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Metagenomic shotgun sequencing of blood to identify bacteria and viruses in leukemic febrile neutropenia.对血液进行宏基因组高通量测序以鉴定白血病发热性中性粒细胞减少症中的细菌和病毒。
PLoS One. 2022 Jun 16;17(6):e0269405. doi: 10.1371/journal.pone.0269405. eCollection 2022.
2
Standard rectal swabs as a surrogate sample for gut microbiome monitoring in intensive care.直肠拭子作为重症监护中肠道微生物组监测的替代样本。
BMC Microbiol. 2022 Apr 12;22(1):99. doi: 10.1186/s12866-022-02487-0.
3
On the robustness of inference of association with the gut microbiota in stool, rectal swab and mucosal tissue samples.在粪便、直肠拭子和黏膜组织样本中,与肠道微生物组关联的推断稳健性。
Sci Rep. 2021 Jul 21;11(1):14828. doi: 10.1038/s41598-021-94205-5.
4
Evaluation of the "AMR Direct Flow Chip Kit" DNA microarray for detecting antimicrobial resistance genes directly from rectal and nasopharyngeal clinical samples upon ICU admission.评估“AMR 直接流片试剂盒”DNA 微阵列,用于直接从 ICU 入院时的直肠和鼻咽临床样本中检测抗菌药物耐药基因。
Enferm Infecc Microbiol Clin (Engl Ed). 2021 Jun-Jul;39(6):276-278. doi: 10.1016/j.eimce.2020.05.014.
5
Metagenomic Sequencing as a Pathogen-Agnostic Clinical Diagnostic Tool for Infectious Diseases: a Systematic Review and Meta-analysis of Diagnostic Test Accuracy Studies.宏基因组测序作为一种病原体不可知的临床诊断工具在传染病中的应用:诊断测试准确性研究的系统评价和荟萃分析。
J Clin Microbiol. 2021 Aug 18;59(9):e0291620. doi: 10.1128/JCM.02916-20.
6
Management of fever and neutropenia in the adult patient with acute myeloid leukemia.成人急性髓系白血病患者发热与中性粒细胞减少的处理。
Expert Rev Anti Infect Ther. 2021 Mar;19(3):359-378. doi: 10.1080/14787210.2020.1820863. Epub 2020 Oct 5.
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Duration of Carbapenemase-Producing Enterobacteriaceae Carriage in Hospital Patients.产碳青霉烯酶肠杆菌科在医院患者中的携带时间。
Emerg Infect Dis. 2020 Sep;26(9):2182-2185. doi: 10.3201/eid2609.190592.
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Treatment of Relapsed Acute Myeloid Leukemia.复发急性髓系白血病的治疗。
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Epidemic of carbapenem-resistant Klebsiella pneumoniae in Europe is driven by nosocomial spread.欧洲耐碳青霉烯类肺炎克雷伯菌的流行是由医院内传播驱动的。
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评估鸟枪法宏基因组学方法在检测急性白血病康复的培养阴性患者中产生超广谱β-内酰胺酶和/或碳青霉烯酶细菌方面的应用

Evaluation of a Shotgun Metagenomics Approach for Detection of ESBL- and/or Carbapenemase-Producing in Culture Negative Patients Recovered from Acute Leukemia.

作者信息

Lumbreras-Iglesias Pilar, Sabater Carlos, Fernández Moreno Ainhoa, López de Ugarriza Paula, Fernández-Verdugo Ana, Margolles Abelardo, Rodicio María Rosario, Bernal Teresa, Fernández Javier

机构信息

Traslational Microbiology Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain.

Department of Clinical Microbiology, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Spain.

出版信息

Microorganisms. 2023 Feb 4;11(2):402. doi: 10.3390/microorganisms11020402.

DOI:10.3390/microorganisms11020402
PMID:36838367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9964539/
Abstract

Patients diagnosed with acute leukemia (AL) have a weakened immune system. Infections acquired by these patients are cause for concern and especially worrisome when Gram-negative multidrug-resistant (MDR) bacteria are involved, as they are difficult to treat, especially in the case of ESBL- and/or carbapenemase-producing . Culture-based approaches have been relied on over the past decades as the method of choice for the early detection of gut colonization by MDR Gram-negative bacteria. However, various studies have indicated its limited sensitivity, underlining the need for new screening procedures in onco-hematological patients. Here, we evaluated a shotgun metagenomics approach to detect ESBL- and/or carbapenemase-producing in the gut of 28 patients who had recovered from AL, which were previously colonized by these bacteria but cured at the time of sampling, as judged by culture-based methods. No ESBL or carbapenemase determinants were detected among the many resistance genes found by the metagenomics approach, supporting that patients were truly decolonized, with considerable consequences for their future clinical management. Due to the relatively low number of patients available for the present investigation, further studies should be conducted to support the utility and applicability of metagenomics for the routine screening of MDR bacteria in onco-hematological patients.

摘要

被诊断患有急性白血病(AL)的患者免疫系统较弱。这些患者获得的感染令人担忧,当涉及革兰氏阴性多重耐药(MDR)细菌时尤其令人担忧,因为它们难以治疗,尤其是在产生超广谱β-内酰胺酶(ESBL)和/或碳青霉烯酶的情况下。在过去几十年中,基于培养的方法一直是早期检测肠道中MDR革兰氏阴性菌定植的首选方法。然而,各种研究表明其敏感性有限,这突出表明肿瘤血液学患者需要新的筛查程序。在这里,我们评估了一种鸟枪法宏基因组学方法,以检测28例从AL康复的患者肠道中产生ESBL和/或碳青霉烯酶的情况,这些患者以前被这些细菌定植,但根据基于培养的方法判断,在采样时已治愈。在宏基因组学方法发现的众多耐药基因中未检测到ESBL或碳青霉烯酶决定簇,这支持患者确实已被清除定植,这对他们未来的临床管理有重大影响。由于本研究可用的患者数量相对较少,应进行进一步研究以支持宏基因组学在肿瘤血液学患者中常规筛查MDR细菌的实用性和适用性。