the applicability of this approach in an model.
人类使用膳食补充剂来达到多种预期效果,例如补充营养不良。虽然这些化合物是为宿主带来益处而开发的,但它们对肠道微生物群的辅助影响尚不清楚。人类肠道被认为是细菌中抗生素耐药性和毒力基因普遍横向转移的储库,通过质粒接合实现。在这里,我们研究了膳食锌补充剂对质粒接合发生率的影响。通过标准化肉汤接合测定来分析补充剂的效果。禽致病性大肠杆菌(APEC)菌株 APEC-O2-211 是多药耐药质粒 pAPEC-O2-211A-ColV 的供体,而人类共生分离株 HS-4 是无质粒的受体。将细菌菌株标准化并以 1:1 的比例混合,并以水或来自商业锌补充剂或葡萄糖酸锌试剂的锌以不同浓度 1:10 的比例进行补充。我们观察到添加锌后供体、受体和转导体的数量显著减少,且存在剂量依赖性关系。此外,我们还观察到锌处理反应中的接合效率对数显著降低(<0.05)。观察到质粒复制起始基因 和转移基因子集 、 、 、 、 、 、 、 、 、 、 、 、 和 的 mRNA 上调。此外,还观察到共轭前导基因 和进入排斥基因 的下调。这项研究表明,在 条件下,膳食锌补充剂会影响致病性和共生菌之间多药耐药质粒的接合转移。因此,该研究为预防患者和动物的抗生素治疗失败和死亡提供了一种潜在的新型干预措施。需要进一步的研究来确定这种方法在 模型中的适用性。