4.7 Article

Fosfomycin Resistance Evolutionary Pathways of Stenotrophomonas maltophilia in Different Growing Conditions

Journal

Publisher

MDPI
DOI: 10.3390/ijms23031132

Keywords

Stenotrophomonas maltophilia; experimental evolution; fosfomycin resistance

Funding

  1. Instituto de Salud Carlos III-European Development Regional Fund A Way to Achieve Europe [RD16/0016/0011]
  2. Comunidad de Madrid (Spain) [S2017/BMD-3691 InGEMICS-CM]
  3. European Structural and Investment Funds
  4. FPI fellowship from MINECO
  5. [MCIN/AEI/10.13039/501100011033 (PID2020-113521RB-I00)]

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The rise of multidrug-resistant Gram-negative pathogens and the lack of novel antibiotics has led to the reutilization of old antibiotics, such as fosfomycin. Stenotrophomonas maltophilia is a Gram-negative, non-fermenter opportunistic pathogen with low susceptibility to antibiotics. Fosfomycin resistance in S. maltophilia is caused by the inactivation of enzymes in its central carbon metabolism, linking metabolism with antibiotic resistance. Different growing conditions can impact the pathways of fosfomycin resistance evolution in S. maltophilia.
The rise of multidrug-resistant Gram-negative pathogens and the lack of novel antibiotics to address this problem has led to the rescue of old antibiotics without a relevant use, such as fosfomycin. Stenotrophomonas maltophilia is a Gram-negative, non-fermenter opportunistic pathogen that presents a characteristic low susceptibility to several antibiotics of common use. Previous work has shown that while the so-far described mechanisms of fosfomycin resistance in most bacteria consist of the inactivation of the target or the transporters of this antibiotic, as well as the production of antibiotic-inactivating enzymes, these mechanisms are not selected in S. maltophilia fosfomycin-resistant mutants. In this microorganism, fosfomycin resistance is caused by the inactivation of enzymes belonging to its central carbon metabolism, hence linking metabolism with antibiotic resistance. Consequently, it is relevant to determine how different growing conditions, including urine and synthetic sputum medium that resemble infection, could impact the evolutionary pathways towards fosfomycin resistance in S. maltophilia. Our results show that S. maltophilia is able to acquire high-level fosfomycin resistance under all tested conditions. However, although some of the genetic changes leading to resistance are common, there are specific mutations that are selected under each of the tested conditions. These results indicate that the pathways of S. maltophilia evolution can vary depending on the infection point and provide information for understanding in more detail the routes of fosfomycin resistance evolution in S. maltophilia.

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