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      Emergence of Panton-Valentine leukocidin-positive ST59 methicillin-susceptible Staphylococcus aureus with high cytolytic peptide expression in association with community-acquired pediatric osteomyelitis complicated by pulmonary embolism.

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          Abstract

          A 15-year-old boy, who had had a furuncle on his femur, developed femoral pyomyositis and osteomyelitis complicated by septic pulmonary embolism. Panton-Valentine leukocidin-positive (PVL(+)) ST59 methicillin-susceptible Staphylococcus aureus (MSSA) was isolated from pus and blood. Chemotherapy was started with cefazolin, followed by combination therapy with meropenem/vancomycin with surgery. The MSSA (strain KS1) was positive for increased levels of cytolytic peptide (psmα and hld) and staphylococcal enterotoxin B (SEB), and manifested IS1216V-mediated multidrug resistance (to erythromycin, clindamycin, kanamycin, streptomycin, and chloramphenicol), similar to a genome-analyzed reference strain (PM1) of ST59/SCCmecV(5C2&5) community-associated methicillin-resistant S. aureus (Taiwan CA-MRSA), but unlike another reference strain (M013) of Taiwan CA-MRSA in terms of resistance. The data suggest that CA-MSSA KS1, characterized by PVL, increased levels of cytolytic peptide, SEB, and multidrug resistance, is a possible ancestral strain of Taiwan CA-MRSA and causes the unique association of osteomyelitis and septic pulmonary embolism, requiring complicated management.

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          Author and article information

          Journal
          J Microbiol Immunol Infect
          Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi
          1995-9133
          1684-1182
          Oct 2015
          : 48
          : 5
          Affiliations
          [1 ] Department of Pediatrics, Kofu Municipal Hospital, Kofu, Japan.
          [2 ] Department of Clinical Laboratory Sciences and Medical Biotechnology, National Taiwan University College of Medicine, Taipei, Taiwan; Division of Bacteriology, Department of Infectious Disease Control and International Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
          [3 ] Division of Bacteriology, Department of Infectious Disease Control and International Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
          [4 ] Department of Orthopedic Surgery, Kofu Municipal Hospital, Kofu, Japan.
          [5 ] Division of Endocrinology and Metabolism, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
          [6 ] Division of Bacteriology, Department of Infectious Disease Control and International Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; International Medical Education and Research Center, Niigata, Japan.
          [7 ] International Medical Education and Research Center, Niigata, Japan.
          [8 ] Department of Clinical Laboratory Sciences and Medical Biotechnology, National Taiwan University College of Medicine, Taipei, Taiwan.
          [9 ] Division of Bacteriology, Department of Infectious Disease Control and International Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; International Medical Education and Research Center, Niigata, Japan. Electronic address: tatsuoy@imerc.jp.
          Article
          S1684-1182(14)00111-X
          10.1016/j.jmii.2014.04.015
          25070278
          8c3754fa-b98a-4ac8-98a7-4c1a8d6d48fc
          Copyright © 2014. Published by Elsevier B.V.
          History

          antibiotic treatment,community-associated methicillin-susceptible Staphylococcus aureus (CA-MSSA),genotype,pediatric osteomyelitis,septic pulmonary embolism

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