scholarly journals Molecular characterization of the gene encoding high-level mupirocin resistance in Staphylococcus aureus J2870.

1994 ◽  
Vol 38 (5) ◽  
pp. 1205-1208 ◽  
Author(s):  
J E Hodgson ◽  
S P Curnock ◽  
K G Dyke ◽  
R Morris ◽  
D R Sylvester ◽  
...  
2015 ◽  
Vol 53 (11) ◽  
pp. 3699-3701 ◽  
Author(s):  
Jeanette W. P. Teo ◽  
Steven Kum ◽  
Roland Jureen ◽  
Raymond T. P. Lin

Here we report a catalase-negative methicillin-sensitiveStaphylococcus aureusisolate collected from a blood culture. Sequencing through the gene encoding catalase,katA, demonstrated a 2-bp insertion. The resulting frameshift mutation generates a protein that has lost 26 amino acids (aa) at its C-terminal domain.


2012 ◽  
Vol 51 (3) ◽  
pp. 1005-1007 ◽  
Author(s):  
Krešimir Matanović ◽  
Eduardo Pérez-Roth ◽  
Selma Pintarić ◽  
Branka Šeol Martinec

2020 ◽  
Vol 29 (3) ◽  
pp. 171-177
Author(s):  
Marwa S. Mostaf ◽  
Alaa R. Awad

Background: Two types of mupirocin resistance among methicillin resistant Staphylococcus aureus (MRSA) have been reported; low-level mupirocin resistance (LL-MR), and high-level mupirocin resistance (HL-MR). The mupA gene is typically located on mobile genetic elements which facilitate the resistance dissemination. Objective: The aim of this work was to identify the mupA gene location, as well as the restriction fragment length polymorphism (RFLP) patterns in high and low-level mupirocin resistant MRSA. Methodology: This study was conducted on 100 MRSA isolates; seven of them were mupirocin resistant. The E test was used to identify high and low level mupirocin resistance. Amplification of mupA gene in total and plasmid DNA was performed. We also detected the spacer region (trsLM–IS257-like–mupA) in the 7 isolates by PCR then we investigated its RFLP patterns. Results: Four MR MRSA isolates had low level resistance, their MupA gene was located on chromosomal DNA, whereas, three isolates showed high level MR, their MupA gene was located on plasmid DNA. Four types of different RFLP patterns of the spacer region were identified; type-1 included two LL-MR isolates, each of type-2 and 3 included both HL-MR and LL-MR isolates, and type-4 included one HL-MR isolate. Conclusions: Staphylococcus aureus mupA gene responsible for LL-MR is located on the chromosome while that responsible for HL-MR is plasmid-mediated. The spacer region variations appear to occur in both chromosomal and plasmid-located mupA gene regardless the type of mupirocin resistance.


2021 ◽  
pp. 109160
Author(s):  
Magdalena Kizerwetter-Świda ◽  
Dorota Chrobak-Chmiel ◽  
Ewelina Kwiecień ◽  
Magdalena Rzewuska ◽  
Marian Binek

Author(s):  
Fatima N. Aziz ◽  
Laith Abdul Hassan Mohammed-Jawad

Food poisoning due to the bacteria is a big global problem in economically and human's health. This problem refers to an illness which is due to infection or the toxin exists in nature and the food that use. Milk is considered a nutritious food because it contains proteins and vitamins. The aim of this study is to detect and phylogeny characterization of staphylococcal enterotoxin B gene (Seb). A total of 200 milk and cheese samples were screened. One hundred ten isolates of Staphylococcus aureus pre-confirmed using selective and differential media with biochemical tests. Genomic DNA was extracted from the isolates and the SEB gene detects using conventional PCR with specific primers. Three staphylococcus aureus isolates were found to be positive for Seb gene using PCR and confirmed by sequencing. Sequence homology showed variety range of identity starting from (100% to 38%). Phylogenetic tree analyses show that samples (6 and 5) are correlated with S. epidermidis. This study discovered that isolates (A6-RLQ and A5-RLQ) are significantly clustered in a group with non- human pathogen Staphylococcus agnetis.


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