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Biology subjects

Bari, S. M. N.

Publications and source records attributed to Bari, S. M. N..

2 recordsLinked to original sources

Gene contribution of Streptococcus dysgalactiae subspecies equisimilis, an emerging pathogen, to experimental primate necrotizing myositis

Streptococcus dysgalactiae subspecies equisimilis (SDSE) is an emerging human pathogen closely related to group A streptococcus. However, its genetic requirements for survival and growth in different conditions and for causing invasive infections remain poorly understood. To address this gap, we used Transposon-Directed Insertion-site Sequencing (TraDIS) to identify genes contributing to fitness in experimental necrotizing myositis in non-human primates (NHPs). Using two SDSE stG62647 human clinical isolates, MGCS36044 and MGCS36089, we generated highly saturated transposon mutant libraries and analyzed them following in vitro growth and in vivo infection in eight NHPs. We identified 398 essential genes shared by both strains during growth in vitro and in vivo, and 17 and seven conditionally essential genes required only in vitro or only in vivo, respectively. Additionally, we identified 117 and 110 genes in MGCS36044 and MGCS36089, respectively, that were associated with fitness during necrotizing myositis. Transposon insertions in 34 MGCS36044 genes conferred increased fitness, whereas mutation of 83 genes conferred decreased fitness. Similarly, in MGCS36089, mutations in 38 and 72 genes conferred increased or decreased fitness, respectively. Importantly, both strains shared 46 fitness-associated genes, including an enrichment of transporter genes, highlighting nutrient acquisition as a dominant requirement during infection. The results provide critical information for guiding future translational efforts to develop preventive and therapeutic strategies against human SDSE infections.

microbiology↗

A unique mode of nucleic acid immunity performed by a single multifunctional enzyme

The perpetual arms race between bacteria and their viruses (phages) has given rise to diverse immune systems, including restriction-modification and CRISPR-Cas, which sense and degrade phage-derived nucleic acids. These complex systems rely upon production and maintenance of multiple components to achieve anti-phage defense. However, the prevalence and effectiveness of much simpler, single-component systems that cleave DNA remain unknown. Here, we describe a novel mode of nucleic acid immunity performed by a single enzyme with nuclease and helicase activities, herein referred to as Nhi. This enzyme provides robust protection against diverse staphylococcal phages and prevents phage DNA accumulation in cells stripped of all other known defenses. Our observations support a model in which Nhi acts as both the sensor and effector to degrade phage-specific replication intermediates. Importantly, Nhi homologs are distributed in diverse bacteria and exhibit functional conservation, highlighting the versatility of such compact weapons as major players in anti-phage defense.

microbiology↗