Acinetobacter species isolates from a range of environments: species survey and observations of antimicrobial resistance

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Abstract

Acinetobacter species isolates from a range of environments, including soil, were investigated. We determined 16S rRNA and rpoB gene sequences for species identification and performed tests of antimicrobial resistance susceptibility. Twenty-nine of the isolates (8 from soil and 21 from life environment) belonged to the genus Acinetobacter. Fourteen Acinetobacter species were identified among 29 isolates: 4 A. baumannii, 3 A. calcoaceticus, 1 A. nosocomialis, 2 A. pittii, and 2 Acinetobacter gen. sp. ‘close to 13TU’ as A. calcoaceticusbaumannii complex. Three Acinetobacter species isolates were identified as novel species candidates. Three Acinetobacter species isolates were resistant to imipenem: 1 A. parvus and 2 novel species candidates of Acinetobacter. Eight isolates showed resistance to colistin: all Acinetobacter gen. sp. ‘close to 13TU’ (2 isolates) and A. parvus isolates (3 isolates) were resistant to colistin. Although the genotypes of A. baumannii isolates from various natural environments were different from those of clinical isolates, the presence of clinically important and antimicrobial resistant Acinetobacter species in the natural environment may represent a threat to public health.

Introduction

Acinetobacter species are aerobic, nonmotile, Gram-negative coccobacillary rods and are commonly classified as nonfermentative bacteria along with Pseudomonas aeruginosa and Stenotrophomonas maltophilia. They have been implicated in pneumonia, urinary tract infections, skin and soft tissue infections, and bloodstream infections (Lee and Ko, 2012). Although Acinetobacter species were viewed as colonizers and often ignored in clinical settings until the 1980s, they have emerged as major causal agents of healthcare-associated infections, particularly in immunocompromised patients and patients in intensive care units (Munoz-Price and Weinstein, 2008). Acinetobacter species are ubiquitous within the environment and are found in soil, water, and on the dry surfaces of diverse devices. The ability to persist in diverse environments makes Acinetobacter species one of the most common pathogens in hospitals (Espinal et al., 2012). In addition to nosocomial infections, recent reports suggest that Acinetobacter species cause community-acquired infections (Falagas et al., 2007, Kang et al., 2012). Thus, environmental exposure to Acinetobacter species should not be ignored as a potential agent of disease. Although the species distribution and antimicrobial resistance of Acinetobacter species isolates from hospitals are well studied, those of environmental Acinetobacter species isolates have not (Zeana et al., 2003).

In this study, we describe the isolation of Acinetobacter species from a range of environments, including soil. Species identification was performed via 16S rRNA and partial rpoB gene sequencing, and antimicrobial resistance was also investigated. Several isolates of A. baumannii, the most important nosocomial pathogen among the Acinetobacter species, were identified, and antimicrobial-resistant Acinetobacter species isolates, including imipenem-resistant or colistin-resistant isolates, were also found.

Section snippets

Bacterial isolation

To obtain microorganisms from soil, soils were sampled in 7 different locations in South Korea (Table 1). One gram of soil sample was suspended in 10 mL of distilled water and diluted 1:50. The diluted soil sample was spread on blood agar and incubated at 30 °C for 24 h. Microorganisms were also isolated from various life environments, which are defined in this study as artificial environments excluding soil, water, air, etc., near where the soil samples were obtained using sterilized cotton

Results

As a result of bacterial identification of 409 isolates using 16S rRNA gene sequencing, genus Bacillus was the most predominant (173 isolates). In addition to Bacillus, Arthrobacter, Psychrobacter, Acinetobacter, Aeromonas, and Pseudomonas were also frequently isolated. A total of 29 isolates were isolated from soil and life environment and identified to belong to the genus Acinetobacter based on 16S rRNA gene sequence analysis. While 20 of the 29 isolates showed ≥ 99% 16S rRNA gene sequence

Discussion

In this study, we observed the diversity of Acinetobacter species isolates obtained from a range of environments. Three previously described Acinetobacter species and 3 new species candidates were identified from soil, and 10 previously described Acinetobacter species and 3 genomic species were identified from life environment. One of the most important findings may be the identification of nosocomial human pathogens such as A. baumannii, A. nosocomialis, A. pittii, and Acinetobacter gen. sp.

References (21)

  • T. Adékambi et al.

    The rpoB gene as a tool for clinical microbiologists

    Trend Microbiol

    (2009)
  • P. Espinal et al.

    Effect of biofilm formation on the survival of Acinetobacter baumannii on dry surfaces

    J Hosp Infect

    (2012)
  • J.Y. Lee et al.

    Antimicrobial resistance and clones of Acinetobacter species and Pseudomonas aeruginosa

    J Bact Virol

    (2012)
  • M.D. Adams et al.

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

    Antimicrob Agents Chemother

    (2009)
  • L.A. Arroyo et al.

    The pmrCAB operon mediates polymyxin resistance in Acinetobacter baumannii ATCC 17978 and clinical isolates through phosphoethanolamine modification of lipid A

    Antimicrob Agents Chemother

    (2011)
  • S.G. Bartual et al.

    Development of a multilocus sequence typing scheme for characterization of clinical isolates of Acinetobacter baumannii

    J Clin Microbiol

    (2005)
  • Clinical and Laboratory Standards Institute (CLSI)

    Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically; approved standard - eighth edition, M07-A8

    (2009)
  • Clinical and Laboratory Standards Institute (CLSI)

    Performance standards for antimicrobial susceptibility testing: 21st informational supplement (M100-S21)

    (2011)
  • M. Drancourt et al.

    Systematic 16S rRNA gene sequencing of atypical clinical isolates identified 27 new bacterial species associated with humans

    J Clin Microbiol

    (2004)
  • M.E. Falagas et al.

    Community-acquired Acinetobacter infections

    Eur J Clin Microbiol Infect Dis

    (2007)
There are more references available in the full text version of this article.

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This study was partially supported by grants from the National Institute of Environment Research, South Korea.

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