Abstract
The human microbiome can play key roles in disease, and diagnostic testing will soon have the ability to examine these roles in the context of clinical applications. Currently, most diagnostic testing in pathology applications focuses on a small number of disease‐causing microbes and dismisses the whole microbial community that causes or is modulated by disease. Microbiome modifications have already provided clinically relevant insights in gut and oral diseases, such as irritable bowel disease, but there are currently limitations when clinically examining microbiomes outside of these body sites. This is critical, as the majority of microbial samples used in pathology originate from body sites that contain low concentrations of microbial DNA, including skin, tissue, blood, and urine. These samples, also known as low microbial biomass samples, are difficult to examine without careful consideration and precautions to mitigate contamination and biases. Here, we present the limitations when analysing low microbial biomass samples using current protocols and techniques and highlight the advantages that microbiome testing can offer diagnostics in the future, if the proper precautions are implemented. Specifically, we discuss the sources of contamination and biases that may result in false assessments for these sample types. Finally, we provide recommendations to mitigate contamination and biases from low microbial biomass samples during diagnostic testing, which will be especially important to effectively diagnose and treat patients using microbiome analyses.
Highlights
Existing pathology techniques currently survey small numbers of disease-causing microbes by applying Koch’s postulates
Diagnostic testing is typically limited to one potential pathogen per test; several diseases can manifest as co-infections or poly-microbial infections, where multiple microorganisms contribute to the disease
The microbiome will become an important asset for diagnostics and treating human diseases
Summary
Existing pathology techniques currently survey small numbers of disease-causing microbes by applying Koch’s postulates. J Pathol Clin Res April 2020 6: 97–106 sequencing approaches) [25] These approaches can aid in the identification, function, and activity levels of known and novel species/strains that contribute to infectious diseases [4,26,27], which is important for diagnosis and treatment, and critical for the downstream development of new rapid and cost effective techniques to readily detect these pathogens. The human microbiome typically contributes over 3 million genes in every single human, which is approximately 150 times more genes than the human genome [28] This volume of information is not routinely assessed in current diagnostic testing and could inform more effective treatment strategies or identify unknown infection dynamics. We discuss in detail how microbiome testing can provide additional information when diagnosing communicable and noncommunicable diseases in the future
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