Investigation of the Virulence Factors and Molecular Characterization of the Clonal Relations of Multidrug-Resistant Acinetobacter baumannii Isolates

Author:

Ali Hayssam M1,Salem Mohamed Z M2,El-Shikh Mohamed S3,Megeed Ahmed Abdel4,Alogaibi Yahya A5,Talea Ibrahim Ahmed6

Affiliation:

1. King Saud University, College of Science, Department of Botany and Microbiology, PO Box 2455, Riyadh 11451, Saudi Arabia Agriculture ResearchCenter, Horticulture Research Institute, Sabahia Horticulture Research Station,Department of Timber Trees Research, Alexandria, Egypt

2. Alexandria University, Faculty of Agriculture (EL-Shatby), Department of Forestry and Wood Technology, Alexandria, Egypt

3. King Saud University, College of Science, Department of Botany and Microbiology, PO Box 2455, Riyadh 11451, Saudi Arabia

4. Plant Protection Department Faculty of Agriculture Alexandria University, Egypt

5. Department of Orthodontics, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia

6. Riyadh Colleges of Dentistry and Pharmacy, Riyadh, Saudi Arabia

Abstract

Abstract Multidrug-resistant (MDR) Acinetobacter baumannii infections are a great public health concern and demand continuous surveillance and antibiotic stewardship. Virulence traits and the pathogenicity of Acinetobacter are less studied compared with the molecular epidemiological and antibiotic resistance profile of this organism. In our present study, we investigated the primary characteristics contributing to the virulence of MDR A. baumannii isolates and compared them with avirulent isolates. Atotal of 32 well-characterized MDR A. baumannii clinical isolates and 22 avirulent isolates from a healthy individual were subjected to multilocus sequence typing and polymerase chain reaction (PCR) for a variety of biofilm-associated genes. Additionally, a number of in vitro tests were performed to determine virulence properties. Isolates were found to relate to six sequence types (STs) in which the dominant sequence was ST557 in clinical isolates, followed by ST195 and ST208. However, ST557 and ST222 were absent in avirulent isolates. All STs belonged to clonal complex 2 and clonal lineage 2, which is considered to be a universal clone. PCR analysis showed that most clinical isolates were positive for biofilm-forming genes, such as csu and bap, and also carried pga and ompA genes, which were less common in avirulentisolates. Biofilm formation, phospholipase C production, hemolytic activity, and acinetobactin production occurred significantly more frequently in clinical isolates compared with avirulent isolates. Though A. baumannii clonal lineages showed common virulence traits, they differed in virulent phenotype expression. These findings further support previous studies indicating that A. baumannii is a versatile pathogen with an ability to acquire iron and survive in iron-limiting conditions, highlighting the acinetobactin-mediated iron acquisition mechanisms involved in the pathogenesis of A. baumannii infections.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology,Agronomy and Crop Science,Environmental Chemistry,Food Science,Analytical Chemistry

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