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Alshaya, D. S.

Publications and source records attributed to Alshaya, D. S..

2 recordsLinked to original sources

Comparative Genome Study of Multidrug-resistant Serratia marcescens strain IU-BTGE-M-3 Isolated from a Diarrheal Patient Reveals Antibiotic Resistance Profile

Serratia marcescens is a notable pathogen known for its intrinsic and acquired antimicrobial resistance, posing challenges in healthcare. The study investigates the multidrug-resistant (MDR) Serratia marcescens strain BTGE-M-3, focusing on its genomic features and antibiotic resistance. The strain was identified using both morphological and molecular approaches, and its genome, which measured 4.97 Mbp and exhibited a GC content of 59.7%, was sequenced. The genome has 4,827 genes, including essential antibiotic resistance genes, such as tet (41) for tetracyclines, aac (6')-Ic for aminoglycosides, OqxB for fluoroquinolones, and blaSST-1 beta-lactam, alongside various virulence determinants. Comparative genomics revealed high similarity (98.06% ANI) to S. marcescens strain KS10, supporting its classification within the same species. Additionally, the genome analysis showed that S. marcescens strain IU-BTGE-M-3 comprises of 4390 gene clusters, 4564 genes, and 244 unique singleton genes. To summarize, the results showed that S. marcescens strain IU-BTGE-M-3 exhibited a high level of genomic diversity as well as diverse metabolic, cellular, and biological functions, and it is hypothesized that frequent strain exchanges resulted in the horizontal transfer of drug resistance genes. This study underscores the importance of genomic surveillance in understanding and combating antibiotic resistance in therapeutic settings.

genomics↗

Deciphering Immune Complexity: Single-Cell Insights into Autoimmune Myocarditis Progression

Autoimmune myocarditis is a complex inflammatory response in the heart caused by abnormal immune system activity. We used modern single-cell technologies to analyze the complex gene expression patterns in autoimmune myocarditis tissue samples during several stages of inflammation: acute, subacute, and chronic. We identified the presence of T cell-monocyte complexes in both control and myocarditis samples from different phases using detailed analysis of vast single-cell RNA sequencing data. These complexes were notably more prevalent throughout the acute and subacute stages. Our investigation of gene ontology revealed their involvement in important processes as signal transduction, immune response control, and T cell proliferation and activation. We conducted a thorough analysis of trajectories, uncovering the step-by-step changes of macrophages into clusters linked to antigen presentation, oxidative stress responses, complement activation, and phagocytosis. Furthermore, our examination of neutrophil paths revealed their development and maturation from the bone marrow to distinct functional stages. Our analysis of cellular communication networks revealed consistent and phase-specific patterns, providing valuable information on how immune responses change as the disease progresses. We noted a substantial increase in BAFF signaling from normal to acute phases, while CHEMERIN signaling was upregulated from acute to chronic phases. The discoveries greatly improve our understanding of autoimmune myocarditis on a molecular level, providing a strong basis for creating personalized precision medicine treatments for each patient. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=141 SRC="FIGDIR/small/584698v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@1150607org.highwire.dtl.DTLVardef@13eb725org.highwire.dtl.DTLVardef@6a0be9org.highwire.dtl.DTLVardef@3400ac_HPS_FORMAT_FIGEXP M_FIG C_FIG

genomics↗