AI Article Synopsis

  • Recent advancements in next-generation sequencing have revealed that many human infections, like chronic wounds and cystic fibrosis, often involve multiple microorganisms, also known as polymicrobial infections.
  • Polymicrobial infections are linked to higher treatment failures and poorer patient outcomes, yet standard clinical tests assess antimicrobial susceptibility using only single microbial samples.
  • The review emphasizes the need for new methods to evaluate antimicrobial susceptibility in polymicrobial contexts, as interactions between different microorganisms can alter their resistance and tolerance to treatments, ultimately affecting patient care.

Article Abstract

With the development of next generation sequencing technologies in recent years, it has been demonstrated that many human infectious processes, including chronic wounds, cystic fibrosis, and otitis media, are associated with a polymicrobial burden. Research has also demonstrated that polymicrobial infections tend to be associated with treatment failure and worse patient prognoses. Despite the importance of the polymicrobial nature of many infection states, the current clinical standard for determining antimicrobial susceptibility in the clinical laboratory is exclusively performed on unimicrobial suspensions. There is a growing body of research demonstrating that microorganisms in a polymicrobial environment can synergize their activities associated with a variety of outcomes, including changes to their antimicrobial susceptibility through both resistance and tolerance mechanisms. This review highlights the current body of work describing polymicrobial synergism, both inter- and intra-kingdom, impacting antimicrobial susceptibility. Given the importance of polymicrobial synergism in the clinical environment, a new system of determining antimicrobial susceptibility from polymicrobial infections may significantly impact patient treatment and outcomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912749PMC
http://dx.doi.org/10.3390/pathogens10020144DOI Listing

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