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用于对抗肺炎支原体感染和疾病的窄谱药物的潜在分子靶点

Potential Molecular Targets for Narrow-Spectrum Agents to Combat Mycoplasma pneumoniae Infection and Disease.

作者信息

Balish Mitchell F, Distelhorst Steven L

机构信息

Department of Microbiology, Miami University Oxford, OH, USA.

出版信息

Front Microbiol. 2016 Feb 25;7:205. doi: 10.3389/fmicb.2016.00205. eCollection 2016.

Abstract

As Mycoplasma pneumoniae macrolide resistance grows and spreads worldwide, it is becoming more important to develop new drugs to prevent infection or limit disease. Because other mycoplasma species have acquired resistance to other classes of antibiotics, it is reasonable to presume that M. pneumoniae can do the same, so switching to commonly used antibiotics like fluoroquinolones will not result in forms of therapy with long-term utility. Moreover, broad-spectrum antibiotics can have serious consequences for the patient, as these drugs may have severe impacts on the natural microbiota of the individual, compromising the health of the patient either short-term or long-term. Therefore, developing narrow-spectrum antibiotics that effectively target only M. pneumoniae and no more than a small portion of the microbiota is likely to yield impactful, positive results that can be used perhaps indefinitely to combat M. pneumoniae. Development of these agents requires a deep understanding of the basic biology of M. pneumoniae, in many areas deeper than what is currently known. In this review, we discuss potential targets for new, narrow-spectrum agents and both the positive and negative aspects of selecting these targets, which include toxic molecules, metabolic pathways, and attachment and motility. By gathering this information together, we anticipate that it will be easier for researchers to evaluate topics of priority for study of M. pneumoniae.

摘要

随着肺炎支原体对大环内酯类药物的耐药性在全球范围内不断增加和传播,开发新药以预防感染或控制疾病变得越发重要。由于其他支原体物种已对其他类别的抗生素产生耐药性,因此可以合理推测肺炎支原体也能如此,所以转而使用氟喹诺酮等常用抗生素不会产生具有长期效用的治疗方式。此外,广谱抗生素可能会给患者带来严重后果,因为这些药物可能会对个体的自然微生物群产生严重影响,无论在短期还是长期都会损害患者的健康。因此,开发仅有效靶向肺炎支原体且不影响超过一小部分微生物群的窄谱抗生素,可能会产生有影响力的积极成果,或许可以无限期地用于对抗肺炎支原体。开发这些药物需要深入了解肺炎支原体的基础生物学,在许多方面要比目前所知的更深入。在这篇综述中,我们讨论了新型窄谱药物的潜在靶点以及选择这些靶点的利弊,这些靶点包括毒性分子、代谢途径以及附着和运动。通过收集这些信息,我们预计研究人员将更容易评估肺炎支原体研究的优先课题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3da/4766277/26850a31aa55/fmicb-07-00205-g001.jpg

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