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首页> 外文期刊>Journal of Clinical Microbiology >Immunoblot Method To Detect Streptococcus pneumoniae and Identify Multiple Serotypes from Nasopharyngeal Secretions
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Immunoblot Method To Detect Streptococcus pneumoniae and Identify Multiple Serotypes from Nasopharyngeal Secretions

机译:免疫印迹法检测肺炎链球菌并从鼻咽分泌物中鉴定出多种血清型

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Conventional culture techniques are limited in the ability to detect multiple Streptococcus pneumoniae serotypes in nasopharyngeal (NP) secretions. We developed an immunoblot (IB) method with monoclonal antibodies (MAbs) to detect S. pneumoniae and to identify serotypes. NP specimens stored in skim milk-tryptone-glucose-glycerol medium were assessed by the IB method and the reference culture method (RM). In the RM, four optochin-sensitive alpha-hemolytic colonies resembling pneumococci were typed by the Quellung reaction. In the IB method, a nitrocellulose membrane blot of surface growth was reacted with a pneumococcal surface adhesion (PsaA) MAb and visualized. Of 47 NP specimens, 32 (68%) were found to be positive and 13 (28%) were found to be negative for pneumococci by both methods; each method alone yielded one positive result. The sensitivity and specificity of the IB method for the detection of pneumococci were 97 and 93%, respectively. To identify serotypes, blots were tested with serotype-specific MAbs (4, 6A, 6B, 9V, 14, 18C, 19F, and 23F). To detect the remaining serotypes, positive serotype-specific replicate blots were compared visually to an original anti-PsaA-positive blot; four unidentified colonies were subcultured and serotyped by the Quellung reaction. Fifty-eight S. pneumoniae-positive NP specimens containing 69 pneumococcal strains (23 serotypes) were tested; 68 (98.6%) of the strains were detected by the IB method, and 66 (95.6%) were detected by the RM. For 11 specimens found to contain two serotypes, both methods detected both serotypes in 7 (63.6%), the IB method alone detected the two serotypes in 3 (27.3%), and the RM alone detected both serotypes in 1 (9%). The IB method identified multiple clones and minor populations of pneumococci in NP secretions. This method is useful for detecting specific serotypes and carriage of multiple serotypes in epidemiologic surveillance and carriage studies.
机译:传统的培养技术在检测鼻咽(NP)分泌物中多种肺炎链球菌血清型的能力上受到限制。我们开发了一种使用单克隆抗体(MAb)的免疫印迹(IB)方法来检测 S。肺炎并鉴定血清型。通过IB法和参考培养法(RM)对存储在脱脂奶-rypto-葡萄糖-甘油培养基中的NP标本进行了评估。在RM中,通过Quellung反应分出了四个类似肺炎球菌的视光敏菌敏感的α-溶血菌落。在IB方法中,使表面生长的硝酸纤维素膜印迹与肺炎球菌表面粘附(PsaA)MAb反应并可视化。两种方法在47个NP标本中,肺炎球菌均为32例(68%)为阳性,而13例(28%)为阴性。每种方法单独产生一个积极的结果。 IB法检测肺炎球菌的敏感性和特异性分别为97%和93%。为了鉴定血清型,用血清型特异性MAb(4、6A,6B,9V,14、18C,19F和23F)测试印迹。为了检测剩余的血清型,将阳性的血清型特异性复制印迹与原始的抗PsaA阳性印迹进行目测比较;通过Quellung反应对4个身份不明的菌落进行亚培养和血清分型。 58.S.肺炎链球菌阳性NP标本含有69个肺炎球菌菌株(23种血清型)。 IB法检出68株(98.6%),RM检出66株(95.6%)。对于发现包含两种血清型的11个标本,两种方法都检测到7种血清型(63.6%),仅IB方法仅检测到3种血清型(27.3%),而RM单独检测到1种血清型(9%)。 IB方法鉴定了NP分泌物中的肺炎球菌的多个克隆和少量群体。该方法可用于在流行病学监测和运输研究中检测特定的血清型和多种血清型的运输。

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