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β-内酰胺/β-内酰胺酶抑制剂组合对多重耐药鼠伤寒沙门氏菌的抗生物膜活性

Antibiofilm Activity of β-Lactam/β-Lactamase Inhibitor Combination against Multidrug-Resistant Typhimurium.

作者信息

Laure Nana Nguefang, Ahn Juhee

机构信息

Department of Biomedical Science, Kangwon National University, Chuncheon 24341, Korea.

Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 24341, Korea.

出版信息

Pathogens. 2022 Mar 13;11(3):349. doi: 10.3390/pathogens11030349.

DOI:10.3390/pathogens11030349
PMID:35335673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8950422/
Abstract

This study was designed to assess the effect of β-lactam/β-lactamase inhibitor combinations on the inhibition of biofilm formation of Typhimurium. The anti-planktonic and anti-biofilm activities of ampicillin (AMP), ceftriaxone (CEF), and combination treatments of antibiotics and sulbactam (AMP + SUL and CEF + SUL) were evaluated against antibiotic-sensitive . Typhimurium ATCC 19585 (ST) and clinically isolated multidrug-resistant (MDR) . Typhimurium CCARM 8009 (ST). Compared to the control, the minimum inhibitory concentrations (MICs) of AMP against ST and CEF against ST were decreased from 32 to 16 μg/mL and 0.25 to 0.125 μg/mL, respectively, in the presence of SUL. The numbers of ST treated with AMP + SUL and CEF + SUL were effectively reduced by more than 2 logs after 4 h of incubation at 37 °C. The β-lactamase activities of ST and ST treated with AMP and CEF were reduced from 3.3 to 2.6 μmol/min/mL and from 8.3 to 3.4 μmol/min/mL, respectively, in the presence of SUL. The biofilm cell numbers of ST and ST were reduced at all treatments after 24 h of incubation at 37 °C. The biofilm cell numbers of ST and ST were reduced by more than 2 logs in the presence of SUL compared to the AMP and CEF alone. The lowest relative fitness level was 0.6 in ST treated with AMP + SUL, while no significant differences in the relative fitness were observed in ST. This study suggests that β-lactamase inhibitors (BLIs) could be used for controlling biofilm formation of β-lactamase-producing multidrug-resistant . Typhimurium.

摘要

本研究旨在评估β-内酰胺/β-内酰胺酶抑制剂组合对鼠伤寒沙门氏菌生物膜形成的抑制作用。针对抗生素敏感的鼠伤寒沙门氏菌ATCC 19585(ST)和临床分离的多重耐药(MDR)鼠伤寒沙门氏菌CCARM 8009(ST),评估了氨苄西林(AMP)、头孢曲松(CEF)以及抗生素与舒巴坦联合治疗(AMP + SUL和CEF + SUL)的抗浮游菌和抗生物膜活性。与对照组相比,在舒巴坦存在的情况下,AMP对ST的最低抑菌浓度(MIC)从32 μg/mL降至16 μg/mL,CEF对ST的MIC从0.25 μg/mL降至0.125 μg/mL。在37℃孵育4小时后,用AMP + SUL和CEF + SUL处理的ST菌数有效减少了2个对数以上。在舒巴坦存在的情况下,ST以及用AMP和CEF处理的ST的β-内酰胺酶活性分别从3.3 μmol/分钟/毫升降至2.6 μmol/分钟/毫升,从8.3 μmol/分钟/毫升降至3.4 μmol/分钟/毫升。在37℃孵育24小时后,所有处理组的ST生物膜细胞数均减少。与单独使用AMP和CEF相比,在舒巴坦存在的情况下,ST的生物膜细胞数减少了2个对数以上。用AMP + SUL处理的ST的最低相对适合度水平为0.6,而ST的相对适合度未观察到显著差异。本研究表明,β-内酰胺酶抑制剂(BLIs)可用于控制产β-内酰胺酶的多重耐药鼠伤寒沙门氏菌的生物膜形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/1617a2385eee/pathogens-11-00349-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/5988bf2a884f/pathogens-11-00349-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/b20dc2f1a86a/pathogens-11-00349-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/f5b4914ee1ed/pathogens-11-00349-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/f19ecd70bb82/pathogens-11-00349-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/1617a2385eee/pathogens-11-00349-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/5988bf2a884f/pathogens-11-00349-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/b20dc2f1a86a/pathogens-11-00349-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/f5b4914ee1ed/pathogens-11-00349-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/f19ecd70bb82/pathogens-11-00349-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ce/8950422/1617a2385eee/pathogens-11-00349-g005.jpg

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