Rhodococcus spp. interacts with human norovirus in clinical samples and impairs its replication on human intestinal enteroids

Viral infections, particularly human norovirus (NoV), are a leading cause of diarrheal diseases globally. To better understand NoV susceptibility, it is crucial to investigate both host glycobiology and the influence of the microbiota. Histo-blood group antigens (HBGA) displayed on surfaces of host cells act as NoV receptors, while certain bacteria express HBGA-like substances, facilitating virus-bacteria interactions. To identify bacterial species interacting with NoV during infection, stool samples from children infected with NoV GII.4 were analyzed. The samples were subjected to bacteria separation using anti-NoV GII.4 polyclonal antibodies coupled to magnetic beads, followed by microbiota profiling through 16S rDNA sequencing. This approach identified the genus Rhodococcus as enriched in samples captured with anti-NoV antibodies compared to controls. Electron microscopy confirmed the binding of NoV GII.4 Sydney 2012 viral-like particles (VLP) to five Rhodococcus strains from different species, which expressed HBGA-like substances on their surfaces, particularly from A and B blood groups. In human intestinal enteroids, Rhodococcus erythropolis reduced NoV GII.4 Sydney 2012 infection levels under displacement, exclusion and competitive exclusion settings. Extracellular polysaccharides (EPS) isolated from Rhodococcus strains bound VLP from both GII.4 and GII.6 genotypes. Blocking antibodies targeting A and B epitopes reduced the binding of the EPS from R. erythropolis to GII.6 VLP, while enhanced binding to GII.4 VLP was observed when A and B epitopes were blocked. These findings revealed the interaction of Rhodococcus to NoV in an in vitro setting and open new avenues for developing innovative antiviral strategies to prevent and treat NoV infections through the HBGA-like substances present in their EPS.

This work was supported by the Spanish Ministry of Science and Innovation (MICIN)/Spanish State Research Agency (AEI)/10.13039/501100011033 under Grant [PID2020-115403RB-C21] to M.J.Y., PID2020-115403RB-C22 to J.R.-D., and PID2019-105509RJ-I00 to W.R. The study was also supported by Valencian Government grant AICO/2021/033 to J.R.-D. C.S.-B. and S.L.-N. are recipients of the FPI PRE2018-083315 and FPU22/00443 predoctoral grants by MICIN/AEI/10.13039/501100011033 and by “ESF Investing in your future”. N.P.-G., R.C.-C., and N.N.-L. are recipients of predoctoral grants from the Valencian Government (ACIF/2020/085, CIACIF/2021/162 and ACIF/2020/076).

Peer reviewed