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1997/1998年和2002/2003年期间欧洲产β-内酰胺酶和不产β-内酰胺酶的流感嗜血杆菌分离株的药敏性

Susceptibility of European beta-lactamase-positive and -negative Haemophilus influenzae isolates from the periods 1997/1998 and 2002/2003.

作者信息

Fluit A C, Florijn A, Verhoef J, Milatovic D

机构信息

Eijkman-Winkler Center, University Medical Center Utrecht, The Netherlands.

出版信息

J Antimicrob Chemother. 2005 Jul;56(1):133-8. doi: 10.1093/jac/dki167. Epub 2005 May 25.

Abstract

AIMS

To test prospectively the activity of cefixime and comparators against Haemophilus influenzae from Europe and to compare the susceptibilities of isolates from 1997/1998 with isolates from 2002/2003 paying special attention to the epidemiology of amoxicillin resistance.

METHODS

MICs of antibiotics were determined using broth microdilution. For beta-lactamase-negative isolates with reduced susceptibility to amoxicillin, the nucleotide sequence of the penicillin-binding domain of PBP3 was determined.

RESULTS

The prevalence of beta-lactamase-positive isolates in certain countries has reached 38%. During the period 1997/1998, 8.8% of the isolates were beta-lactamase-negative and non-susceptible to amoxicillin (BLNAR). During the period 2002/2003, 9.6% of the isolates were BLNAR. The emergence of the BLNAR phenotype of H. influenzae was demonstrated in all countries with a prevalence ranging from 2% to 20%. The penicillin-binding domain of PBP3 from 30 sequenced isolates showed known amino acid substitutions, although no amino acid changes were observed in two BLNAR isolates. Clonal spread of BLNAR strains was limited or absent in our study. Both beta-lactamase-producing and BLNAR strains of H. influenzae were fully susceptible to cefixime. However, neither beta-lactamase-producing nor BLNAR isolates were fully susceptible to the other cephalosporins tested. All isolates were also fully susceptible to levofloxacin, moxifloxacin, azithromycin and telithromycin.

CONCLUSIONS

The prevalence of the BLNAR phenotype in Europe is increasing, but no new amino acid substitutions were detected in the penicillin-binding domain of PBP3. Cefixime remains a useful treatment option for respiratory tract infections, including in areas with increasing resistance problems.

摘要

目的

前瞻性地测试头孢克肟及对照药物对来自欧洲的流感嗜血杆菌的活性,并比较1997/1998年分离株与2002/2003年分离株的敏感性,特别关注阿莫西林耐药的流行病学情况。

方法

采用肉汤微量稀释法测定抗生素的最低抑菌浓度(MIC)。对于对阿莫西林敏感性降低的β-内酰胺酶阴性分离株,测定青霉素结合蛋白3(PBP3)青霉素结合结构域的核苷酸序列。

结果

某些国家β-内酰胺酶阳性分离株的流行率已达38%。在1997/1998年期间,8.8%的分离株为β-内酰胺酶阴性且对阿莫西林不敏感(BLNAR)。在2002/2003年期间,9.6%的分离株为BLNAR。在所有国家均证实了流感嗜血杆菌BLNAR表型的出现,流行率在2%至20%之间。对30株测序分离株的PBP3青霉素结合结构域进行分析,发现了已知的氨基酸替代,不过在两株BLNAR分离株中未观察到氨基酸变化。在我们的研究中,BLNAR菌株的克隆传播有限或不存在。产β-内酰胺酶和BLNAR的流感嗜血杆菌菌株对头孢克肟均完全敏感。然而,产β-内酰胺酶和BLNAR的分离株对所测试的其他头孢菌素均不完全敏感。所有分离株对左氧氟沙星、莫西沙星、阿奇霉素和泰利霉素也均完全敏感。

结论

欧洲BLNAR表型的流行率正在上升,但在PBP3的青霉素结合结构域未检测到新的氨基酸替代。头孢克肟仍然是治疗呼吸道感染的有用选择,包括在耐药问题日益严重的地区。

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