• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Sustained Coinfections with and in Cystic Fibrosis.囊性纤维化中 与 的持续共感染。
Am J Respir Crit Care Med. 2021 Feb 1;203(3):328-338. doi: 10.1164/rccm.202004-1322OC.
2
Staphylococcus aureus in the airways of cystic fibrosis patients - A retrospective long-term study.囊性纤维化患者气道中的金黄色葡萄球菌 - 一项回顾性长期研究。
Int J Med Microbiol. 2018 Aug;308(6):631-639. doi: 10.1016/j.ijmm.2018.02.003. Epub 2018 Feb 24.
3
Association of Diverse Staphylococcus aureus Populations with Pseudomonas aeruginosa Coinfection and Inflammation in Cystic Fibrosis Airway Infection.不同金黄色葡萄球菌种群与铜绿假单胞菌共感染和炎症在囊性纤维化气道感染中的关联。
mSphere. 2021 Jun 30;6(3):e0035821. doi: 10.1128/mSphere.00358-21. Epub 2021 Jun 23.
4
Multicenter Observational Study on Factors and Outcomes Associated with Various Methicillin-Resistant Staphylococcus aureus Types in Children with Cystic Fibrosis.囊性纤维化患儿中与各种耐甲氧西林金黄色葡萄球菌类型相关的因素及结局的多中心观察性研究
Ann Am Thorac Soc. 2015 Jun;12(6):864-71. doi: 10.1513/AnnalsATS.201412-596OC.
5
Genotypic and Phenotypic Diversity of Staphylococcus aureus Isolates from Cystic Fibrosis Patient Lung Infections and Their Interactions with Pseudomonas aeruginosa.囊性纤维化肺病患者肺部感染金黄色葡萄球菌分离株的基因表型多样性及其与铜绿假单胞菌的相互作用。
mBio. 2020 Jun 23;11(3):e00735-20. doi: 10.1128/mBio.00735-20.
6
Palivizumab prophylaxis in infants with cystic fibrosis does not delay first isolation of Pseudomonas aeruginosa or Staphylococcus aureus.对患有囊性纤维化的婴儿进行帕利珠单抗预防,并不会延迟首次分离出铜绿假单胞菌或金黄色葡萄球菌的时间。
Eur J Pediatr. 2017 Jul;176(7):891-897. doi: 10.1007/s00431-017-2926-8. Epub 2017 May 16.
7
Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients.长期、低剂量阿奇霉素治疗可降低丹麦囊性纤维化(CF)患者金黄色葡萄球菌的感染发生率,但会增加其对大环内酯类药物的耐药性。
J Cyst Fibros. 2009 Jan;8(1):58-62. doi: 10.1016/j.jcf.2008.09.001. Epub 2008 Oct 11.
8
Concordant genotype of upper and lower airways P aeruginosa and S aureus isolates in cystic fibrosis.囊性纤维化患者上、下呼吸道分离出的铜绿假单胞菌和金黄色葡萄球菌的基因型一致。
Thorax. 2009 Jun;64(6):535-40. doi: 10.1136/thx.2008.104711. Epub 2009 Mar 11.
9
Impact of colonizing organism in the respiratory tract on the incidence, duration, and time between subsequent hospitalizations among patients with cystic fibrosis.定植于呼吸道的微生物对囊性纤维化患者住院的发生率、持续时间和间隔时间的影响。
Am J Infect Control. 2019 Jul;47(7):750-754. doi: 10.1016/j.ajic.2018.12.021. Epub 2019 Feb 5.
10
Pseudomonas aeruginosa in cystic fibrosis patients with G551D-CFTR treated with ivacaftor.接受依伐卡托治疗的携带G551D-CFTR的囊性纤维化患者中的铜绿假单胞菌
Clin Infect Dis. 2015 Mar 1;60(5):703-12. doi: 10.1093/cid/ciu944. Epub 2014 Nov 25.

