Phenotypical and molecular characterization of Acinetobacter spp. isolated from a pharmaceutical facility

Abstract Characterizing microorganisms according to different criteria is useful when investigating sources of microbiological contamination in the pharmaceutical industry. The aim of this study was to characterize 38 Acinetobacter baumannii complex strains isolated from a biopharmaceutical industry...

Full description

Saved in:
Bibliographic Details
Published inLetters in applied microbiology Vol. 76; no. 9
Main Authors Vasconcellos, Luiza, Silva, Samara Verly, da Costa, Luciana Veloso, de Miranda, Rebeca Vitoria da Silva Lage, dos Reis, Cristhiane Moura Falavina, Braga, Lygia Maria Paulo da Silva, Silva, Claudiane, Conceição, Greice, Mattoso, Josiane, Silva, Igor Barbosa, Forsythe, Stephen J, Midlej, Victor, Boas, Maria Helena Simões Villas, Brandão, Marcelo Luiz Lima
Format Journal Article
LanguageEnglish
Published 01.09.2023
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract Characterizing microorganisms according to different criteria is useful when investigating sources of microbiological contamination in the pharmaceutical industry. The aim of this study was to characterize 38 Acinetobacter baumannii complex strains isolated from a biopharmaceutical industry by 16S rRNA sequencing, matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI–TOF/MS), multilocus sequence typing (MLST), antimicrobial susceptibility profile, biofilm formation, and sensibility to disinfectants. Thirty-three (86.9%) strains were identified by 16S rRNA gene sequencing as A. seifertii/pitti/nosocomialis/lactucae, four (10.5%) as A. baumannii, and one (2.6%) as A. vivianii/courvalini. MALDI–TOF/MS did not identify one strain, and incorrectly identified 30/37 (81.1%) strains as A. baumannii. Strains were assigned to 12 different STs, of which nine were newly defined in this study (STs 2091–2099). Twenty-six (68.4%) strains showed resistance to amikacin and gentamicin. Thirty-three (86.8%) strains were classified as moderately or strongly adherent on polystyrene. Alcohol 70%/15 min and quaternary ammonium 0.08%/20 min were not able to eliminate the biofilm formed, but sodium hypochlorite 0.1%/15 min was efficient. In conclusion, improved methods are needed to improve the identification of Acinetobacter strains in pharmaceutical industries. This organism is of particular concern as it forms recalcitrant biofilms, leading to persistence in the manufacturing environment and increased risk of product contamination.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1472-765X
1472-765X
DOI:10.1093/lambio/ovad101