Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118

Acinetobacter baumannii A118, a strain isolated from the blood of an infected patient, is naturally competent and unlike most clinical strains, is susceptible to a variety of different antibiotics including those usually used for selection in genetic manipulations. These characteristics make strain...

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Main Authors: Maria S. Ramirez, William F. Penwell, German M. Traglia, Daniel L. Zimbler, Jennifer A. Gaddy, Nikolas Nikolaidis, Brock A. Arivett, Mark D. Adams, Robert A. Bonomo, Luis A. Actis, Marcelo E. Tolmasky
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-07-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2019.01599/full
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author Maria S. Ramirez
William F. Penwell
German M. Traglia
Daniel L. Zimbler
Jennifer A. Gaddy
Jennifer A. Gaddy
Nikolas Nikolaidis
Brock A. Arivett
Mark D. Adams
Robert A. Bonomo
Luis A. Actis
Marcelo E. Tolmasky
author_facet Maria S. Ramirez
William F. Penwell
German M. Traglia
Daniel L. Zimbler
Jennifer A. Gaddy
Jennifer A. Gaddy
Nikolas Nikolaidis
Brock A. Arivett
Mark D. Adams
Robert A. Bonomo
Luis A. Actis
Marcelo E. Tolmasky
author_sort Maria S. Ramirez
collection DOAJ
description Acinetobacter baumannii A118, a strain isolated from the blood of an infected patient, is naturally competent and unlike most clinical strains, is susceptible to a variety of different antibiotics including those usually used for selection in genetic manipulations. These characteristics make strain A118 a convenient model for genetic studies of A. baumannii. To identify potential virulence factors, its complete genome was analyzed and compared to other A. baumannii genomes. A. baumannii A118 includes gene clusters coding for the acinetobactin and baumannoferrin iron acquisition systems. Iron-regulated expression of the BauA outer membrane receptor for ferric-acinetobactin complexes was confirmed as well as the utilization of acinetobactin. A. baumannii A118 also possesses the feoABC genes, which code for the main bacterial ferrous uptake system. The functionality of baumannoferrin was suggested by the ability of A. baumannii A118 culture supernatants to cross feed an indicator BauA-deficient strain plated on iron-limiting media. A. baumannii A118 behaved as non-motile but included the csuA/BABCDE chaperone-usher pilus assembly operon and produced biofilms on polystyrene and glass surfaces. While a known capsular polysaccharide (K) locus was identified, the outer core polysaccharide (OC) locus, which belongs to group B, showed differences with available sequences. Our results show that despite being susceptible to most antibiotics, strain A118 conserves known virulence-related traits enhancing its value as model to study A. baumannii pathogenicity.
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spelling doaj.art-772963d8fbc340d0964b517251fc41972022-12-21T22:51:28ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2019-07-011010.3389/fmicb.2019.01599457645Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118Maria S. Ramirez0William F. Penwell1German M. Traglia2Daniel L. Zimbler3Jennifer A. Gaddy4Jennifer A. Gaddy5Nikolas Nikolaidis6Brock A. Arivett7Mark D. Adams8Robert A. Bonomo9Luis A. Actis10Marcelo E. Tolmasky11Department of Biological Science, Center for Applied Biotechnology Studies, California State University, Fullerton, Fullerton, CA, United StatesDepartment of Microbiology, Miami University, Oxford, OH, United StatesLaboratorio de Bacteriología Clínica, Departamento de Bioquímica Clínica, Facultad de Farmacia y Bioquímica, Hospital de Clínicas “José de San Martín”, Buenos Aires, ArgentinaDepartment of Microbiology, Miami University, Oxford, OH, United StatesDepartment of Microbiology, Miami University, Oxford, OH, United StatesDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United StatesDepartment of Biological Science, Center for Applied Biotechnology Studies, California State University, Fullerton, Fullerton, CA, United StatesDepartment of Microbiology, Miami University, Oxford, OH, United StatesDepartment of Genetics, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartments of Pharmacology and Molecular Biology and Microbiology, Louis Stokes Cleveland Veterans Affairs Medical Center, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Microbiology, Miami University, Oxford, OH, United StatesDepartment of Biological Science, Center for Applied Biotechnology Studies, California State University, Fullerton, Fullerton, CA, United StatesAcinetobacter baumannii A118, a strain isolated from the blood of an infected patient, is naturally competent and unlike most clinical strains, is susceptible to a variety of different antibiotics including those usually used for selection in genetic manipulations. These characteristics make strain A118 a convenient model for genetic studies of A. baumannii. To identify potential virulence factors, its complete genome was analyzed and compared to other A. baumannii genomes. A. baumannii A118 includes gene clusters coding for the acinetobactin and baumannoferrin iron acquisition systems. Iron-regulated expression of the BauA outer membrane receptor for ferric-acinetobactin complexes was confirmed as well as the utilization of acinetobactin. A. baumannii A118 also possesses the feoABC genes, which code for the main bacterial ferrous uptake system. The functionality of baumannoferrin was suggested by the ability of A. baumannii A118 culture supernatants to cross feed an indicator BauA-deficient strain plated on iron-limiting media. A. baumannii A118 behaved as non-motile but included the csuA/BABCDE chaperone-usher pilus assembly operon and produced biofilms on polystyrene and glass surfaces. While a known capsular polysaccharide (K) locus was identified, the outer core polysaccharide (OC) locus, which belongs to group B, showed differences with available sequences. Our results show that despite being susceptible to most antibiotics, strain A118 conserves known virulence-related traits enhancing its value as model to study A. baumannii pathogenicity.https://www.frontiersin.org/article/10.3389/fmicb.2019.01599/fullAcinetobactervirulence factorspathogenicityhospital infectioncommunity infectionESKAPE
spellingShingle Maria S. Ramirez
William F. Penwell
German M. Traglia
Daniel L. Zimbler
Jennifer A. Gaddy
Jennifer A. Gaddy
Nikolas Nikolaidis
Brock A. Arivett
Mark D. Adams
Robert A. Bonomo
Luis A. Actis
Marcelo E. Tolmasky
Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118
Frontiers in Microbiology
Acinetobacter
virulence factors
pathogenicity
hospital infection
community infection
ESKAPE
title Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118
title_full Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118
title_fullStr Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118
title_full_unstemmed Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118
title_short Identification of Potential Virulence Factors in the Model Strain Acinetobacter baumannii A118
title_sort identification of potential virulence factors in the model strain acinetobacter baumannii a118
topic Acinetobacter
virulence factors
pathogenicity
hospital infection
community infection
ESKAPE
url https://www.frontiersin.org/article/10.3389/fmicb.2019.01599/full
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