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甲硝唑、环丙沙星和亚胺培南低于最低抑菌浓度值对……生长和毒素产生的影响

Effect of sub-MIC values of metronidazole, ciprofloxacin, and imipenem on the growth and toxin production in .

作者信息

Shayegan Mehr Farahnaz Sadat, Azimirad Masoumeh, Mansouri Gilani Seyedeh Nazanin, Ghafurian Ayub, Yadegar Abbas

机构信息

Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Gastroenterol Hepatol Bed Bench. 2019;12(Suppl1):S163-S168.

PMID:32099618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7011067/
Abstract

AIM

This study intends to investigate the effect of sub-minimum inhibitory concentration (sub-MIC) of metronidazole, ciprofloxacin, and imipenem on the growth and toxin production in .

BACKGROUND

is the most common causative agent of hospital-acquired diarrhea. Toxin production in appears to be a critical process for induction of the disease. Several factors such as antibiotics can facilitate growth and toxin production in .

METHODS

Five strains were grown with and without sub-MIC concentrations of metronidazole, ciprofloxacin, and imipenem (0.5x MIC). The bacterial growth was measured by density at OD620 nm in 0, 4, 8, 12 and 24 h post inoculation. Toxin production was detected using ELISA in culture supernatants as well as in cell pellet.

RESULTS

The five strains showed minor growth variations in the presence and absence of antibiotic sub-MIC values, except for metronidazole, in which the sub-MIC concentration reduced the growth rate of the resistant isolate in comparison with the control without antibiotic. There were no significant variations in the levels of toxin production with the sub-MIC values of antibiotics examined in comparison with antibiotic-free controls. However, the amount of toxin production in the culture supernatant was greater than in the cell pellet.

CONCLUSION

The findings of this study suggested that sub-MIC concentrations of antibiotics may have minor effects on bacterial growth and toxin production of . Taken together, these findings suggest that presence of antimicrobial agents increased expression levels of certain genes, particularly virulence genes, which may help to survive.

摘要

目的

本研究旨在调查甲硝唑、环丙沙星和亚胺培南的亚最小抑菌浓度(亚 MIC)对[研究对象]生长和毒素产生的影响。

背景

[研究对象]是医院获得性腹泻最常见的病原体。[研究对象]产生毒素似乎是诱发该疾病的关键过程。抗生素等多种因素可促进[研究对象]的生长和毒素产生。

方法

五株[研究对象]菌株分别在有和没有亚 MIC 浓度的甲硝唑、环丙沙星和亚胺培南(0.5x MIC)的情况下培养。在接种后 0、4、8、12 和 24 小时通过 OD620 nm 处的密度测量细菌生长。使用 ELISA 在培养上清液以及细胞沉淀中检测毒素产生。

结果

除甲硝唑外,五株菌株在有无抗生素亚 MIC 值的情况下生长变化较小,与无抗生素对照相比,甲硝唑的亚 MIC 浓度降低了耐药菌株的生长速率。与无抗生素对照相比,所检测抗生素的亚 MIC 值对毒素产生水平没有显著差异。然而,培养上清液中的毒素产生量大于细胞沉淀中的毒素产生量。

结论

本研究结果表明,抗生素的亚 MIC 浓度可能对[研究对象]的细菌生长和毒素产生有轻微影响。综上所述,这些发现表明抗菌剂的存在增加了某些基因,特别是毒力基因的表达水平,这可能有助于[研究对象]存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/7011067/c97daff84311/GHFBB-12-S163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/7011067/942f9ea50762/GHFBB-12-S163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/7011067/c97daff84311/GHFBB-12-S163-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/7011067/942f9ea50762/GHFBB-12-S163-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/7011067/c97daff84311/GHFBB-12-S163-g002.jpg

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本文引用的文献

1
Prevalence of binary-toxin genes ( and ) among clinical strains of isolated from diarrheal patients in Iran.从伊朗腹泻患者中分离出的 临床菌株中二元毒素基因( 和 )的流行情况。
Gastroenterol Hepatol Bed Bench. 2018 Winter;11(Suppl 1):59-65.
2
- From Colonization to Infection.- 从定植到感染。
Front Microbiol. 2018 Apr 10;9:646. doi: 10.3389/fmicb.2018.00646. eCollection 2018.
3
Clinical Practice Guidelines for Clostridium difficile Infection in Adults and Children: 2017 Update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA).
临床实践指南:成人和儿童艰难梭菌感染:美国传染病学会(IDSA)和美国医疗保健流行病学学会(SHEA) 2017 年更新。
Clin Infect Dis. 2018 Mar 19;66(7):e1-e48. doi: 10.1093/cid/cix1085.
4
Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease.肠道微生物群:在病原体定植、免疫反应和炎症性疾病中的作用。
Immunol Rev. 2017 Sep;279(1):70-89. doi: 10.1111/imr.12567.
5
Risk factors for infections - an overview of the evidence base and challenges in data synthesis.感染的危险因素——证据基础概述及数据综合的挑战。
J Glob Health. 2017 Jun;7(1):010417. doi: 10.7189/jogh.07.010417.
6
Control of Clostridium difficile Physiopathology in Response to Cysteine Availability.响应半胱氨酸可用性对艰难梭菌病理生理学的控制
Infect Immun. 2016 Jul 21;84(8):2389-405. doi: 10.1128/IAI.00121-16. Print 2016 Aug.
7
Clostridium difficile infection.艰难梭菌感染。
Nat Rev Dis Primers. 2016 Apr 7;2:16020. doi: 10.1038/nrdp.2016.20.
8
Pseudomembranous colitis.伪膜性结肠炎
Dis Mon. 2015 May;61(5):181-206. doi: 10.1016/j.disamonth.2015.01.006. Epub 2015 Mar 11.
9
Treatment failure and recurrence of Clostridium difficile infection following treatment with vancomycin or metronidazole: a systematic review of the evidence.万古霉素或甲硝唑治疗后艰难梭菌感染的治疗失败和复发:证据的系统评价。
Int J Antimicrob Agents. 2012 Jul;40(1):1-8. doi: 10.1016/j.ijantimicag.2012.01.004. Epub 2012 Mar 6.
10
Clostridium difficile: a problem of concern in developed countries and still a mystery in Latin America.艰难梭菌:发达国家关注的问题,在拉丁美洲仍未解之谜。
J Med Microbiol. 2012 Feb;61(Pt 2):169-179. doi: 10.1099/jmm.0.037077-0. Epub 2011 Nov 24.