引用本文的文献

1
A comprehensive review of the pathogenic mechanisms of : synergistic effects of virulence factors, quorum sensing, and biofilm formation.毒力因子、群体感应和生物膜形成的协同作用致病机制的全面综述。
Front Microbiol. 2025 Jul 21;16:1619626. doi: 10.3389/fmicb.2025.1619626. eCollection 2025.
2
Modeling Pseudomonas aeruginosa-Staphylococcus aureus interactions in zebrafish to assess the host inflammatory response upon co-infection.在斑马鱼中模拟铜绿假单胞菌与金黄色葡萄球菌的相互作用,以评估共感染时宿主的炎症反应。
Sci Rep. 2025 Jul 4;15(1):23965. doi: 10.1038/s41598-025-08459-4.
3
Mastoparan-S from Sphodromantis viridis exhibits antimicrobial activity by disrupting bacterial membranes.来自绿巨螳螂的马斯托帕兰-S通过破坏细菌膜表现出抗菌活性。
AMB Express. 2025 Jul 3;15(1):99. doi: 10.1186/s13568-025-01908-3.
4
Unlocking Enhanced Efficacy of Aminoglycoside Antibiotics Against Pseudomonas aeruginosa.解锁氨基糖苷类抗生素对铜绿假单胞菌的增强疗效。
Microb Biotechnol. 2025 Jun;18(6):e70174. doi: 10.1111/1751-7915.70174.
5
Modeling reciprocal adaptation of and co-isolates in artificial sputum medium.在人工痰液培养基中模拟[具体内容1]和[具体内容2]共分离株的相互适应性。
Biofilm. 2025 Apr 11;9:100279. doi: 10.1016/j.bioflm.2025.100279. eCollection 2025 Jun.
6
Development and validation of a risk prediction model for 30-day readmission in elderly type 2 diabetes patients complicated with heart failure: a multicenter, retrospective study.老年2型糖尿病合并心力衰竭患者30天再入院风险预测模型的开发与验证:一项多中心回顾性研究
Front Endocrinol (Lausanne). 2025 Feb 27;16:1534516. doi: 10.3389/fendo.2025.1534516. eCollection 2025.
7
Mutations in the Staphylococcus aureus Global Regulator CodY confer tolerance to an interspecies redox-active antimicrobial.金黄色葡萄球菌全局调节因子CodY中的突变赋予了对种间氧化还原活性抗菌剂的耐受性。
PLoS Genet. 2025 Mar 7;21(3):e1011610. doi: 10.1371/journal.pgen.1011610. eCollection 2025 Mar.
8
Different aspects of Pseudomonas aeruginosa biofilm: an in-depth analysis from formation to detection.铜绿假单胞菌生物膜的不同方面:从形成到检测的深入分析
Naunyn Schmiedebergs Arch Pharmacol. 2025 Mar 5. doi: 10.1007/s00210-025-03971-w.
9
Dual RNA sequencing of a co-culture model of Pseudomonas aeruginosa and human 2D upper airway organoids.铜绿假单胞菌与人类二维上呼吸道类器官共培养模型的双重RNA测序
Sci Rep. 2025 Jan 17;15(1):2222. doi: 10.1038/s41598-024-82500-w.
10
Genetic Concordance of Staphylococcus aureus From Oropharyngeal and Sputum Cultures in People With Cystic Fibrosis.囊性纤维化患者口咽和痰液培养出的金黄色葡萄球菌的基因一致性
Pediatr Pulmonol. 2025 Jan;60(1):e27475. doi: 10.1002/ppul.27475.

