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Oral Biofilm Sampling for Microbiome Analysis in Healthy Children
Published on: December 31, 2017
Examining the Evidence for an Adult Healthy Middle Ear Microbiome
Jake Jervis-Bardy1,2, Lex E X Leong3,4, Lito E Papanicolas3,4
1Department of Otolaryngology-Head & Neck Surgery, Flinders Medical Centre, College of Medicine and Public Health, Flinders University, Adelaide, South Australia, Australia jakejervisbardy@hotmail.com.
Abstract:
Otitis media (OM) is a cluster of diseases of the middle ear that commonly result from bacterial infection. OM subtypes in which the tympanic membrane is intact (acute otitis media and otitis media with effusion) are presumed to result from pathogen translocation through the eustachian tube. Recent molecular-based studies have suggested that a diverse middle ear microbiome exists in the absence of disease. These have been largely unsupported by culture and feature species that commonly contaminate low-biomass sequencing data. Combining culture-based and molecular techniques, we undertook a detailed investigation of the evidence for bacterial colonization of the healthy middle ear. Middle ear (ME), nasopharynx (NP), and external ear canal (EC) swabs were collected from a total of 25 adult patients undergoing cochlear implant, stapedotomy, or translabyrinthine vestibular schwannoma resection. Diagnostic culture, microscopy, quantitative PCR, and 16S rRNA gene amplicon sequencing were used to assess sample bacterial content. EC and NP microbiota were consistent with previous reports. In contrast, bacterial levels in ME samples were not significantly above those in unused control swabs. Commonly detected taxa were among recognized sequencing contaminants (Methylobacterium, Pseudomonas, and Acinetobacter). Linear regression of dominant ME taxa confirmed a negative relationship between relative abundance and bacterial load, consistent with contamination. No bacteria were detected by microscopy or diagnostic culture in any middle ear sample. Our findings cast substantial doubt on previous reports identifying a healthy middle ear microbiome using 16S amplicon sequencing.IMPORTANCE Recent molecular-based studies have suggested that a diverse middle ear microbiome in adults and children can exist in the absence of disease. These studies have been largely unsupported by culture and feature species that commonly contaminate low-biomass sequencing data. While 16S rRNA gene amplicon sequencing has proven to be a highly informative technique in many clinical contexts, it is susceptible to spurious signal arising from sequencing reagent contaminants where sample biomass is low. Combining culture-based and molecular techniques, we undertook a detailed investigation of the evidence for bacterial colonization of the healthy middle ear. In finding no evidence of viable bacterial cells in middle ear samples, our study further underlines the importance of careful consideration of amplicon sequence data derived from very-low-biomass contexts and the value of analytical approaches that combine culture and molecular techniques.
Insights
This study found no evidence of bacteria in healthy adult middle ears, challenging previous molecular findings. Combining culture and molecular methods, researchers suggest common sequencing contaminants may explain prior microbiome reports.
Area of Science:
- Microbiology
- Otolaryngology
- Genomics
Background:
- Otitis media (OM) is a common middle ear disease often linked to bacterial infection.
- Previous molecular studies suggested a healthy middle ear microbiome, but lacked robust validation.
- Low-biomass samples are susceptible to contamination in molecular sequencing, potentially skewing results.
Purpose of the Study:
- To investigate the presence of bacterial colonization in the healthy adult middle ear.
- To reconcile discrepancies between culture-based and molecular findings regarding the middle ear microbiome.
- To assess the validity of previous molecular studies on the healthy middle ear microbiome.
Main Methods:
- Collected middle ear (ME), nasopharynx (NP), and external ear canal (EC) swabs from 25 adult patients.
- Employed diagnostic culture, microscopy, quantitative PCR, and 16S rRNA gene amplicon sequencing.
- Compared ME bacterial levels against unused control swabs and analyzed dominant taxa.
Main Results:
- No bacteria were detected in ME samples via microscopy or diagnostic culture.
- Bacterial levels in ME samples were not significantly higher than in unused control swabs.
- Detected taxa in ME samples were consistent with known sequencing contaminants.
Conclusions:
- Findings cast substantial doubt on previous reports of a healthy middle ear microbiome.
- The study highlights the importance of rigorous methods, including culture, for low-biomass samples.
- Contamination is a likely explanation for previously reported diverse middle ear microbiomes.
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