Search bioRxiv⌕ Search

Biology subjects

Alvernaz, S. A.

Publications and source records attributed to Alvernaz, S. A..

2 recordsLinked to original sources

Creation and validation of LIMON - Longitudinal Individual Microbial Omics Networks

Microbial communities are dynamic structures that continually adapt to their surrounding environment. Such communities play pivotal roles in countless ecosystems from environmental to human health. Perturbations of these community structures have been implicated in disease processes such as Crohns disease and cancer. Disturbances to existing ecosystems often occur over time, making it essential to have robust methods for detecting longitudinal alterations in microbial interactions as they develop. Existing methods for identifying temporal microbial community alterations have focused on abundance alterations in individual taxa, rather than relationships between the taxa, known as microbial interactions. Identifying these interactions overtime provides a fuller understanding of how the microbial ecosystem changes as a whole. To fill this gap, we have developed a pipeline that handles the complicated nature of repeated compositional count data, LIMON - Longitudinal Individual Microbial Omics Networks. This novel statistical approach addresses key challenges of modeling temporal and microbial data including overdispersion, zero-inflated count data, compositionality, repeated measure design sample covariates over time, and identification of individualized or sample specific networks. This approach allows users to denoise covariate effects from their data, return networks per time point, identify interaction changes between each time point, and return individual networks and network characteristics per sample/time point. In doing so, LIMON provides a platform to identify the relationship between network interactions and sample features of interest over time. Here we show LIMON, in simulation studies, can accurately remove covariate effects, render sample specific networks, and better recover underlying network edges from covariate confounded data. Analysis of a longitudinal infant microbiome and diet dataset illustrates LIMONs novel utility to identify key microbial interactions related to diet type across time. AUTHOR SUMMARYMicrobes (bacteria, fungi etc.) are integral components of many ecosystems, from the environment to the human body, where they can shift between healthy and disease states. Microbes do not exist alone but in rich diverse communities. Yet, many current methods used to study microbe alterations in disease focus on changes in individual microbes rather than how the entire community adapts. To better understand how microbial communities shift, we developed an open-source tool called LIMON, which allows users study how these relationships shift over time. By leveraging robust statistical techniques, LIMON can account for the complexities of the data, such as covariates and differences between individual samples. This approach helps us uncover important patterns in how microbes interact in various conditions. In this example, we applied LIMON to data from infants who were fed three different diets during the first year of life and identify specific microbial interactions related to diet that change overtime. This work broadens the scope for exploring microbial ecosystem dynamics in health and nature, offering a more comprehensive perspective vs traditional method used.

bioinformatics↗

Suppressed macrophage responses to quorum-sensing-active Streptococcus pyogenes occurs at the level of the nucleus

Streptococcus pyogenes, or Group A Streptococus (GAS), a significant human pathogen, employs quorum sensing (QS) systems to coordinate its behavior and genetic regulation in order to enhance survival. Our previous research established that one such QS system, the Rgg2/3 system, can suppress macrophage NF{kappa}B activity and production of pro-inflammatory cytokines. Yet, the scope of suppression and the mechanism by which it occurs remains unknown. In this study, we used transcriptomic and phosphoproteomic approaches to address these unanswered questions. We found QS-ON GAS broadly suppressed most inflammatory transcriptional pathways including those of NF{kappa}B, type I and type II interferon responses, and intracellular stress responses. Yet, we found no alternative transcriptional programs were activated after QS-ON GAS infection. Additionally, phosphoproteomics showed no disruption in typical inflammatory pathways such as those related to NF{kappa}B and MAPK activation, which was confirmed by western blotting and translocation assays. Instead, the proteomic data highlighted a potential role for epigenetic mechanisms of inflammatory regulation. To determine if epigenetic regulation was involved in QS-mediated immunomodulation, DNA methylation was measured and studies were performed inhibiting various histone and chromatin modifiers. These studies also showed no dijerence between QS-ON compared with QS-OFF infected macrophages. These findings expand our understanding of QS-mediated suppression and of GAS virulence strategies that appear to employ unusual methods of restricting inflammation. Uncovering this mechanism will ojer invaluable insight into GAS, itself, as well as understudied immunological pathways. ImportanceStreptococcus pyogenes is a ubiquitous pathogen that causes over 600 million infections every year and 500 thousand to 1 million fatalities. While in developed countries it is generally known to cause mild conditions such as pharyngitis, it can also manifest as severe infections such as necrotizing fasciitis, septic arthritis, and lead to post-infectious sequelae including rheumatic heart disease and glomerulonephritis. Elucidating new mechanisms of virulence in this organism, including how it evades and suppresses immune responses can be critical in understanding its pathogenicity, epidemiology, and identification of novel treatment avenues in this era of multi-drug-resistant bacteria. In this study, we characterize the broad spectrum by which GAS modulates the host innate immune response and begin to uncover host pathways that bacteria can use or inhibit for its survival.

immunology↗