本文引用的文献

1
Interspecies interactions induce exploratory motility in .种间相互作用诱导 . 的探索性运动。
Elife. 2019 Nov 12;8:e47365. doi: 10.7554/eLife.47365.
2
Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation.囊性纤维化和 G551D 突变患者用依伐卡托治疗后气道微生物组和炎症的变化。
Ann Am Thorac Soc. 2020 Feb;17(2):212-220. doi: 10.1513/AnnalsATS.201907-493OC.
3
Anaerobiosis influences virulence properties of Pseudomonas aeruginosa cystic fibrosis isolates and the interaction with Staphylococcus aureus.厌氧条件影响铜绿假单胞菌囊性纤维化分离株的毒力特性及其与金黄色葡萄球菌的相互作用。
Sci Rep. 2019 May 1;9(1):6748. doi: 10.1038/s41598-019-42952-x.
4
Direct Lung Sampling Indicates That Established Pathogens Dominate Early Infections in Children with Cystic Fibrosis.直接肺采样表明,在患有囊性纤维化的儿童中,既定病原体在早期感染中占主导地位。
Cell Rep. 2019 Apr 23;27(4):1190-1204.e3. doi: 10.1016/j.celrep.2019.03.086.
5
Pathogen acquisition in patients with cystic fibrosis receiving ivacaftor or lumacaftor/ivacaftor.接受 ivacaftor 或 lumacaftor/ivacaftor 治疗的囊性纤维化患者的病原体获得情况。
Pediatr Pulmonol. 2019 Aug;54(8):1200-1208. doi: 10.1002/ppul.24341. Epub 2019 Apr 22.
6
Respiratory Bacterial Culture Sampling in Expectorating and Non-expectorating Patients With Cystic Fibrosis.囊性纤维化咳痰和不咳痰患者的呼吸道细菌培养采样
Front Pediatr. 2018 Dec 18;6:403. doi: 10.3389/fped.2018.00403. eCollection 2018.
7
Eradication of persistent methicillin-resistant Staphylococcus aureus infection in cystic fibrosis.消除囊性纤维化患者耐甲氧西林金黄色葡萄球菌的持续感染。
J Cyst Fibros. 2019 May;18(3):357-363. doi: 10.1016/j.jcf.2018.07.005. Epub 2018 Aug 18.
8
The CF-Sputum Induction Trial (CF-SpIT) to assess lower airway bacterial sampling in young children with cystic fibrosis: a prospective internally controlled interventional trial.囊性纤维化患儿下呼吸道细菌采样评估的 CF-诱导痰试验(CF-SpIT):一项前瞻性内部对照干预性试验。
Lancet Respir Med. 2018 Jun;6(6):461-471. doi: 10.1016/S2213-2600(18)30171-1. Epub 2018 May 16.
9
Staphylococcus aureus in the airways of cystic fibrosis patients - A retrospective long-term study.囊性纤维化患者气道中的金黄色葡萄球菌 - 一项回顾性长期研究。
Int J Med Microbiol. 2018 Aug;308(6):631-639. doi: 10.1016/j.ijmm.2018.02.003. Epub 2018 Feb 24.
10
The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis.金黄色葡萄球菌与囊性纤维化患儿支气管扩张症的相关性。
J Cyst Fibros. 2018 Jul;17(4):462-469. doi: 10.1016/j.jcf.2017.12.002. Epub 2017 Dec 21.

囊性纤维化中 与 的持续共感染。

Sustained Coinfections with and in Cystic Fibrosis.

机构信息

Stead Family Department of Pediatrics.

Department of Internal Medicine, and.

出版信息

Am J Respir Crit Care Med. 2021 Feb 1;203(3):328-338. doi: 10.1164/rccm.202004-1322OC.

DOI:10.1164/rccm.202004-1322OC
PMID:32750253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7874317/
Abstract

: and often infect the airways in cystic fibrosis (CF). Because registry studies show higher prevalence of versus in older patients with CF, a common assumption is that replaces over time. , can outgrow and kill . However, it is unknown how rapidly replaces in patients with CF.: We studied a longitudinal cohort of children and adults with CF who had quantitative sputum cultures. We determined the abundance of and in cfu/ml. We determined the duration and persistence of infections and measured longitudinal changes in culture positivity and abundance for each organism.: Between 2004 and 2017, 134 patients had ≥10 quantitative cultures, with median observation time of 10.15 years. One hundred twenty-four patients had at least one positive culture for , and 123 had at least one positive culture for . Both species had median abundance of >10 cfu/ml. Culture abundance was stable over time for both organisms. There was an increase in the prevalence of / coinfection but no decrease in prevalence within individuals over time.: and are abundant in CF sputum cultures. Contrary to common assumption, we found no pattern of replacement of by . Many patients with CF have durable long-term coinfection with these organisms. New strategies are needed to prevent and treat these infections.

摘要

和 经常感染囊性纤维化(CF)患者的气道。由于登记研究表明,随着 CF 患者年龄的增长, 的患病率高于 ,因此人们普遍认为 会随着时间的推移取代 。然而,目前尚不清楚 在 CF 患者中取代 的速度有多快。我们研究了一组患有 CF 的儿童和成人的纵向队列,这些患者进行了定量痰液培养。我们确定了 cfu/ml 中 和 的丰度。我们确定了感染的持续时间和持续性,并测量了每种生物体的培养阳性和丰度的纵向变化。在 2004 年至 2017 年间,134 名患者进行了≥10 次定量培养,中位观察时间为 10.15 年。124 名患者至少有一次 的阳性培养,123 名患者至少有一次 的阳性培养。两种生物的丰度中位数均>10 cfu/ml。两种生物体的培养物丰度随时间保持稳定。/混合感染的患病率增加,但个体中 的患病率随时间没有下降。和 在 CF 痰液培养物中含量丰富。与普遍的假设相反,我们没有发现 被 取代的模式。许多 CF 患者长期存在这两种生物体的混合感染。需要新的策略来预防和治疗这些感染。