Animal & Plant Sciences, University of Sheffield, Western Bank, Sheffield, United Kingdom ; Department of Entomology, Cornell University, Ithaca, New York, United States of America.
PLoS One. 2013 Oct 18;8(10):e76521. doi: 10.1371/journal.pone.0076521. eCollection 2013.
With a diminishing number of effective antibiotics, there has been interest in developing antimicrobial peptides (AMPs) as drugs. However, any new drug faces potential bacterial resistance evolution. Here, we experimentally compare resistance evolution in Staphylococcus aureus selected by three AMPs (from mammals, amphibians and insects), a combination of two AMPs, and two antibiotics: the powerful last-resort vancomycin and the classic streptomycin. We find that resistance evolves readily against single AMPs and against streptomycin, with no detectable fitness cost. However the response to selection from our combination of AMPs led to extinction, in a fashion qualitatively similar to vancomycin. This is consistent with the hypothesis that simultaneous release of multiple AMPs during immune responses is a factor which constrains evolution of AMP resistant pathogens.
随着有效抗生素数量的减少,人们对开发抗菌肽 (AMPs) 作为药物产生了兴趣。然而,任何新药都面临着潜在的细菌耐药性进化的问题。在这里,我们通过实验比较了三种 AMPs(来自哺乳动物、两栖动物和昆虫)、两种 AMPs 组合以及两种抗生素(强大的最后手段万古霉素和经典的链霉素)选择的金黄色葡萄球菌的耐药性进化。我们发现,单一 AMPs 和链霉素的耐药性很容易进化,而且没有检测到明显的适应性成本。然而,我们的 AMP 组合的选择导致了灭绝,这与万古霉素的情况在性质上是相似的。这与以下假设一致,即在免疫反应中同时释放多种 AMP 是限制 AMP 耐药病原体进化的一个因素。