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Use of epigenetically modified bacteriophage and dual beta-lactams to treat a Mycobacterium abscessus sternal wound infection

  • Madison Cristinziano
  • , Elena Shashkina
  • , Liang Chen
  • , Jaime Xiao
  • , Melissa B. Miller
  • , Christina Doligalski
  • , Raymond Coakley
  • , Leonard Jason Lobo
  • , Brent Footer
  • , Luther Bartelt
  • , Lawrence Abad
  • , Daniel A. Russell
  • , Rebecca Garlena
  • , Michael J. Lauer
  • , Maggie Viland
  • , Ari Kaganovsky
  • , Emily Mowry
  • , Deborah Jacobs-Sera
  • , David van Duin
  • , Barry N. Kreiswirth
  • Graham F. Hatfull, Anne Friedland
  • University of Pittsburgh
  • Center for Discovery and Innovation
  • Hackensack Meridian School of Medicine
  • University of North Carolina at Chapel Hill

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Nontuberculous mycobacterium (NTM) infections are challenging to manage and are frequently non-responsive to aggressive but poorly-tolerated antibiotic therapies. Immunosuppressed lung transplant patients are susceptible to NTM infections and poor patient outcomes are common. Bacteriophages present an alternative treatment option and are associated with favorable clinical outcomes. Similarly, dual beta-lactam combinations show promise in vitro, but clinical use is sparse. We report here a patient with an uncontrolled Mycobacterium abscessus infection following a bilateral lung transplant and failed antibiotic therapy. Both smooth and rough colony morphotype strains were initially present, but treatment with two phages that kill the rough strain – including epigenetic-modification to overcome restriction – resulted in isolation of only the smooth strain. The rough and smooth strains have similar antibiotic susceptibilities suggesting that the phages specifically eliminated the rough strain. Dual beta-lactam therapy with meropenem and ceftazidime-avibactam provided further clinical improvement, and the phages act synergistically with meropenem in vitro.

Original languageEnglish
Article number10360
JournalNature Communications
Volume15
Issue number1
DOIs
StatePublished - Dec 2024

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