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DNA Sequencing to Evaluate Nail Pathogens: An Investigation into Bacteria and Fungi
Background:
It is well established and accepted that fungi are a major contributing factor in nail dystrophy. It has also been recognized that bacteria play a crucial role in onycholysis. However, the bacteria and fungi that can be grown on culture media in the laboratory are only a small fraction of the total diversity that exists in nature. Contemporary studies have revealed that fungi and bacteria often form physically and metabolically interdependent consortia that harbor properties and pathogenicity distinct from those of their individual components. Metagenomic DNA "shotgun" sequencing has proved useful in determining microbial etiology in clinical samples, effective for not only bacteria but also fungi, archaea, and viruses.
Methods:
Thirty-nine consecutive nail and subungual debris samples with suspected onychomycosis were sent for laboratory analysis using three examination techniques: DNA sequencing, polymerase chain reaction analysis, and standard fungal culture. The nail plate and surrounding areas were disinfected with an ethyl alcohol swab before nail sampling. Samples from 16 patients were analyzed for suspected onychomycosis with DNA sequencing, searching a database of 25,000 known pathogens. These results were compared with 15 real-time polymerase chain reaction screening assays and eight fungal cultures sampled with the same methods.
Results:
The DNA sequencing detected 32 species of bacteria and 28 species of fungi: 50% were solely bacterial, 6.3% were solely fungal, and 43.7% were mixed communities of bacteria and fungi.
Conclusions:
Toenails tested with DNA sequencing demonstrated the presence of both bacteria and fungi in many samples. Further work is required to fully investigate its relevance to nail pathology and treatment.
Insights
DNA sequencing reveals that toenail samples often contain both bacteria and fungi, indicating mixed microbial communities are common in nail conditions. This finding highlights the complex interplay of microbes in nail pathology.
Area of Science:
- Medical Mycology
- Clinical Microbiology
- Molecular Diagnostics
Background:
- Fungi are established causes of nail dystrophy, and bacteria are implicated in onycholysis.
- Laboratory cultures detect only a fraction of microbial diversity, missing interdependent bacterial and fungal consortia.
- Metagenomic DNA shotgun sequencing is a powerful tool for identifying diverse microbes, including bacteria, fungi, archaea, and viruses, in clinical samples.
Purpose of the Study:
- To compare the diagnostic yield of DNA sequencing with traditional methods for identifying microbial pathogens in suspected onychomycosis.
- To investigate the presence and diversity of bacterial and fungal communities in nail and subungual debris samples.
Main Methods:
- Nail and subungual debris samples from 39 patients with suspected onychomycosis were analyzed.
- Three techniques were employed: DNA sequencing, polymerase chain reaction (PCR) analysis, and standard fungal culture.
- DNA sequencing involved searching a database of 25,000 known pathogens and was compared against 15 real-time PCR assays and 8 fungal cultures.
Main Results:
- DNA sequencing identified 32 bacterial species and 28 fungal species in the analyzed samples.
- Bacterial species alone accounted for 50% of detections, while fungal species alone represented 6.3%.
- Mixed communities of bacteria and fungi were detected in 43.7% of the samples.
Conclusions:
- DNA sequencing of toenail samples revealed the frequent co-occurrence of bacteria and fungi.
- The findings suggest that mixed microbial communities are prevalent in nail samples.
- Further research is necessary to elucidate the clinical relevance of these mixed communities in nail pathology and to guide treatment strategies.
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