Miyagi Chika, Yamane Nobuhisa, Yogesh Bhusal, Ano Hiromi, Takashima Tetsuya
Department of Laboratory Medicine, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan.
Diagn Microbiol Infect Dis. 2004 Feb;48(2):111-6. doi: 10.1016/j.diagmicrobio.2003.09.013.
The pncA gene mutations associated with pyrazinamide (PZA) resistance in Mycobacterium tuberculosis complex were determined in 26 PZA-resistant isolates in Japan. Of the 26 PZA-resistant isolates included, 21 were negative for pyrazinamidase (PZase). Of these, 20 isolates had various pncA mutations, resulting in alteration of primary amino acid sequence. However, 1 PZase-negative isolate did not have any mutation on pncA gene. The remaining 5 PZA-resistant isolates were positive for PZase and had identical pncA alleles with PZA-susceptible isolates. IS6110 RFLP analysis demonstrated various distinct IS6110 types and 5 pairs of isolates were very close to each other (>90% identical pattern). This study demonstrates that most of the PZA resistance is a result of various mutations on pncA resulting in loss of PZase activity. Further investigation, particularly on PZase-positive but PZA-resistant isolates and a PZase-negative isolate with no mutation on pncA, should be urgently done.
在日本的26株对吡嗪酰胺(PZA)耐药的结核分枝杆菌复合群菌株中,测定了与PZA耐药相关的pncA基因突变情况。在纳入的26株PZA耐药菌株中,21株的吡嗪酰胺酶(PZase)检测呈阴性。其中,20株分离株存在各种pncA突变,导致一级氨基酸序列改变。然而,1株PZase阴性分离株的pncA基因未发生任何突变。其余5株PZA耐药分离株的PZase检测呈阳性,且其pncA等位基因与PZA敏感分离株相同。IS6110限制性片段长度多态性(RFLP)分析显示出各种不同的IS6110类型,并且有5对分离株彼此非常相似(>90%相同模式)。本研究表明,大多数PZA耐药是由pncA上的各种突变导致PZase活性丧失所致。应立即开展进一步调查,特别是针对PZase阳性但PZA耐药的分离株以及pncA无突变的PZase阴性分离株。