Related Experiment Video
Updated: Aug 8, 2025

08:23
Culture Methods to Determine the Limit of Detection and Survival in Transport Media of Campylobacter Jejuni in Human Fecal Specimens
Published on: March 10, 2020
11.7K
Campylobacter fetus Cellulitis.
Lia Bastos1, Ricardo Gomes2, Sara Pocinho1
1Infectious Diseases and Tropical Medicine, Centro Hospitalar de Lisboa Ocidental, Lisbon, PRT.
Cureus
|February 27, 2023
Summary
Campylobacter fetus, a rare cause of cellulitis, can lead to severe systemic infections in vulnerable individuals. Early diagnosis via blood culture and appropriate antibiotic treatment are crucial for patient outcomes.
Area of Science:
- Medical Microbiology
- Infectious Diseases
- Bacteriology
Background:
- Campylobacter fetus is a bacterial species known for causing systemic infections, often presenting outside the gastrointestinal tract.
- Human infections are infrequent and typically occur in immunocompromised individuals or the elderly, with cattle and sheep serving as primary reservoirs.
Observation:
- This report details a rare case of cellulitis caused by Campylobacter fetus in a susceptible patient.
- Diagnosis was confirmed through blood cultures, highlighting the pathogen's tendency for endovascular invasion.
Findings:
- The likely source of infection in this case was consumption of fresh cheese, differing from common associations with undercooked poultry or meat.
- A combination of carbapenem and gentamicin demonstrated improved outcomes and reduced relapse rates in patients with prior antibiotic exposure.
Implications:
- The study underscores the importance of considering Campylobacter fetus in non-intestinal infections, especially in at-risk populations.
- Effective treatment involves a combination antibiotic regimen and a four-week duration, though further research on optimal treatment duration is warranted due to antigenic variation contributing to relapses.
More Related Videos
Related Concept Videos
Bacterial Phylum Chlamydiae
69
The phylum Chlamydiae or Chlamydiota is composed of a single order, Chlamydiales. This phylum consists entirely of obligate intracellular parasites that infect eukaryotic hosts. While human pathogens within this group have been studied extensively, the phylum encompasses many species capable of interacting with various eukaryotic organisms. Members of Chlamydiae are typically small cocci, approximately 0.5 μm in diameter, and exhibit a distinctive developmental cycle. As is characteristic...
69
Stringent Response in E. coli
33
Bacterial growth is closely tied to nutrient availability, with cells proliferating exponentially under favorable conditions and entering a stationary phase when resources become scarce. This transition is mediated by a regulatory mechanism known as the stringent response, which allows bacteria to adapt to nutrient deprivation by modulating gene expression and metabolic activity.During nutrient scarcity, intracellular amino acid levels decline. It results in the accumulation of uncharged tRNAs...
33
Acute Pyelonephritis II: Diagnostic Studies and Management
26
Introduction:For diagnosing acute pyelonephritis, a comprehensive patient history is collected to identify symptoms such as dysuria, frequent or urgent urination, flank pain, or costovertebral angle (CVA) tenderness that may suggest a kidney infection.Physical ExaminationDuring the physical examination, CVA tenderness is assessed. This involves gentle percussion over the costovertebral angle, where tenderness often indicates a kidney infection.Diagnostic TestsUrinalysis: Used to identify white...
26
Cystic Fibrosis: Pathogenesis
320
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
320

