St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.
Arietis Pharma, 650 Albany Street, Suite 114, Boston, MA 02118, USA.
Curr Opin Microbiol. 2022 Dec;70:102203. doi: 10.1016/j.mib.2022.102203. Epub 2022 Sep 23.
Helicobacter pylori is an important human pathogen with increasing antimicrobial resistance to standard-of-care antibiotics. Treatment generally includes a combination of classical broad-spectrum antibiotics and a proton-pump inhibitor, which often leads to perturbation of the gut microbiome and the potential for the development of antibiotic resistance. In this review, we examine reports, primarily from the past decade, on the discovery of new anti-H. pylori therapeutics, including approaches to develop narrow-spectrum and mechanistically unique antibiotics to treat these infections in their gastric niche. Compound series that target urease, respiratory complex I, and menaquinone biosynthesis are discussed in this context, along with bivalent antibiotic approaches that suppress resistance development. With increases in the understanding of the unique physiology of H. pylori and technological advances in the field of antibacterial drug discovery, there is a clear promise that novel therapeutics can be developed to effectively treat H. pylori infections.
幽门螺杆菌是一种重要的人类病原体,其对抗生素的耐药性不断增加。治疗通常包括经典广谱抗生素和质子泵抑制剂的联合使用,这往往会导致肠道微生物组的紊乱和抗生素耐药性的发展。在这篇综述中,我们检查了主要来自过去十年的关于发现新的抗幽门螺杆菌治疗方法的报告,包括开发针对这些在胃内定植部位感染的窄谱和机制独特抗生素的方法。本文讨论了针对尿素酶、呼吸复合物 I 和甲萘醌生物合成的化合物系列,以及抑制耐药性发展的双价抗生素方法。随着对幽门螺杆菌独特生理学的理解的增加和抗菌药物发现领域的技术进步,显然有希望开发出新的疗法来有效治疗幽门螺杆菌感染。