[Phenotypic and genotypic characterization of probiotic bacterial strains used in medicinal products].

Aldona Wiatrzyk, Maciej Polak, Urszula Czajka, Katarzyna Krysztopa-Grzybowska, Anna Lutyńska
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Abstract

Introduction: The optimization of quality testing strategy of products containing probiotics might allow to general improvement of its safer use in humans. The goal of the study was the evaluation of quality expressed by identity, colony forming unit (CFU) and antibiotic sensitivity ofprobiotics used in medicinal products available in Poland using the appropriate and validated procedures.

Methods: The medicinal products containing L. rhamnosus, L. acidophilus, L. delbrueckii subsp. bulgaricus and B. animalis subsp. lactis, L. helveticus, and L. gasseri were tested for species identity performed with validated rep-PCR (BOXA 1R) method. The antimicrobial susceptibility of working seeds and strains isolated to 26 antibiotics were tested by disk diffusion and E-test methods using relevant references as recommended by EUCAST. The numbers of probiotic strains, expressed as cfu count per package, was done using plating plunge method.

Results: All strains tested, except B. lactis, were found to be resistant to trimethoprim-sulphamethoxazole, nalidixic acid, metronidazole, and colistin. B. lactis was resistant to aminoglycosides. L. rhamnosus strains were found to be resistant to vancomycin, (MIC > 256 microg/ml) similarly to ATCC strains (L. rhamnosus GG 53103 and 244). The sensitivity to other antibiotics was strain specific. The rep-PCR method was found species and strain specific. All products tested fulfilled declared countent as measured by cfu count/package.

Conclusions: Quality of medicinal products containing probiotics was found undoubted and confirmed. The optimized strategy of quality monitoring of probiotics used in medicinal products can be used in dietary supplements and foodstuffs intended for particular nutritional uses.

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[药用产品中使用的益生菌菌株的表型和基因型表征]。
前言:优化含益生菌产品的质量检测策略可能会使其在人体中的安全性得到普遍提高。该研究的目的是通过使用适当和经过验证的程序,对波兰可用的医药产品中使用的益生菌的特性、菌落形成单位(CFU)和抗生素敏感性进行质量评价。方法:药材中含有鼠李糖乳杆菌、嗜酸乳杆菌、德尔布鲁氏乳杆菌亚种。保加利亚芽孢杆菌和动物芽孢杆菌亚种。采用已验证的rep-PCR (BOXA 1R)方法对lactis、L. helveticus和L. gasseri进行物种鉴定。根据EUCAST推荐的相关文献,采用纸片扩散法和E-test法检测工作种子和菌株对26种抗生素的敏感性。以每包cfu数表示的益生菌菌种数,采用镀槽法测定。结果:除乳酸菌外,所有菌株均对甲氧苄啶-磺胺甲恶唑、萘啶酸、甲硝唑和粘菌素耐药。乳酸菌对氨基糖苷类有抗药性。鼠李糖乳杆菌对万古霉素的耐药程度与ATCC菌株(鼠李糖乳杆菌GG 53103和244)相似(MIC > 256 μ g/ml)。对其他抗生素的敏感性是菌株特异性的。rep-PCR方法具有种特异性和菌株特异性。所有测试产品均符合cfu计数/包装的声明含量。结论:发现含益生菌制剂的药品质量是不容置疑和肯定的。医药产品中益生菌质量监测的优化策略可用于膳食补充剂和特定营养用途的食品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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