Hamed Selwan, Emara Mohamed, Tohidifar Payman, Rao Christopher V
Department of Microbiology and Immunology, Faculty of Pharmacy, Helwan University- Ain Helwan, Helwan, Cairo, Egypt.
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
PLoS One. 2025 Jan 7;20(1):e0313508. doi: 10.1371/journal.pone.0313508. eCollection 2025.
Salmonella enterica is a common foodborne pathogen that causes intestinal illness varying from mild gastroenteritis to life-threatening systemic infections. The frequency of outbreaks due to multidrug-resistant Salmonella has been increased in the past few years with increasing numbers of annual deaths. Therefore, new strategies to control the spread of antimicrobial resistance are required. In this work, we found that N-acetyl cysteine (NAC) inhibits S. enterica at MIC of 3 mg ml-1 and synergistically activates the bactericidal activities of common antibiotics from three-fold for ampicillin and apramycin up to1000-fold for gentamycin. In addition, NAC inhibits the expression of virulence genes at sub-inhibitory concentrations in a dose-dependent manner. The whole-genome sequencing revealed that continuous exposure of S. enterica to NAC leads to the development of resistance; these resistant strains are attenuated for virulence. These results suggest that NAC may be a promising adjuvant to antibiotics for treating S. enterica in combination with other antibiotics.
肠炎沙门氏菌是一种常见的食源性病原体,可引起从轻度肠胃炎到危及生命的全身感染等不同程度的肠道疾病。在过去几年中,由于多重耐药性沙门氏菌导致的疫情爆发频率不断增加,每年死亡人数也在上升。因此,需要新的策略来控制抗菌药物耐药性的传播。在这项研究中,我们发现N-乙酰半胱氨酸(NAC)在3 mg/ml的最低抑菌浓度下可抑制肠炎沙门氏菌,并协同激活常用抗生素的杀菌活性,对氨苄青霉素和阿普拉霉素的增效倍数为3倍,对庆大霉素的增效倍数高达1000倍。此外,NAC在亚抑菌浓度下以剂量依赖的方式抑制毒力基因的表达。全基因组测序显示,肠炎沙门氏菌持续暴露于NAC会导致耐药性的产生;这些耐药菌株的毒力减弱。这些结果表明,NAC可能是一种有前景的抗生素佐剂,可与其他抗生素联合用于治疗肠炎沙门氏菌感染。