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Title: | High hemolytic activity of the Staphylococcus aureus spa t1081 among clonal complex 45 in Taiwan |
Authors: | Lin, Yu-Tzu Lee, Chun-Li Lin, Chin-Yun Lee, Tai-Fen Hsueh, Po-Ren |
Keywords: | CC45 t1081 Blood culture MLVA Hemolytic activity |
Issue Date: | Aug-2024 |
Publisher: | Journal of Microbiology, Immunology and Infection |
Citation: | Original Article |
Abstract: | Abstract Background: Methicillin-resistant Staphylococcus aureus (MRSA) sequence type (ST) 45 was first reported in Taiwan in 2006. Since then, the prevalence of ST45 MRSA in clinical isolates has increased. This study was carried out to understand the changes in the proportions, evolutionary relationships, and infection advantages of ST45 and its related clones. Materials and methods: S. aureus including MRSA and MSSA (methicillin-sensitive S. aureus), and clonal complex (CC) 45 blood isolates were collected in 2000, 2005, and from January 2010 to August 2014. Molecular typing, multiple-locus variable-number tandem repeat analysis (MLVA) and single nucleotide polymorphism (SNP)-based phylogenetic analysis were performed. Fitness and virulence analyses were used to understand the infection advantages of the isolates. Results: Among the 67 CC45 isolates, only MSSA ST508 isolates were found in 2000 and 2005. Since 2010, the prevalence of MRSA has increased, t1081/ST45 has become dominant, and MRSA ST508 has been found. Phylogenetic analysis indicated that most of the ST45 isolates were located in a cluster distinct from those of ST508 and ST929. However, the t026 isolates clustered with the ST508 isolates rather than with the other ST45 isolates. Moreover, fitness and virulence analyses revealed that the t1081 isolates had higher hemolytic activity than the t026 and ST508 isolates did. |
URI: | http://localhost:8080/xmlui/handle/123456789/9716 |
Appears in Collections: | Vol 57 No 6 (2024) |
Files in This Item:
File | Description | Size | Format | |
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High-hemolytic-activity-of-the-Staphylococcus-a_2024_Journal-of-Microbiology.pdf | 1.3 MB | Adobe PDF | View/Open |
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