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牙刷可能会将细菌传播至囊性纤维化患者的下呼吸道。

Toothbrushes may convey bacteria to the cystic fibrosis lower airways.

作者信息

Passarelli Mantovani Rebeca, Sandri Angela, Boaretti Marzia, Grilli Alessandra, Volpi Sonia, Melotti Paola, Burlacchini Gloria, Lleò Maria M, Signoretto Caterina

机构信息

Department of Diagnostics and Public Health, Microbiology Section, University of Verona, Verona, Italy.

Cystic Fibrosis Center, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.

出版信息

J Oral Microbiol. 2019 Aug 7;11(1):1647036. doi: 10.1080/20002297.2019.1647036. eCollection 2019.

DOI:10.1080/20002297.2019.1647036
PMID:31489126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6713191/
Abstract

Recent findings indicate that the oral cavity acts as a bacterial reservoir and might contribute to the transmission of bacteria to the lower airways. Control of a potentially pathogenic microbiota might contribute to prevent the establishment of chronic infection in cystic fibrosis. We evaluated the presence of CF microorganisms in saliva and toothbrushes of CF patients and verify their possible transmission to lower airways. : We assessed the presence of , and yeasts in saliva, toothbrushes and sputum of 38 CF patients and assessed the clonal identity of the strains occurring contemporary in multiple sites by PFGE. : At least one of the investigated species was isolated from 60 saliva samples and 23 toothbrushes. was the most abundant species, followed by Candida spp. 31 patients contemporary had the same species in sputum and saliva/toothbrush: in most cases, clonal identity of the strains among the different sites was confirmed. : Toothbrushes may be sources of oral contamination and might act as reservoirs favoring transmission of potentially pathogenic microorganisms from the environment to the oral cavity and eventually to the LAW. Oral hygiene and toothbrush care are important strategies to prevent CF lung infections.

摘要

近期研究结果表明,口腔充当着细菌储存库的角色,可能会促使细菌传播至下呼吸道。控制潜在致病性微生物群可能有助于预防囊性纤维化患者慢性感染的发生。我们评估了囊性纤维化(CF)患者唾液和牙刷中CF微生物的存在情况,并验证它们向下呼吸道传播的可能性。我们评估了38例CF患者唾液、牙刷和痰液中细菌、酵母菌的存在情况,并通过脉冲场凝胶电泳(PFGE)评估多个部位同时出现的菌株的克隆一致性。在60份唾液样本和23把牙刷中至少分离出一种被调查的菌种。金黄色葡萄球菌是最常见的菌种,其次是念珠菌属。31例患者的痰液与唾液/牙刷中同时存在相同菌种:在大多数情况下,不同部位菌株的克隆一致性得到了证实。牙刷可能是口腔污染的来源,可能充当有利于潜在致病微生物从环境传播至口腔并最终传播至下呼吸道的储存库。口腔卫生和牙刷护理是预防CF肺部感染的重要策略。

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本文引用的文献

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Elimination of Australian epidemic strain (AES1) pseudomonas aeruginosa in a pediatric cystic fibrosis center.消除儿科囊性纤维化中心的澳大利亚流行株(AES1)铜绿假单胞菌。
Pediatr Pulmonol. 2018 Nov;53(11):1498-1503. doi: 10.1002/ppul.24173. Epub 2018 Oct 12.
2
Epidemiology of CF: How registries can be used to advance our understanding of the CF population.CF 的流行病学:登记系统如何帮助我们深入了解 CF 群体。
J Cyst Fibros. 2018 May;17(3):297-305. doi: 10.1016/j.jcf.2017.11.013. Epub 2017 Dec 21.
3
Sinus bacteriology in patients with cystic fibrosis or primary ciliary dyskinesia: A systematic review.
臭氧超细微气泡水对口腔和上呼吸道中的致病菌具有杀菌活性,并对污染的医疗保健设备进行消毒。
PLoS One. 2023 Apr 12;18(4):e0284115. doi: 10.1371/journal.pone.0284115. eCollection 2023.
4
Biofilm on Toothbrushes of Children with Cystic Fibrosis: A Potential Source of Lung Re-Infection after Antibiotic Treatment?囊性纤维化患儿牙刷上的生物膜:抗生素治疗后肺部再次感染的潜在来源?
Materials (Basel). 2022 Mar 14;15(6):2139. doi: 10.3390/ma15062139.
5
Role of Salivary Biomarkers in Cystic Fibrosis: A Systematic Review.唾液生物标志物在囊性纤维化中的作用:系统评价。
Biomed Res Int. 2022 Jan 19;2022:5818840. doi: 10.1155/2022/5818840. eCollection 2022.
囊性纤维化或原发性纤毛运动障碍患者的鼻窦细菌学:一项系统评价。
Am J Rhinol Allergy. 2017 Sep 1;31(5):293-298. doi: 10.2500/ajra.2017.31.4461.
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Evidence summary: the relationship between oral health and pulmonary disease.证据总结:口腔健康与肺部疾病之间的关系
Br Dent J. 2017 Apr 7;222(7):527-533. doi: 10.1038/sj.bdj.2017.315.
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Arch Pediatr. 2015 Dec;22(12):1240-6. doi: 10.1016/j.arcped.2015.09.023. Epub 2015 Nov 17.
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Eur Arch Paediatr Dent. 2014 Aug;15(4):275-80. doi: 10.1007/s40368-014-0112-5. Epub 2014 Feb 26.