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耐(linezolid)ST36 型甲氧西林耐药金黄色葡萄球菌与两名儿科囊性纤维化患者长时间(linezolid)治疗相关。

Linezolid-resistant ST36 methicillin-resistant Staphylococcus aureus associated with prolonged linezolid treatment in two paediatric cystic fibrosis patients.

机构信息

Centre for Infections, Health Protection Agency, 61 Colindale Avenue, London NW9 5EQ, UK.

出版信息

J Antimicrob Chemother. 2010 Mar;65(3):442-5. doi: 10.1093/jac/dkp494. Epub 2010 Jan 20.

DOI:10.1093/jac/dkp494
PMID:20089543
Abstract

OBJECTIVES

To describe the emergence of linezolid-resistant methicillin-resistant Staphylococcus aureus (MRSA) of sequence type (ST)36 lineage in two paediatric patients with cystic fibrosis, after long-term low-dose linezolid treatment.

METHODS

Two paediatric males with cystic fibrosis had sputum samples quantitatively cultured during hospitalization. After the isolation of MRSA from both patients, oral treatment with 300 mg linezolid twice daily was initiated for periods of 1-2 months separated by up to 6 months. Isolates cultured 9 months after the start of treatment were tested for resistance to linezolid by agar dilution (BSAC). Resistant isolates were examined for 23S rDNA mutations, and typed by phage and macrorestriction with SmaI. Isolates from follow-up sputum samples were obtained until 44-51 months after treatment with linezolid.

RESULTS

Colonization with MRSA was at a density of approximately 10(6) cfu/mL sputum for both subjects. Initial isolates were susceptible to linezolid, but, 9 months later, isolates from both patients were resistant (MICs > 16 mg/L). Both isolates were epidemic MRSA-16 variant A1 (ST36-MRSA-II), which is widespread in UK hospitals. Both isolates were heterozygous for a G2576T mutation in their 23S rDNA genes, but one was resistant to fusidic acid and tetracycline. In follow-up sampling, the younger patient yielded linezolid-resistant EMRSA-16 for a further 42 months, whilst the other lost the linezolid-resistant MRSA and had alternately Pseudomonas aeruginosa or linezolid-susceptible EMRSA-16 variant A1 isolated over 35 further months.

CONCLUSIONS

Linezolid resistance emerged in two isolates of ST36 MRSA colonizing the lungs of two paediatric cystic fibrosis patients. Subtherapeutic levels of linezolid may have facilitated the selection of resistance.

摘要

目的

描述两例长期低剂量利奈唑胺治疗的囊性纤维化患儿中,耐甲氧西林金黄色葡萄球菌(MRSA)ST36 谱系出现利奈唑胺耐药的情况。

方法

两名患有囊性纤维化的儿科男性患者在住院期间定量培养痰样本。从两名患者中分离出 MRSA 后,开始口服利奈唑胺 300mg,每日两次,疗程为 1-2 个月,间隔最长 6 个月。在治疗开始后 9 个月培养的分离物用琼脂稀释法(BSAC)检测利奈唑胺耐药性。对耐药分离物进行 23S rDNA 突变检测,并通过噬菌体和 SmaI 宏限制型进行分型。在利奈唑胺治疗后 44-51 个月获得随访痰样本中的分离物。

结果

两名患者的痰液中 MRSA 定植密度约为 10(6)cfu/mL。初始分离物对利奈唑胺敏感,但 9 个月后,两名患者的分离物均耐药(MICs>16mg/L)。两种分离物均为流行的英国医院广泛存在的 MRSA-16 变异 A1(ST36-MRSA-II)。两种分离物的 23S rDNA 基因均存在 G2576T 点突变,但其中一种对夫西地酸和四环素耐药。在后续采样中,年龄较小的患者在进一步的 42 个月内产生了利奈唑胺耐药的 EMRSA-16,而另一名患者则失去了利奈唑胺耐药的 MRSA,并在 35 个月以上的时间交替分离出铜绿假单胞菌或利奈唑胺敏感的 EMRSA-16 变异 A1。

结论

ST36 MRSA 的两种分离物在两名囊性纤维化患儿的肺部定植,出现了利奈唑胺耐药性。利奈唑胺的亚治疗水平可能促进了耐药性的选择。

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