Literature DB >> 30217850

Chronic Airway Colonization by Achromobacter xylosoxidans in Cystic Fibrosis Patients Is Not Sustained by Their Domestic Environment.

Chloé Dupont1,2, Estelle Jumas-Bilak3,2, Clara Doisy3, Fabien Aujoulat3, Raphaël Chiron3,4, Hélène Marchandin3,5.   

Abstract

Achromobacter spp. are nonfermentative Gram-negative bacilli considered emergent pathogens in cystic fibrosis (CF). Although some cross-transmission events between CF patients have been described, Achromobacter strains were mostly patient specific, suggesting sporadic acquisitions from nonhuman reservoirs. However, sources of these emergent CF pathogens remain unknown. A large collection of specimens (n = 273) was sampled in the homes of 3 CF patients chronically colonized by Achromobacter xylosoxidans with the aim of evaluating the potential role of domestic reservoirs in sustaining airway colonization of the patients. Samples were screened for the presence of Achromobacter by using genus-specific molecular detection. Species identification, multilocus genotypes, and antimicrobial susceptibility patterns observed for environmental isolates were compared with those of clinical strains. Patient homes hosted a high diversity of Achromobacter species (n = 7), including Achromobacter mucicolens and A. animicus, two species previously isolated from human samples only, and genotypes (n = 15), all showing an overall susceptibility to antimicrobial agents. Achromobacter strains were mostly isolated from indoor moist environments and siphons, which are potential reservoirs for several CF emerging pathogens. A. xylosoxidans, the worldwide prevalent species colonizing CF patients, was not the major Achromobacter species inhabiting domestic environments. A. xylosoxidans genotypes chronically colonizing the patients were not detected in their household environments. These results support the notions that the domestic environment could not be incriminated in sustained patient colonization and that after initial colonization, the environmental survival of A. xylosoxidans clones adapted to the CF airways is probably impaired.IMPORTANCE Achromobacter spp. are worldwide emerging opportunistic pathogens in CF patients, able to chronically colonize the respiratory tract. Apart from regular consultations at the hospital CF center, patients spend most of their time at home. Colonization from nonhuman sources has been suggested, but the presence of Achromobacter spp. in CF patients' homes has not been explored. The domestic environments of CF patients chronically colonized by Achromobacter, especially wet environments, host several opportunistic pathogens, including a large diversity of Achromobacter species and genotypes. However, Achromobacter genotypes colonizing the patients were not detected in their domestic environments, making it unlikely that a shuttle between environment and CF airways is involved in persisting colonization. This also suggests that once the bacteria have adapted to the respiratory tract, their survival in the domestic environment is presumably impaired. Nevertheless, measures for reducing domestic patient exposure should be targeted on evacuation drains, which are frequently contaminated by CF opportunistic pathogens.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  Achromobacter; antimicrobial resistance; chronic colonization; cystic fibrosis; diversity; domestic environment; drains; habitat; reservoir

Mesh:

Year:  2018        PMID: 30217850      PMCID: PMC6238067          DOI: 10.1128/AEM.01739-18

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  34 in total

1.  Marked increase in incidence of Achromobacter xylosoxidans infections caused by sporadic acquisition from the environment.

Authors:  Winnie Ridderberg; Karen E M Bendstrup; Hanne V Olesen; Søren Jensen-Fangel; Niels Nørskov-Lauritsen
Journal:  J Cyst Fibros       Date:  2011-08-10       Impact factor: 5.482

2.  Persistent Bordetella bronchiseptica infection in a child with cystic fibrosis: Relationship to bacterial phenotype.

Authors:  Nevine El Khatib; Agnes Ferroni; Muriel Le Bourgeois; Frederique Chedevergne; Marlene Clairicia; Helene Avril; Nicole Guiso; I Sermet-Gaudelus
Journal:  J Cyst Fibros       Date:  2015-04-18       Impact factor: 5.482

3.  Persisting transmission of carbapenemase-producing Klebsiella pneumoniae due to an environmental reservoir in a university hospital, France, 2012 to 2014.

Authors:  Béatrice Clarivet; Delphine Grau; Estelle Jumas-Bilak; Hélène Jean-Pierre; Alix Pantel; Sylvie Parer; Anne Lotthé
Journal:  Euro Surveill       Date:  2016-04-28

4.  Shared genotypes of Achromobacter xylosoxidans strains isolated from patients at a cystic fibrosis rehabilitation center.

Authors:  Sabine Van Daele; Rita Verhelst; Geert Claeys; Gerda Verschraegen; Hilde Franckx; Leen Van Simaey; Catharine de Ganck; Frans De Baets; Mario Vaneechoutte
Journal:  J Clin Microbiol       Date:  2005-06       Impact factor: 5.948

5.  Contaminated sinks in intensive care units: an underestimated source of extended-spectrum beta-lactamase-producing Enterobacteriaceae in the patient environment.

Authors:  D Roux; B Aubier; H Cochard; R Quentin; N van der Mee-Marquet
Journal:  J Hosp Infect       Date:  2013-09-03       Impact factor: 3.926

6.  Changes in cystic fibrosis sputum microbiology in the United States between 1995 and 2008.

Authors:  Julia Emerson; Sharon McNamara; Anne Marie Buccat; Kelly Worrell; Jane L Burns
Journal:  Pediatr Pulmonol       Date:  2010-04

7.  Differential habitat use and niche partitioning by Pseudomonas species in human homes.

Authors:  Susanna K Remold; Christopher K Brown; Justin E Farris; Thomas C Hundley; Jessica A Perpich; Megan E Purdy
Journal:  Microb Ecol       Date:  2011-04-19       Impact factor: 4.552

8.  Use of nrdA gene sequence clustering to estimate the prevalence of different Achromobacter species among Cystic Fibrosis patients in the UK.

Authors:  Amy Coward; Dervla T D Kenna; Claire Perry; Kate Martin; Michel Doumith; Jane F Turton
Journal:  J Cyst Fibros       Date:  2015-09-26       Impact factor: 5.482

9.  First isolation of two colistin-resistant emerging pathogens, Brevundimonas diminuta and Ochrobactrum anthropi, in a woman with cystic fibrosis: a case report.

Authors:  Magalie Menuet; Fadi Bittar; Nathalie Stremler; Jean-Christophe Dubus; Jacques Sarles; Didier Raoult; Jean-Marc Rolain
Journal:  J Med Case Rep       Date:  2008-12-05

10.  Spread from the Sink to the Patient: In Situ Study Using Green Fluorescent Protein (GFP)-Expressing Escherichia coli To Model Bacterial Dispersion from Hand-Washing Sink-Trap Reservoirs.

Authors:  Shireen Kotay; Weidong Chai; William Guilford; Katie Barry; Amy J Mathers
Journal:  Appl Environ Microbiol       Date:  2017-03-31       Impact factor: 4.792

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  1 in total

1.  Longitudinal Surveillance and Combination Antimicrobial Susceptibility Testing of Multidrug-Resistant Achromobacter Species from Cystic Fibrosis Patients.

Authors:  Ijeoma N Okoliegbe; Karolin Hijazi; Kim Cooper; Corinne Ironside; Ian M Gould
Journal:  Antimicrob Agents Chemother       Date:  2020-10-20       Impact factor: 5.191

  1 in total

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