Wang Q, Xia S Y, Long J Q
Naval Medical Institute, Shanghai.
Zhonghua Liu Xing Bing Xue Za Zhi. 1996 Dec;17(6):350-2.
Mycoplasma DNA in nasopharynx secretion from seventy pediatric mycoplasma cases was detected, using rapid feit of PCR DNA sample preparation method and simple PCR processes. The result of PCR showed that: fifty-three positive cases with a positive rate 75.7%, comparing with only 53.8% positive rate using mycoplasma culture method (P < 0.05). Thirteen PCR positive patients were treated by Venoclysis Erythromycin for 10-14 days but mycoplasma DNA was identified by PCR again. Among them, eight cases turned negative, but five cases still remained positive. The resalt showed that this method was not only more sensitive and reliable than conventional culture techniques, but also could simplify the PCR processes. It could be used for routine mycoplasma pneumonia test and for early diagnosis, which leads to early treatment and evaluation of therapeufic effect.
采用快速的PCR DNA样本制备方法和简单的PCR程序,对70例小儿支原体病例的鼻咽分泌物中的支原体DNA进行检测。PCR结果显示:53例阳性病例,阳性率为75.7%,而支原体培养法的阳性率仅为53.8%(P<0.05)。13例PCR阳性患者静脉滴注红霉素治疗10 - 14天,之后再次用PCR鉴定支原体DNA。其中,8例转阴,但5例仍为阳性。结果表明,该方法不仅比传统培养技术更灵敏可靠,而且能简化PCR程序。可用于支原体肺炎的常规检测及早期诊断,从而实现早期治疗和疗效评估。