-
Je něco špatně v tomto záznamu ?
Investigation of biofilm formation in methicillin-resistant Staphylococcus aureus associated with bacteraemia in a tertiary hospital
WK. Niek, CSJ. Teh, N. Idris, KL. Thong, ST. Ngoi, SSS. Ponnampalavanar
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
FP016-2014B
Ministry of Higher Education Fundamental Research Grant Scheme (FRGS)</
IF004-2020
International Research Funding
- MeSH
- bakteriemie * mikrobiologie MeSH
- biofilmy * MeSH
- centra terciární péče MeSH
- lidé MeSH
- methicilin rezistentní Staphylococcus aureus * fyziologie MeSH
- stafylokokové infekce * mikrobiologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Biofilm formation is an important physiological process in Staphylococcus aureus (S. aureus) that can cause infections in humans. In this study, the ability of 36 methicillin-resistant S. aureus (MRSA) clinical isolates to form biofilm was studied based on genotypic and phenotypic approaches. These isolates were genotyped based on the microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) and biofilm-associated genes (icaAD) via polymerase chain reactions. Phenotyping was performed based on the determination of the strength of biofilm formation of MRSA isolates in vitro. The most prevalent MSCRAMMs and biofilm-associated genes were clfA, eno, and icaD, followed by clfB. The fnbB (38.9%) and ebpS (11.1%) occurred less frequently among the MRSA isolates, while bbp and fnbA genes were absent from all isolates. The MRSA isolates were mostly moderate to strong biofilm formers, despite the heterogeneity of the MSCRAMM profiles. MRSA isolates from different infection sources (primary, catheter-related bloodstream, or secondary infections) were capable of forming strong biofilms. However, persistent bacteraemia was observed only in 19.4% of the MRSA-infected individuals. This study suggested that persistent MRSA bacteraemia in patients might not be associated with the biofilm-forming ability of the isolates.
Department of Medical Microbiology Faculty of Medicine Universiti Malaya 50603 Kuala Lumpur Malaysia
Department of Medicine Faculty of Medicine Universiti Malaya 50603 Kuala Lumpur Malaysia
Nanotechnology and Catalysis Research Centre Universiti Malaya 50603 Kuala Lumpur Malaysia
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21029482
- 003
- CZ-PrNML
- 005
- 20211206103720.0
- 007
- ta
- 008
- 211206s2021 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12223-021-00877-x $2 doi
- 035 __
- $a (PubMed)34089493
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Niek, Wen Kiong $u Department of Medical Microbiology, Faculty of Medicine, Universiti Malaya, 50603, Kuala Lumpur, Malaysia
- 245 10
- $a Investigation of biofilm formation in methicillin-resistant Staphylococcus aureus associated with bacteraemia in a tertiary hospital / $c WK. Niek, CSJ. Teh, N. Idris, KL. Thong, ST. Ngoi, SSS. Ponnampalavanar
- 520 9_
- $a Biofilm formation is an important physiological process in Staphylococcus aureus (S. aureus) that can cause infections in humans. In this study, the ability of 36 methicillin-resistant S. aureus (MRSA) clinical isolates to form biofilm was studied based on genotypic and phenotypic approaches. These isolates were genotyped based on the microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) and biofilm-associated genes (icaAD) via polymerase chain reactions. Phenotyping was performed based on the determination of the strength of biofilm formation of MRSA isolates in vitro. The most prevalent MSCRAMMs and biofilm-associated genes were clfA, eno, and icaD, followed by clfB. The fnbB (38.9%) and ebpS (11.1%) occurred less frequently among the MRSA isolates, while bbp and fnbA genes were absent from all isolates. The MRSA isolates were mostly moderate to strong biofilm formers, despite the heterogeneity of the MSCRAMM profiles. MRSA isolates from different infection sources (primary, catheter-related bloodstream, or secondary infections) were capable of forming strong biofilms. However, persistent bacteraemia was observed only in 19.4% of the MRSA-infected individuals. This study suggested that persistent MRSA bacteraemia in patients might not be associated with the biofilm-forming ability of the isolates.
- 650 12
- $a bakteriemie $x mikrobiologie $7 D016470
- 650 12
- $a biofilmy $7 D018441
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a methicilin rezistentní Staphylococcus aureus $x fyziologie $7 D055624
- 650 12
- $a stafylokokové infekce $x mikrobiologie $7 D013203
- 650 _2
- $a centra terciární péče $7 D062606
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Teh, Cindy Shuan Ju $u Department of Medical Microbiology, Faculty of Medicine, Universiti Malaya, 50603, Kuala Lumpur, Malaysia
- 700 1_
- $a Idris, Nuryana $u Department of Medical Microbiology, Faculty of Medicine, Universiti Malaya, 50603, Kuala Lumpur, Malaysia
- 700 1_
- $a Thong, Kwai Lin $u Nanotechnology & Catalysis Research Centre (NANOCAT), Universiti Malaya, 50603, Kuala Lumpur, Malaysia
- 700 1_
- $a Ngoi, Soo Tein $u Department of Medical Microbiology, Faculty of Medicine, Universiti Malaya, 50603, Kuala Lumpur, Malaysia
- 700 1_
- $a Ponnampalavanar, Sasheela Sri La Sri $u Department of Medicine, Faculty of Medicine, Universiti Malaya, 50603, Kuala Lumpur, Malaysia. sheela@ummc.edu.my
- 773 0_
- $w MED00011005 $t Folia microbiologica $x 1874-9356 $g Roč. 66, č. 5 (2021), s. 741-749
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34089493 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211206 $b ABA008
- 991 __
- $a 20211206103717 $b ABA008
- 999 __
- $a ok $b bmc $g 1731482 $s 1150035
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 66 $c 5 $d 741-749 $e 20210605 $i 1874-9356 $m Folia microbiologica $n Folia microbiol. (Prague) $x MED00011005
- GRA __
- $a FP016-2014B $p Ministry of Higher Education Fundamental Research Grant Scheme (FRGS)</
- GRA __
- $a IF004-2020 $p International Research Funding
- LZP __
- $a Pubmed-20211206