Objectives: To assess the in vitro susceptibility of Francisella tularensis subsp. holarctica biovar II strains to 24 antimicrobial agents.

Methods: Thirty-nine F. tularensis strains isolated from humans in the Central Anatolia region of Turkey were examined. Each isolate was identified by conventional and molecular techniques. MICs of aminoglycosides, tetracyclines, fluoroquinolones, macrolides, penicillins, cephalosporins, imipenem, clindamycin, linezolid, chloramphenicol and rifampicin were determined using the Etest method on glucose/cysteine blood agar plates. Interpretation of results was made according to CLSI clinical breakpoints.

Results: All strains were susceptible to aminoglycosides, tetracyclines, chloramphenicol, rifampicin and three fluoroquinolones. In contrast, resistance to penicillins, cephalosporins, carbapenems, macrolides and clindamycin was observed for all isolates. Fluoroquinolones had the lowest MIC(50) and MIC(90).

Conclusions: All strains were susceptible to the antibiotics traditionally used to treat tularaemia, such as streptomycin (MIC(90) 1.5 mg/L), gentamicin (MIC(90) 0.25 mg/L), tetracycline (MIC(90) 0.38 mg/L) and chloramphenicol (MIC(90) 0.25 mg/L). Since fluoroquinolones showed the lowest MIC values, and have important advantages over aminoglycosides, including ease of oral administration and lower toxicities, quinolones have the potential for being effective first-line therapy for tularaemia.

Download full-text PDF

Source
http://dx.doi.org/10.1093/jac/dkr338DOI Listing

Publication Analysis

Top Keywords

francisella tularensis
8
tularensis subsp
8
subsp holarctica
8
strains isolated
8
isolated humans
8
humans central
8
central anatolia
8
anatolia region
8
region turkey
8
aminoglycosides tetracyclines
8

Similar Publications

Tularemia is a rare nationally notifiable zoonosis, caused by the tier-1 select agent Francisella tularensis, that has been reported from all U.S. states except Hawaii.

View Article and Find Full Text PDF

Unveiling the versatility of the thioredoxin framework: Insights from the structural examination of DsbA1.

Comput Struct Biotechnol J

December 2024

Department of Biochemistry and Chemistry, La Trobe Institute for Molecular Science, School of Agriculture, Biomedicine and Environment, La Trobe University, Bundoora, Australia.

In bacteria the formation of disulphide bonds is facilitated by a family of enzymes known as the disulphide bond forming (Dsb) proteins, which, despite low sequence homology, belong to the thioredoxin (TRX) superfamily. Among these enzymes is the disulphide bond-forming protein A (DsbA); a periplasmic thiol oxidase responsible for catalysing the oxidative folding of numerous cell envelope and secreted proteins. Pathogenic bacteria often contain diverse Dsb proteins with distinct functionalities commonly associated with pathogenesis.

View Article and Find Full Text PDF

in Wild Lagomorphs in Southern Spain's Mediterranean Ecosystems.

Animals (Basel)

November 2024

Grupo de Investigación en Sanidad Animal y Zoonosis (GISAZ), Departamento de Sanidad Animal, UIC Zoonosis y Enfermedades Emergentes ENZOEM, Universidad de Córdoba, 14014 Córdoba, Spain.

is a vector-borne zoonotic bacterium that causes tularemia, a disease of great importance for animal and public health. Although wild lagomorphs are considered one of the major reservoirs of this bacterium, information about the circulation of in European wild rabbit () and Iberian hare () populations in Europe is still very limited. In Spain, is present in northern central regions, with recurrent outbreaks occurring annually.

View Article and Find Full Text PDF

Tularemia is a re-emerging zoonosis in many endemic countries. It is caused by , a gram-negative bacterium and biological threat agent. Humans are infected from the wild animal reservoir, the environmental reservoir or by the bite of arthropod vectors.

View Article and Find Full Text PDF
Article Synopsis
  • - Human infections from a dangerous bacteria usually occur through contaminated sources like water and food, and the bacteria can survive in these environments for extended periods.
  • - A lab study demonstrated that this bacteria can remain viable in fresh water for 3 to 8 weeks at low temperatures, leading researchers to explore the genetic factors that support this persistence.
  • - The research identified a key gene, murein peptide ligase, which is essential for the bacteria’s survival in water and during stress, emphasizing the role of bacterial cell walls in adapting to various environmental challenges.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!