Inhibition of pseudomonas aeruginosa by peptide-conjugated phosphorodiamidate morpholino oligomers

James J. Howard, Carolyn R. Sturge, Dina A. Moustafa, Seth M. Daly, Kimberly R. Marshall-Batty, Christina F. Felder, Danniel Zamora, Marium Yabe-Gill, Maria Labandeira-Rey, Stacey M. Bailey, Michael Wong, Joanna B. Goldberg, Bruce L. Geller, David E. Greenberg

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Pseudomonas aeruginosa is a highly virulent, multidrug-resistant pathogen that causes significant morbidity and mortality in hospitalized patients and is particularly devastating in patients with cystic fibrosis. Increasing antibiotic resistance coupled with decreasing numbers of antibiotics in the developmental pipeline demands novel antibacterial approaches. Here, we tested peptide-conjugated phosphorodiamidate morpholino oligomers (PPMOs), which inhibit translation of complementary mRNA from specific, essential genes in P. aeruginosa. PPMOs targeted to acpP, lpxC, and rpsJ, inhibited P. aeruginosa growth in many clinical strains and activity of PPMOs could be enhanced 2- to 8-fold by the addition of polymyxin B nonapeptide at subinhibitory concentrations. The PPMO targeting acpP was also effective at preventing P. aeruginosa PAO1 biofilm formation and at reducing existing biofilms. Importantly, treatment with various combinations of a PPMO and a traditional antibiotic demonstrated synergistic growth inhibition, the most effective of which was the PPMO targeting rpsJ with tobramycin. Furthermore, treatment of P. aeruginosa PA103-infected mice with PPMOs targeting acpP, lpxC, or rpsJ significantly reduced the bacterial burden in the lungs at 24 h by almost 3 logs. Altogether, this study demonstrates that PPMOs targeting the essential genes acpP, lpxC, or rpsJ in P. aeruginosa are highly effective at inhibiting growth in vitro and in vivo. These data suggest that PPMOs alone or in combination with antibiotics represent a novel approach to addressing the problems associated with rapidly increasing antibiotic resistance in P. aeruginosa.

Original languageEnglish (US)
Article numbere01938
JournalAntimicrobial Agents and Chemotherapy
Volume61
Issue number4
DOIs
StatePublished - Apr 1 2017

Fingerprint

Morpholinos
Pseudomonas aeruginosa
Peptides
Essential Genes
Biofilms
Microbial Drug Resistance
Anti-Bacterial Agents
Growth
Tobramycin
Protein Biosynthesis
Cystic Fibrosis
Morbidity
Lung
Mortality

Keywords

  • Antibiotic resistance
  • Antimicrobial agents
  • Antisense
  • Experimental therapeutics
  • Phosphorodiamidate morpholino oligomer
  • PPMO
  • Pseudomonas aeruginosa

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

Cite this

Inhibition of pseudomonas aeruginosa by peptide-conjugated phosphorodiamidate morpholino oligomers. / Howard, James J.; Sturge, Carolyn R.; Moustafa, Dina A.; Daly, Seth M.; Marshall-Batty, Kimberly R.; Felder, Christina F.; Zamora, Danniel; Yabe-Gill, Marium; Labandeira-Rey, Maria; Bailey, Stacey M.; Wong, Michael; Goldberg, Joanna B.; Geller, Bruce L.; Greenberg, David E.

In: Antimicrobial Agents and Chemotherapy, Vol. 61, No. 4, e01938, 01.04.2017.

Research output: Contribution to journalArticle

Howard, JJ, Sturge, CR, Moustafa, DA, Daly, SM, Marshall-Batty, KR, Felder, CF, Zamora, D, Yabe-Gill, M, Labandeira-Rey, M, Bailey, SM, Wong, M, Goldberg, JB, Geller, BL & Greenberg, DE 2017, 'Inhibition of pseudomonas aeruginosa by peptide-conjugated phosphorodiamidate morpholino oligomers', Antimicrobial Agents and Chemotherapy, vol. 61, no. 4, e01938. https://doi.org/10.1128/AAC.01938-16
Howard, James J. ; Sturge, Carolyn R. ; Moustafa, Dina A. ; Daly, Seth M. ; Marshall-Batty, Kimberly R. ; Felder, Christina F. ; Zamora, Danniel ; Yabe-Gill, Marium ; Labandeira-Rey, Maria ; Bailey, Stacey M. ; Wong, Michael ; Goldberg, Joanna B. ; Geller, Bruce L. ; Greenberg, David E. / Inhibition of pseudomonas aeruginosa by peptide-conjugated phosphorodiamidate morpholino oligomers. In: Antimicrobial Agents and Chemotherapy. 2017 ; Vol. 61, No. 4.
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