Sandoval-Mosqueda Ivonne Lizeth, Llorente-Bousquets Adriana, Soto Carlos, Márquez Crisóforo Mercado, Fadda Silvina, Del Río García Juan Carlos
Posgrado, Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de Mexico, km 2.5 Carretera Cuautitlán-Teoloyucan, San Sebastian Xhala, Cuautitlán Izcalli 54714, Mexico.
Ingeniería y Tecnología, Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, km 2.5 Carretera Cuautitlán-Teoloyucan, San Sebastian Xhala, Cuautitlán Izcalli 54714, Mexico.
Microorganisms. 2023 Apr 4;11(4):942. doi: 10.3390/microorganisms11040942.
Considering the objectives of "One Health" and the Sustainable development Goals "Good health and well-being" for the development of effective strategies to apply against bacterial resistance, food safety dangers, and zoonosis risks, this project explored the isolation and identification of strains from the intestinal tract of recently weaned mice; as well as the assessment of antibacterial activity against clinical and zoonotic pathogens. For molecular identification, 16S rRNA gene-specific primers were used and, via BLAST-NCBI, 16 , one and one strains were identified and registered in GenBank after the confirmation of their identity percentage and the phylogenetic analysis of the 16 strains and their association with . The 18 isolated strains showed antibacterial activity during agar diffusion tests against ATCC 15313, enteropathogenic O103, and ATCC 49943. Electrophoretic and zymographic techniques confirmed the presence of bacteriolytic bands with a relative molecular mass of 107 kDa and another of 24 kDa in strains. UPLC-MS analysis allowed the identification of a 107 kDa lytic protein as an N-acetylmuramoyl-L-amidase involved in cytolysis and considered a bacteriolytic enzyme with antimicrobial activity. The 24 kDa band displayed similarity with a portion of protein with aminopeptidase function. It is expected that these findings will impact the search for new strains and their metabolites with antibacterial activity as an alternative strategy to inhibit pathogens associated with major health risks that help your solution.
考虑到“同一健康”目标以及可持续发展目标“良好健康与福祉”,为制定应对细菌耐药性、食品安全风险和人畜共患病风险的有效策略,本项目探索了从刚断奶小鼠肠道中分离和鉴定菌株;以及评估其对临床和人畜共患病病原体的抗菌活性。对于分子鉴定,使用了16S rRNA基因特异性引物,并通过BLAST-NCBI,在确认其身份百分比以及对16株菌株进行系统发育分析及其与……的关联后,鉴定出16株、1株和1株菌株并在GenBank中注册。在琼脂扩散试验中,18株分离菌株对金黄色葡萄球菌ATCC 15313、肠致病性大肠杆菌O103和单核细胞增生李斯特菌ATCC 49943显示出抗菌活性。电泳和酶谱技术证实了在……菌株中存在相对分子质量为107 kDa和另一条24 kDa的溶菌带。超高效液相色谱-质谱联用分析鉴定出一种107 kDa的溶菌蛋白为参与细胞溶解的N-乙酰胞壁酰-L-丙氨酸酰胺酶,并被认为是一种具有抗菌活性的溶菌酶。24 kDa的条带与具有氨肽酶功能的部分蛋白质显示出相似性。预计这些发现将影响对具有抗菌活性的新菌株及其代谢产物的寻找,作为抑制与主要健康风险相关病原体的替代策略,有助于解决问题。