Target intelligence / Profile preview

Aeromonas hydrophila (A. hydrophila)

Target
A. hydrophila
Molecular classification
Other
01

Overview

Aeromonas hydrophila is a heterotrophic, Gram-negative, rod-shaped bacterium primarily found in aquatic environments (StatPearls, 2023). While it is a significant pathogen in fish and amphibians, it is also an opportunistic human pathogen capable of causing a range of illnesses, including gastroenteritis, skin and soft tissue infections, and life-threatening septicemia (CDC, 2022). The pathogenicity of A. hydrophila is mediated by a variety of virulence factors, such as aerolysin, cytotoxic enterotoxins, and various extracellular enzymes like proteases and lipases (PubMed, 2021). In clinical settings, it is often resistant to many common antibiotics, including penicillins and some cephalosporins, due to the production of multiple beta-lactamases (NIH, 2020). Treatment typically involves fluoroquinolones, aminoglycosides, or third-generation cephalosporins, which target essential bacterial processes like DNA replication and protein synthesis (Journal of Clinical Microbiology, 2019). Because Aeromonas hydrophila is a whole organism rather than a specific protein or receptor, it is classified as a pathogen rather than a molecular drug target (Microbiology Society, 2022). However, specific components of the bacterium, such as its DNA gyrase or ribosomes, serve as the actual molecular targets for antimicrobial therapy (Nature Reviews Microbiology, 2020). Monitoring for this organism often involves culture-based methods or molecular techniques like PCR to detect specific virulence genes (Clinical Infectious Diseases, 2021).

Other names
Bacillus hydrophilusProteus hydrophilusAeromonas punctataAeromonas liquefaciensA. hydrophila
02

Mechanism of action

Antibiotics used against Aeromonas hydrophila function through various mechanisms: fluoroquinolones inhibit DNA gyrase and topoisomerase IV, preventing DNA replication; aminoglycosides and tetracyclines inhibit protein synthesis by binding to ribosomal subunits; and beta-lactams (cephalosporins and carbapenems) inhibit peptidoglycan synthesis in the bacterial cell wall.

03

Biological functions

Other
04

Disease associations

Infection
05

Safety considerations

High prevalence of multidrug resistanceInducible chromosomal beta-lactamases (e.g., AmpC, CphA)Risk of rapid tissue destruction in necrotizing fasciitisPotential for sepsis in patients with underlying liver disease or immunosuppression
06

Interacting drugs

Ciprofloxacin

9 more in the full profile.

07

Biomarkers

Detection of aerolysin (aerA) and hemolysin (hlyA) genes16S rRNA gene sequencingPositive culture from sterile sitesMatrix-Assisted Laser Desorption/Ionization Time-of-Flight (MALDI-TOF) mass spectrometry identification

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