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Acinetobacter baumannii Resistant to Colistin With Impaired Virulence: A Case Report From France

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TLDR
The clinical case of a French patient colonized with an A. baumannii colistin-resistant isolate aftercolistin therapy without clinical signs of infection is reported.
Abstract
To the Editor—In an article recently published in the Journal, Lopez-Rojas et al [1] demonstrated that an in vitro mutant of Acinetobacter baumannii resistant to colistin had reduced in vivo fitness and decreased virulence, in terms of both mortality and survival, in a mouse model of peritoneal sepsis. They suggest that the lower in vivo bacterial fitness and decreased virulence of this mutant may explain the low incidence of colistin resistance in the clinical setting. We report herein the clinical case of a French patient colonized with an A. baumannii colistin-resistant isolate after colistin therapy without clinical signs of infection. A 58-year-old patient presented with an influenzalike illness on 16 December 2010 and was treated at home with ampicillin-clavulanic acid. On day 3, he was admitted at Salon de Provence hospital for dyspnea, fever, and right lobar pneumonia on chest x-ray. On day 7, the patient required mechanical ventilation after endotracheal intubation for acute respiratory failure. Antibiotherapy was switched to piperacillin-tazobactam and spiramycin. A bronchoalveolar lavage (BAL) sampled at that time was sterile, and influenza virus detection was negative. Treatment was switched to imipenem-amikacin on day 15 for acute respiratory distress syndrome and septic shock. On day 19, extracorporeal membrane oxy-genation (ECMO) was started for re-fractory hypoxemia, and the patient was referred to an intensive care unit (ICU) in Marseille. On day 21, a colistin-susceptible A. baumannii isolate was recovered from BAL, as well as from 3 blood cultures. Treatment was switched to intravenous colistin and rifampin. ECMO was weaned and sedation was stopped on day 27. Colistin and rifampin were stopped on day 35 but a treatment using imipenem-amikacin-colistin was started on day 37 for a new septic shock episode and stopped on day 41, based on negative BAL and blood cultures. While respiratory status improved, tracheal colonization with colistin-resistant A. baumannii was detected from day 50 to day 60 on biweekly endotracheal aspirate cultures. No clinical sign of infection was present during this period. Asymptomatic bacteri-uria to colistin-sensitive A. baumannii was also present by day 50 and was treated with bladder instillations of colistin from day 57. Treatment was stopped on day 67 when colistin-resistant A. baumannii was isolated from urine samples. The patient was discharged alive from the ICU on day 70. Our case report confirms that colistin-resistant A. baumannii strains may be selected in vivo by the use of colistin but that colistin-resistant strains may be …

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Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria

TL;DR: Current knowledge concerning the different strategies bacteria employ to resist the activities of polymyxins are summarized and increased understanding of these mechanisms is extremely vital and timely to facilitate studies of antimicrobial peptides and find new potential drugs targeting clinically relevant Gram-negative bacteria.
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Antimicrobial Resistance and Virulence: a Successful or Deleterious Association in the Bacterial World?

TL;DR: This review considers how bacterial virulence and fitness are affected by antibiotic resistance and also how the relationship between virulent and resistance is affected by different genetic mechanisms and by the most prevalent global responses.
Journal ArticleDOI

Colistin resistance of Acinetobacter baumannii: clinical reports, mechanisms and antimicrobial strategies

TL;DR: Pharmacokinetic/pharmacodynamic studies revealed that colistin monotherapy is unable to prevent resistance, and combination therapy might be the best antimicrobial strategy againstcolistin-resistant A. baumannii.
Journal ArticleDOI

Colistin: an update on the antibiotic of the 21st century.

TL;DR: It is probable that colistin will be the ‘last-line’ therapeutic drug against multidrug-resistant Gram-negative pathogens in the 21st century.
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Emergence of resistance to carbapenems in Acinetobacter baumannii in Europe: clinical impact and therapeutic options.

TL;DR: Current knowledge about A. baumannii, including biological and epidemiological aspects as well as resistance to antibiotics and antibiotic therapy, are reviewed in this article, in addition to therapeutic recommendations.
References
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Journal ArticleDOI

Acinetobacter baumannii: Emergence of a Successful Pathogen

TL;DR: This review details the significant advances that have been made in understanding of this remarkable organism over the last 10 years, including current taxonomy and species identification, issues with susceptibility testing, mechanisms of antibiotic resistance, global epidemiology, clinical impact of infection, host-pathogen interactions, and infection control and therapeutic considerations.
Journal ArticleDOI

Antibiotic resistance and its cost: is it possible to reverse resistance?

TL;DR: The findings suggest that the fitness costs of resistance will allow susceptible bacteria to outcompete resistant bacteria if the selective pressure from antibiotics is reduced, and that the rate of reversibility will be slow at the community level.
Journal ArticleDOI

Colistin Resistance in Acinetobacter baumannii Is Mediated by Complete Loss of Lipopolysaccharide Production

TL;DR: It is shown that A. baumannii can rapidly develop resistance to polymyxin antibiotics by complete loss of the initial binding target, the lipid A component of lipopolysaccharide (LPS), which has long been considered to be essential for the viability of Gram-negative bacteria.
Journal ArticleDOI

Resistance to colistin in Acinetobacter baumannii associated with mutations in the PmrAB two-component system

TL;DR: expression of pmrA was increased in Colr mutants, but not at a low pH, suggesting that additional regulatory factors remain to be discovered, and growth in ferric chloride conferred a small protective effect.
Journal ArticleDOI

New Delhi metallo-beta-lactamase (NDM-1): towards a new pandemia?

TL;DR: The New Delhi metallo-beta-lactamase (NDM-1) is a novel type of MBL named after the city of origin, which has been recently criticized, following a common practice with transferable MBLs since VIM-1 was named after Verona, Italy.
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