At PathoSense we use long-read sequencing to analyse the microbiome in the most insightful way. One approach is the amplification of the complete 16S rRNA gene fragment (~1500 bp) so that we can sequence it entirely. This gives advantages for the taxonomical identification with the classification of bacteria up to the species level. Another approach is shotgun metagenomics. Here, DNA is isolated in crude fractions and long strands of bacterial DNA can be used after sequencing to assemble partial and complete bacterial genomes. These assembled metagenomes can be exploited for downstream functional characterisation (see further).

The first insight in the microbial community starts with the members that are there. Using full-length 16S rRNA gene sequencing we can determine bacterial compositions up to genus and species level. Using metagenomic assemblies, we can even go deeper and determine whether specific strains of interest are present in samples.

When metagenomic assemblies are available, we can dig deeper into the functionality of the microbiome. Pathogenic bacteria harbour virulence markers that can be identified with scientifically validated databases. Furthermore, one might be interested to see whether certain treatments affect the presence of antimicrobial resistance gene markers or if certain beneficial genes are found on the contrary. This is state-of-the-art research and we are happy to take you along in this exciting field.

PathoSense collaborates with the LANUPRO laboratory of Ghent University from prof. Jeroen Degroote. A direct measurement of the microbiome's metabolites can be performed to see which concentrations of short-chain fatty acids, lactic acid and ammonia are found. This information can then be linked further to the presence of certain bacteria in the microbial communities.