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硫酸奎宁与细菌入侵。

Quinine sulfate and bacterial invasion.

作者信息

Wolf Ronni, Baroni Adone, Greco Rita, Donnarumma Giovanna, Ruocco Eleonora, Tufano Maria Antonietta, Ruocco Vincenzo

机构信息

Dermatology Unit, Kaplan Medical Center, Rechovot, Israel.

出版信息

Ann Clin Microbiol Antimicrob. 2002 Oct 22;1:5. doi: 10.1186/1476-0711-1-5.

Abstract

BACKGROUND

As many patients who receive antimalarial drugs for treatment of noninfectious, inflammatory diseases are also immunosuppressed and might have a concomitant bacterial infection, we studied the effectiveness of these drugs against bacterial infections, to find out whether they could protect against (and even treat) such conditions and obviate the need for an additional antibiotic drug.

METHODS

Effect of QS on bacterial growth: Escherichia coli (E. coli) HB101 pRI203 were cultured overnight at 37 degrees C in TSB and inoculated (approx 1 x 10(7) cells/ml) in MEM in the presence of QS at various concentrations (0, 50 and 100 microM).The effect of QS at concentration of 50 and 100 microM on the entry process of E. coli HB101 pRI203 into HeLa cells was studied under different experimental conditions: 1. QS was incubated with 3 x 10(5) HeLa cells for 60 min at 37 degrees C prior to infection. 2. QS was added to HeLa cell monolayers during the infection period.

RESULTS

QS showed no antibacterial activity after 24 h of incubation. The invasive efficiency of the bacteria was significantly inhibited at a dose-dependent manner, when QS was added to HeLa cells for 60 min at 37 degrees C prior to infection (condition 1), and to a lesser extent when added during the period of infection (condition 2).

CONCLUSIONS

Although the antimalarials are generally regarded as being inactive against most extracellular bacterial species, our results indicate that QS significantly inhibited the internalization/invasion efficacy of E. coli in the host cells.

摘要

背景

由于许多接受抗疟药物治疗非感染性炎症疾病的患者也存在免疫抑制,且可能伴有细菌感染,我们研究了这些药物对细菌感染的有效性,以确定它们是否能预防(甚至治疗)此类病症,从而无需额外使用抗生素。

方法

QS对细菌生长的影响:将大肠杆菌(E. coli)HB101 pRI203在37℃下于TSB中过夜培养,然后在含有不同浓度(0、50和100微摩尔)QS的MEM中接种(约1×10⁷个细胞/毫升)。在不同实验条件下研究了50和100微摩尔浓度的QS对大肠杆菌HB101 pRI203进入HeLa细胞的侵入过程的影响:1. 在感染前,将QS与3×10⁵个HeLa细胞在37℃下孵育60分钟。2. 在感染期间将QS添加到HeLa细胞单层中。

结果

孵育24小时后,QS未显示出抗菌活性。当在感染前(条件1)将QS添加到HeLa细胞中于37℃孵育60分钟时,细菌的侵入效率以剂量依赖性方式显著受到抑制,而在感染期间添加(条件2)时抑制程度较小。

结论

尽管抗疟药通常被认为对大多数细胞外细菌种类无活性,但我们的结果表明,QS显著抑制了大肠杆菌在宿主细胞中的内化/侵入效率。

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