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耐甲氧西林金黄色葡萄球菌分子流行病学变化对血流感染严重程度和死亡率的长期影响。

Long-term impact of molecular epidemiology shifts of methicillin-resistant on severity and mortality of bloodstream infection.

作者信息

Kaku Norihito, Ishige Masaki, Yasutake Go, Sasaki Daisuke, Ota Kenji, Mitsumoto-Kaseida Fujiko, Kosai Kosuke, Hasegawa Hiroo, Izumikawa Koichi, Mukae Hiroshi, Yanagihara Katsunori

机构信息

Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.

出版信息

Emerg Microbes Infect. 2025 Dec;14(1):2449085. doi: 10.1080/22221751.2024.2449085. Epub 2025 Jan 9.

DOI:10.1080/22221751.2024.2449085
PMID:39789882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11727054/
Abstract

A 2019 nationwide study in Japan revealed the predominant methicillin-resistant Staphylococcus aureus (MRSA) types in bloodstream infections (BSIs) to be sequence type (ST)8-carrying SCC type IV (ST8-MRSA-IV) and clonal complex 1-carrying SCC type IV (CC1-MRSA-IV). However, detailed patient characteristics and how these MRSA types evolve over time remain largely unknown. In this long-term single-center study, MRSA strains isolated from blood cultures at Nagasaki University Hospital from 2012 to 2019 were sequenced and analyzed. Additionally, we compared the SCC types and patient characteristics identified in this study with previous data from our hospital spanning 2003-2007 and 2008-2011. Over this 16-year period, SCC type II decreased significantly from 79.2% to 15.5%, while type IV increased from 18.2% to 65.5%. This shift in SCC types was associated with notable changes in severity and outcomes; the sequential organ failure assessment (SOFA) score decreased from 5.8 to 3.1; in-hospital mortality declined from 39.8% to 15.5%. In contrast, no significant changes in patient demographics, such as age, sex, or underlying diseases, were observed. Between 2012 and 2019, the major combinations of SCC type and sequence type were ST8-MRSA-IV, ST8-MRSA-I, CC1-MRSA-IV, and ST5-MRSA-II. Additionally, ST8-MRSA-IV was divided into CA-MRSA/J, t5071-ST8-MRSA-IV, and USA300-like clone based on the results of molecular analysis. These major combinations showed similar drug resistance patterns, molecular characteristics, and phylogenetic features to those identified in nationwide surveillance. This study highlights the evolving nature of MRSA types in bloodstream infections, correlating with improved patient outcomes over time.

摘要

2019年在日本开展的一项全国性研究显示,血流感染(BSI)中占主导地位的耐甲氧西林金黄色葡萄球菌(MRSA)类型为携带IV型葡萄球菌盒式染色体(SCC)的序列型(ST)8(ST8-MRSA-IV)和携带IV型SCC的克隆复合体1(CC1-MRSA-IV)。然而,详细的患者特征以及这些MRSA类型如何随时间演变在很大程度上仍不清楚。在这项长期的单中心研究中,对2012年至2019年长崎大学医院从血培养中分离出的MRSA菌株进行了测序和分析。此外,我们将本研究中确定的SCC类型和患者特征与我院2003 - 2007年和2008 - 2011年的先前数据进行了比较。在这16年期间,II型SCC从79.2%显著下降至15.5%,而IV型从18.2%增加至65.5%。SCC类型的这种转变与严重程度和结局的显著变化相关;序贯器官衰竭评估(SOFA)评分从5.8降至3.1;住院死亡率从39.8%降至15.5%。相比之下,未观察到患者人口统计学特征(如年龄、性别或基础疾病)的显著变化。2012年至2019年期间,SCC类型和序列类型的主要组合为ST8-MRSA-IV、ST8-MRSA-I、CC1-MRSA-IV和ST5-MRSA-II。此外,根据分子分析结果,ST8-MRSA-IV被分为社区获得性MRSA/J、t5071-ST8-MRSA-IV和USA300样克隆。这些主要组合显示出与全国监测中确定的耐药模式、分子特征和系统发育特征相似。本研究突出了血流感染中MRSA类型的演变性质,与患者结局随时间的改善相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/f7a622298f6f/TEMI_A_2449085_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/24430f971fdc/TEMI_A_2449085_F0001_OB.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/8223d70e21d5/TEMI_A_2449085_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/166bdfe888a1/TEMI_A_2449085_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/4d034fae9360/TEMI_A_2449085_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/f7a622298f6f/TEMI_A_2449085_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/24430f971fdc/TEMI_A_2449085_F0001_OB.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/8223d70e21d5/TEMI_A_2449085_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/166bdfe888a1/TEMI_A_2449085_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/4d034fae9360/TEMI_A_2449085_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d1/11727054/f7a622298f6f/TEMI_A_2449085_F0005_OC.jpg

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