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Iosifidis, G.

Publications and source records attributed to Iosifidis, G..

2 recordsLinked to original sources

Social network cycle motifs and gut microbiome strain-sharing

Microbes are commonly transmitted through human social interactions, yet little is known about how higher-order social network structures shape microbial circulation. Here, we analyze network cycles, i.e., closed loops of individuals, in both friendship networks and microbial networks, across 1,787 individuals from 18 isolated Honduran villages. Using strain-level resolution, we construct species-specific microbial networks, study their cyclic structure, and compare them with the social networks in the same population. Cycles were strongly over-represented relative to degree-preserving randomized networks in both social and microbial networks for most species, indicating that microbial transmission frequently occurs within recurrent and clustered groups of hosts. However, the overlap between microbial and social cycles varies substantially across species and individuals, and regression analyses identify a small subset of species whose cyclic sharing patterns are associated with social cycle participation. Notably, several anaerobic species show negative associations, suggesting reliance on repeated local exposures or shared environments only partially aligned with social ties. Consistent with this, many species exhibit niche-like transmission pathways independent of social network structure. Together, these findings show that microbial sharing networks exhibit rich higher-order organization that only partially mirrors human social networks and that reveals that network cycles can provide a useful framework for understanding how repeated exposure might contribute to microbial spread.

microbiology↗

The role of bacterial size, shape and surface in macrophage engulfment of uropathogenic E. coli cells

Uropathogenic Escherichia coli (UPEC) can undergo extensive filamentation in the host during acute urinary tract infections (UTIs). It has been hypothesised that this morphological plasticity allows bacteria to avoid host immune responses such as macrophage engulfment. However, it is still unclear what properties of filaments are important in macrophage-bacteria interactions. The aim of this work was to investigate the contribution of bacterial biophysical parameters, such as cell size and shape, and physiological parameters, such as cell surface and the environment, to macrophage engulfment efficiency. Viable, reversible filaments of known lengths and volumes were produced in the UPEC strain UTI89 using a variety of methods, including exposure to cell-wall targeting antibiotics, genetic manipulation and isolation from an in vitro human bladder cell model. Quantification of the engulfment ability of macrophages using gentamicin-protection assays and fluorescence microscopy demonstrated that the ability of filaments to avoid macrophage engulfment is dependent on a combination of size (length and volume), shape, surface and external environmental factors. UTI89 filamentation was also found to occur independently of the SOS-inducible filamentation genes, sulA and ymfM, demonstrating the non-essential requirement of these genes for UTI89 filamentation and their ability to avoid macrophage engulfment. With several strains of UPEC now resistant to current antibiotics, our work identifies the importance of bacterial morphology during infection and may provide new ways to prevent or treat these infections via immune modulation or antimicrobials. Author SummaryUrinary tract infections (UTIs) are one of the most common bacterial infections worldwide with 50% of women suffering from a UTI during their lifetime. Escherichia coli is the primary bacteria responsible for UTIs and is usually found in short rod forms. However, during UTIs E. coli can elongate into extremely long thin shapes called filaments. Filaments are thought to be advantageous during infections because they are too long to be engulfed and killed by immune cells called macrophages. Due to increasing antibiotic resistance in bacteria there is a strong need for the discovery of new ways to treat infections and this is only possible once we thoroughly understand the mechanisms bacteria employ to overcome our immune response. Therefore, we investigated the effect of E. coli filamentation on macrophage engulfment along with other aspects of bacteria reported to influence engulfment. We found that the ability of filaments to avoid macrophage engulfment is dependent on a combination of size (length and volume), shape, surface and external environmental factors. Our research has highlighted the importance of bacterial shape changes during infections and provided a foundational understanding of macrophage engulfment of filaments. Eventually, this knowledge may reveal new targets for treatment of infections.

microbiology↗