Rowe Ryan A, Stephenson Ryan M, East Destry L, Wright Scott
Clinical Laboratory Science Program, Department of Health Professions, Weber State University, Ogden, UT 84408-3905, USA.
Clin Lab Sci. 2009 Winter;22(1):39-44.
The purpose of this study was to (1) determine the rates of penicillin and erythromycin resistance among Streptococcus pyogenes isolates in northern Utah, and (2) determine the genotype of the erythromycin resistant strains, thereby providing information regarding the mechanism of the resistance.
Seven hundred thirty-nine isolates of S. pyogenes were identified on 5% Sheep Blood Agar. Susceptibility to erythromycin and penicillin was performed using Muller-Hinton blood agar. All isolates resistant to erythromycin were then genotyped using PCR primers specific to one of the following: mefA gene, indicating the mechanism of resistance was an efflux pump; ermA gene, in which the mechanism was inducible methylation of the ribosomes; and ermB indicating constitutive methylation of the ribosomes.
This study was conducted at Weber State University, in the Department of Clinical Laboratory Sciences.
Samples were collected from 9 clinics ranging from North Ogden to Taylorsville, Utah. All samples were previously tested positive for S. pyogenes by the clinic from where the samples were collected.
Of the 739 S. pyogenes isolates tested, 2.4% were resistant to erythromycin with no resistance observed to penicillin. Of the strains that displayed some degree of resistance, the gene frequencies observed were as follows: 48.1% mefA, 26.0% ermA, 3.7% ermB, and 22.2% multiple genes.
The most common genotype was mefA, indicating that the efflux pump (M phenotype) is the most common mechanism in the surveyed area, followed by ermA, which produces the inducible methylating enzyme. A significant number of isolates was also observed to express both the efflux pump and the constitutive methylating enzyme.
本研究的目的是:(1)确定犹他州北部化脓性链球菌分离株中青霉素和红霉素的耐药率,以及(2)确定红霉素耐药菌株的基因型,从而提供有关耐药机制的信息。
在5%绵羊血琼脂上鉴定出739株化脓性链球菌。使用Muller-Hinton血琼脂检测对红霉素和青霉素的敏感性。然后使用针对以下之一的PCR引物对所有对红霉素耐药的分离株进行基因分型:mefA基因,表明耐药机制是外排泵;ermA基因,其机制是核糖体的诱导性甲基化;ermB表明核糖体的组成性甲基化。
本研究在韦伯州立大学临床检验科学系进行。
样本从犹他州北奥格登到泰勒维尔的9家诊所收集。所有样本之前在所收集样本的诊所被检测出化脓性链球菌呈阳性。
在检测的739株化脓性链球菌分离株中,2.4%对红霉素耐药,未观察到对青霉素耐药。在表现出一定程度耐药的菌株中,观察到的基因频率如下:mefA为48.1%,ermA为26.0%,ermB为3.7%,多个基因占22.2%。
最常见的基因型是mefA,表明外排泵(M表型)是调查区域中最常见的耐药机制,其次是ermA,它产生诱导性甲基化酶。还观察到大量分离株同时表达外排泵和组成性甲基化酶。