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新型链球菌乳胶分组试剂盒的评估

Evaluation of new streptococcal latex grouping kit.

作者信息

Vicca A F, Stansfield R E, Masterton R G

机构信息

Central Microbiological Laboratories, Western General Hospital, Edinburgh.

出版信息

J Clin Pathol. 1993 Jan;46(1):79-80. doi: 10.1136/jcp.46.1.79.

Abstract

AIMS

To evaluate a new streptococcal latex grouping kit (Shield Diagnostics Ltd) and compare it against an established latex agglutination method (Streptex; Wellcome Diagnostics).

METHODS

Two hundred and forty seven strains of streptococci and enterococci were tested with each kit by one operator and according to the manufacturer's instructions. Strains failing to group or giving discordant results were identified to species level.

RESULTS

Two discrepant grouping results were observed and 13 non-beta haemolytic streptococci failed to group with either product. The Shield kit successfully identified 232 isolates at 15 minutes of enzyme extraction incubation compared with 224 and 233 on short (15 minutes) and long (1 hour) incubations, respectively, for Streptex (p > 0.23 for both comparisons). On short incubation only, the Shield kit detected significantly more strains of Enterococcus faecium (p = 0.007). The reaction strengths were similar for both kits (p > 0.16). No cross-reactions were observed but the Streptex kit produced significantly fewer tests with visible granularity (p < 0.003).

CONCLUSIONS

Although the Shield product appeared to detect group D antigen more readily, overall no important differences in performance were observed. Prospective users of the new method should first become familiar with its characteristics.

摘要

目的

评估一种新型链球菌乳胶分组试剂盒(Shield Diagnostics Ltd),并将其与一种既定的乳胶凝集方法(Streptex;Wellcome Diagnostics)进行比较。

方法

由一名操作人员按照制造商的说明,使用每种试剂盒对247株链球菌和肠球菌进行检测。对未能分组或结果不一致的菌株进行种属鉴定。

结果

观察到两个分组结果不一致的情况,13株非β溶血性链球菌用两种产品均未能分组。与Streptex相比,Shield试剂盒在酶提取孵育15分钟时成功鉴定出232株分离株,Streptex在短(15分钟)孵育和长(1小时)孵育时分别鉴定出224株和233株(两种比较的p值均>0.23)。仅在短孵育时,Shield试剂盒检测到的粪肠球菌菌株明显更多(p = 0.007)。两种试剂盒的反应强度相似(p>0.16)。未观察到交叉反应,但Streptex试剂盒产生可见颗粒的检测显著更少(p < 0.003)。

结论

虽然Shield产品似乎更容易检测到D群抗原,但总体上未观察到性能上的重要差异。新方法的潜在用户应首先熟悉其特性。

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