Susceptibility of Achromobacter spp. to bacteriophages and phage/antibiotic combinations

Achromobacter infections pose significant challenges to people with Cystic Fibrosis (CF). This microbe often becomes multidrug resistant (MDR) or extensively drug resistant (XDR), leaving physicians with few antibiotic treatment options. It is a growing problem in people with CF because it is difficult to eliminate with antibiotics, leading to chronic lung infections that increasingly acquire antibiotic resistance. We have been searching for alternative therapies for Achromobacter infection and identified a cadre of 26 bacteriophages (viruses that attack bacteria) that target it that could allow us to reduce reliance on antibiotics. We tested these phages against a collection of 56 MDR and XDR clinical Achromobacter isolates and found that all were susceptible to multiple of these phages. We also evaluated whether we could restore the activity of certain antibiotics by using them as adjunctive therapy to phage treatment in vitro. We found that when meropenem (a beta lactam antibiotic) was added to phage treatment, susceptibility to meropenem was demonstrated in many isolates regardless of whether the Achromobacter was initially susceptible to meropenem. The data presented here suggests that combination therapy using meropenem with an active phage should be considered for treatment of Achromobacter infections regardless of pre-existing antibiotic susceptibility.

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Publication Details

Journal
Communications Biology
Published
2026-11-03
DOI
https://doi.org/10.1038/s42003-026-11282-w
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Susceptibility of Achromobacter spp. to bacteriophages and phage/antibiotic combinations

Joe Pogliano, David T. Pride, Ana Georgina Cobián Güemes, Monica Bates et al.
Communications Biology
Bacteriophages and microbial interactions
article

Susceptibility of Achromobacter spp. to bacteriophages and phage/antibiotic combinations

Joe Pogliano, David T. Pride, Ana Georgina Cobián Güemes, Monica Bates, Douglas Conrad, Jesse Leonard, Natasha Kanhirun, Alicia Amamoto, Victoria Carrico, John Bradley, Zachary Pride, Andrew Su, Marine Tourneur, Bethzabe Serrano Buelna, Gabriel Koch, Joseph Oh, David Pride, Phoolwanti Rani, Yixian Huang, Norhan Turki, Alisha Blanc, Rob Knight
article en

Abstract

Achromobacter infections pose significant challenges to people with Cystic Fibrosis (CF). This microbe often becomes multidrug resistant (MDR) or extensively drug resistant (XDR), leaving physicians with few antibiotic treatment options. It is a growing problem in people with CF because it is difficult to eliminate with antibiotics, leading to chronic lung infections that increasingly acquire antibiotic resistance. We have been searching for alternative therapies for Achromobacter infection and identified a cadre of 26 bacteriophages (viruses that attack bacteria) that target it that could allow us to reduce reliance on antibiotics. We tested these phages against a collection of 56 MDR and XDR clinical Achromobacter isolates and found that all were susceptible to multiple of these phages. We also evaluated whether we could restore the activity of certain antibiotics by using them as adjunctive therapy to phage treatment in vitro. We found that when meropenem (a beta lactam antibiotic) was added to phage treatment, susceptibility to meropenem was demonstrated in many isolates regardless of whether the Achromobacter was initially susceptible to meropenem. The data presented here suggests that combination therapy using meropenem with an active phage should be considered for treatment of Achromobacter infections regardless of pre-existing antibiotic susceptibility.

Communications Biology
University of California San Diego (US), Rady Children's Hospital-San Diego (US)
National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 78%
Bacteriophages and microbial interactions
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