Therapeutic Effects of Inhibitor of ompA Expression against Carbapenem-Resistant Acinetobacter baumannii Strains

被引:11
作者
Na, Seok-Hyeon [1 ]
Jeon, Hyejin [2 ]
Oh, Man-Hwan [3 ]
Kim, Yoo-Jeong [2 ]
Chu, Mingi [4 ]
Lee, Ill-Young [4 ]
Lee, Je-Chul [2 ]
机构
[1] Korea Dis Control & Prevent, Natl Inst Hlth, Natl Inst Infect Dis, Ctr Infect Dis Res,Div Antimicrobial Resistance R, Cheongju 28159, South Korea
[2] Kyungpook Natl Univ, Sch Med, Dept Microbiol, Daegu 41944, South Korea
[3] Dankook Univ, Dept Microbiol, Coll Sci & Technol, Cheonan 16890, South Korea
[4] Korea Res Inst Chem Technol, Bio & Drug Discovery Div, Res Ctr Ecofriendly New Mat, Daejeon 34114, South Korea
关键词
Acinetobacter baumannii; ompA promoter inhibitor; compound; 62520; anti-virulence; bacteriostatic agent; MEMBRANE PROTEIN-A; MULTIDRUG-RESISTANT; ANTIMICROBIAL RESISTANCE;
D O I
10.3390/ijms222212257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The widespread of carbapenem-resistant Acinetobacter baumannii (CRAB) is of great concern in clinical settings worldwide. It is urgent to develop new therapeutic agents against this pathogen. This study aimed to evaluate the therapeutic potentials of compound 62520, which has been previously identified as an inhibitor of the ompA promoter activity of A. baumannii, against CRAB isolates, both in vitro and in vivo. Compound 62520 was found to inhibit the ompA expression and biofilm formation in A. baumannii ATCC 17978 at sub-inhibitory concentrations in a dose-dependent manner. These inhibitory properties were also observed in clinical CRAB isolates belonging to sequence type (ST) 191. Additionally, compound 62520 exhibited a bacteriostatic activity against clinical clonal complex (CC) 208 CRAB isolates, including ST191, and ESKAPE pathogens. This bacteriostatic activity was not different between STs of CRAB isolates. Bacterial clearance was observed in mice infected with bioimaging A. baumannii strain 24 h after treatment with compound 62520. Compound 62520 was shown to significantly increase the survival rates of both immunocompetent and neutropenic mice infected with A. baumannii ATCC 17978. This compound also increased the survival rates of mice infected with clinical CRAB isolate. These results suggest that compound 62520 is a promising scaffold to develop a novel therapeutic agent against CRAB infections.
引用
收藏
页数:13
相关论文
共 38 条
[1]   AOA-2 Derivatives as Outer Membrane Protein A Inhibitors for Treatment of Gram-Negative Bacilli Infections [J].
Ayerbe-Algaba, Rafael ;
Bayo, Nuria ;
Verdu, Ester ;
Parra-Millan, Raquel ;
Seco, Jesus ;
Teixido, Meritxell ;
Pachon, Jeronimo ;
Giralt, Ernest ;
Smani, Younes .
FRONTIERS IN MICROBIOLOGY, 2021, 12
[2]  
Ayobami Olaniyi, 2019, Emerg Microbes Infect, V8, P1747, DOI 10.1080/22221751.2019.1698273
[3]   The biology and future prospects of antivirulence therapies [J].
Cegelski, Lynette ;
Marshall, Garland R. ;
Eldridge, Gary R. ;
Hultgren, Scott J. .
NATURE REVIEWS MICROBIOLOGY, 2008, 6 (01) :17-27
[4]   Virstatin inhibits biofilm formation and motility of Acinetobacter baumannii [J].
Chabane, Yassine Nait ;
Ben Mlouka, Mohamed ;
Alexandre, Stephane ;
Nicol, Marion ;
Marti, Sara ;
Pestel-Caron, Martine ;
Vila, Jordi ;
Jouenne, Thierry ;
De, Emmanuelle .
BMC MICROBIOLOGY, 2014, 14
[5]   Outer membrane protein 38 of Acinetobacter baumannii localizes to the mitochondria and induces apoptosis of epithelial cells [J].
Choi, CH ;
Lee, EY ;
Lee, YC ;
Park, TI ;
Kim, HJ ;
Hyun, SH ;
Kim, SA ;
Lee, SK ;
Lee, JC .
CELLULAR MICROBIOLOGY, 2005, 7 (08) :1127-1138
[6]   Acinetobacter baumannii outer membrane protein A targets the nucleus and induces cytotoxicity [J].
Choi, Chul Hee ;
Hyun, Sung Hee ;
Lee, Ji Young ;
Lee, Jun Sik ;
Lee, Yong Seok ;
Kim, Soon Ae ;
Chae, Jeong-Pil ;
Yoo, Seung Min ;
Lee, Je Chul .
CELLULAR MICROBIOLOGY, 2008, 10 (02) :309-319
[7]   Acinetobacter baumannii invades epithelial cells and outer membrane protein A mediates interactions with epithelial cells [J].
Choi, Chul Hee ;
Lee, Jun Sik ;
Lee, Yoo Chul ;
Park, Tae In ;
Lee, Je Chul .
BMC MICROBIOLOGY, 2008, 8 (1)
[8]   An increasing threat in hospitals:: multidrug-resistant Acinetobacter baumannii [J].
Dijkshoorn, Lenie ;
Nemec, Alexandr ;
Seifert, Harald .
NATURE REVIEWS MICROBIOLOGY, 2007, 5 (12) :939-951
[9]   Acinetobacter baumannii OmpA Is a Selective Antibiotic Permeant Porin [J].
Iyer, Ramkumar ;
Moussa, Samir H. ;
Durand-Reville, Thomas F. ;
Tommasi, Ruben ;
Miller, Alita .
ACS INFECTIOUS DISEASES, 2018, 4 (03) :373-381
[10]   Acinetobacter baumannii Outer Membrane Vesicles Elicit a Potent Innate Immune Response via Membrane Proteins [J].
Jun, So Hyun ;
Lee, Jung Hwa ;
Kim, Bo Ra ;
Kim, Seung Il ;
Park, Tae In ;
Lee, Je Chul ;
Lee, Yoo Chul .
PLOS ONE, 2013, 8 (08)