Streptococcal toxic shock syndrome (STSS) is a severe invasive infection characterized by the sudden onset of shock, multiorgan failure, and high mortality. Although STSS is mainly caused by Streptococcus pyogenes, group G streptococcus identified as S. dysgalactiae subsp. equisimilis (SDSE) causing STSS has also been reported; however, no study has analyzed >100 isolates of SDSE causing STSS. Therefore, we characterized the emm genotype of 173 SDSE isolates obtained from STSS patients in Japan during 2014-2016 and performed antimicrobial susceptibility testing using the broth microdilution method and emm gene typing. The predominant emm genotype was found to be stG6792, followed by stG485, stG245, stG10, stG6, and stG2078. These six genotypes constituted more than 75% of the STSS isolates. The proportion of each emm genotype in STSS isolates correlated with that in invasive isolates previously reported. We found that 16.2% of the isolates showed clindamycin resistance. The proportion of clindamycin-resistant SDSE isolates was significantly higher than that of S. pyogenes isolates. Thus, while treating STSS caused by SDSE, it is necessary to consider the possibility of clindamycin resistance and to ensure judicious use of the drug.
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http://dx.doi.org/10.1016/j.jiac.2017.09.013 | DOI Listing |
Neurology
October 2024
From the MS Center Amsterdam (F.C.L., E.M.M.S., B.U.), Neurology, Amsterdam Neuroscience, Genomics of Neurodegenerative Diseases and Aging (D.Á.S., N.T., H.H., A.N.S., M.H., S.J.V.D.L.), Human Genetics, and Alzheimer Center Amsterdam (H.H., S.J.V.D.L.), Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc; Delft Bioinformatics Lab (N.T., H.H.), Delft University of Technology; and Amsterdam Neuroscience (H.H., S.J.V.D.L.), Neurodegeneration, the Netherlands.
Background And Objectives: More than 200 genetic variants have been associated with multiple sclerosis (MS) susceptibility. However, it is unclear to what extent genetic factors influence lifetime risk of MS. Using a population-based birth-year cohort, we investigate the effect of genetics on lifetime risk of MS.
View Article and Find Full Text PDFJ Infect Dis
August 2024
UQ Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
J Clin Microbiol
October 2024
Department of Medical Microbiology and Infection Prevention, Amsterdam UMC location University of Amsterdam, Amsterdam, the Netherlands.
Since 2022, many countries have reported an upsurge in invasive group A streptococcal (iGAS) infections. We explored whether changes in carriage rates or emergence of strains with potentially altered virulence, such as 1 variants M1 and M1, contributed to the 2022/2023 surge in the Netherlands. We determined (sub)type distribution for 2,698 invasive and 351 .
View Article and Find Full Text PDFMicrob Genom
August 2024
The Florey Institute of Infection, University of Sheffield, Sheffield, UK.
Myocarditis is clinically characterized by chest pain, arrhythmias, and heart failure, and treatment is often supportive. Mutations in DSP, a gene encoding the desmosomal protein desmoplakin, have been increasingly implicated in myocarditis. To model DSP-associated myocarditis and assess the role of innate immunity, we generated engineered heart tissues (EHTs) using human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) from patients with heterozygous DSP truncating variants (DSPtvs) and a gene-edited homozygous deletion cell line (DSP-/-).
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