Mao Xin-Ru, Wang Rui-Cheng, Li Rong-Jiao, Zhou Cai-Rong, Chen Xian-Kai, Cheng Can-Can, Yin Xiao-Mao
Clinical Laboratory, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Clinical Laboratory, Zhongshan Guzhen People's Hospital, Zhongshan, China.
Can J Infect Dis Med Microbiol. 2020 Jul 2;2020:1391698. doi: 10.1155/2020/1391698. eCollection 2020.
Culture is still the gold standard for the detection of genital mycoplasma which could cause urogenital infections in humans. Mycoplasma IST2 is a commercial kit widely used for the detection of and species. Its accuracy was partially impaired because clinical specimens are usually mixed with purulent or transparent mucus. We aimed to solve this problem through sample homogenization by -acetylcysteine (NAC) treatment.
Twenty-two endocervical swab samples were collected from 22 female patients with suspected mycoplasma infection, while 11 of these specimens were with purulent or transparent mucus. Mycoplasma IST2 testing kit was used for mycoplasma culture and AST for the control group and NAC-treated group.
Genital mycoplasma was detected in 15 of 22 samples for both groups. The colony number in 6 out of 11 purulent specimens (54.5%) was more than 10 CFU/ml of genital mycoplasma for the NAC-treated group, while only one of 11 (9.1%) for the control group. For the nonpurulent specimens, no significant difference had been found in colony counting of genital mycoplasma between the control group and NAC-treated group ( > 0.05). The results of antimicrobial susceptibility testing for the NAC-treated group were highly similar to those for the control group.
Our results demonstrate that NAC is helpful in sample homogenization and NAC treatment can improve the detection efficiency of mycoplasma with Mycoplasma IST2 testing.
培养仍然是检测可导致人类泌尿生殖系统感染的生殖支原体的金标准。Mycoplasma IST2是一种广泛用于检测[具体物种1]和[具体物种2]的商业试剂盒。由于临床标本通常与脓性或透明黏液混合,其准确性受到一定影响。我们旨在通过用N - 乙酰半胱氨酸(NAC)处理使样本均匀化来解决这一问题。
从22例疑似支原体感染的女性患者中采集22份宫颈拭子样本,其中11份标本带有脓性或透明黏液。Mycoplasma IST2检测试剂盒用于支原体培养,对照组和NAC处理组均进行AST检测。
两组22份样本中均有15份检测到生殖支原体。NAC处理组11份脓性标本中有6份(54.5%)的生殖支原体菌落数超过10 CFU/ml,而对照组1份(9.1%)。对于非脓性标本,对照组和NAC处理组之间生殖支原体菌落计数无显著差异(P>0.05)。NAC处理组的抗菌药物敏感性测试结果与对照组高度相似。
我们的结果表明NAC有助于样本均匀化,NAC处理可提高使用Mycoplasma IST2检测支原体的检测效率。