| Literature DB >> 36260188 |
Julalak Chuprom1,2,3, Kamchai Kidsin4, Suthinee Sangkanu2, Veeranoot Nissapatorn2, Christophe Wiart5, Maria de Lourdes Pereira6, Tuempong Wongtawan1,7, Mareena Daus8, Dennapa Saeloh Sotthibandhu9, Varomyalin Tipmanee10, Alok K Paul11, Charles Norman Scholfield1,7, Masyitah Binti Zulkipli12, Nor Hayati Abdullah13, Watcharapong Mitsuwan14,15,16.
Abstract
This study aimed to assess antibacterial activity of Knema retusa wood extract (KRe) against antibiotic resistant staphylococci which are causative agents of bovine mastitis. From 75 cases of intramammary infections in dairy cows, 66 staphylococcal isolates were collected, including 11 Staphylococcus aureus isolates (17%) and 55 coagulase-negative staphylococci (83%). Sixty isolates (91%) formed strong biofilms. KRe had minimal inhibitory concentrations (MIC) and minimal bactericidal concentrations (MBC) against the isolates ranging 32-256 ug/mL and 64-512 ug/mL, respectively. Two-hour KRe exposures at 4×MIC, viabilities of S. aureus and S. haemolyticus decreased by 3 log10 compared to the control. Scanning EM (SEM) showed that KRe disrupted the bacterial cells of both species. KRe at 1/16×MIC significantly inhibited biofilm formation (P < 0.05) in both S. aureus and S. haemolyticus. At 1/2×MIC, S. aureus and S. haemolyticus biofilm inhibition ranged from 75 to 99%. Cells within established biofilms were disrupted 66-83% by KRe at 32×MIC. Moreover, 1/2×MIC KRe reduced bacterial adhesion to glass surfaces observed by SEM. According to GC-MS analysis, the major compound in KRe was endo-2-hydroxy-9,9-(ethylenedioxy)-1-carbethoxy bicyclo [3.3.1] nonane (E2N). Molecular docking analysis of E2N has a high affinity for staphylococcal accessory regulator A (SarA), binding free-energy - 6.40kcal/mol. The results suggested that KRe may have medicinal benefits by inhibiting the growth, biofilm, and adhesion of antibiotic resistant staphylococci isolated from bovine mastitis.Entities:
Keywords: Biofilms; Bovine mastitis; Knema retusa extract; Staphylococci; Viability
Year: 2022 PMID: 36260188 DOI: 10.1007/s11259-022-09999-0
Source DB: PubMed Journal: Vet Res Commun ISSN: 0165-7380 Impact factor: 2.816