1 Department of Zoology, University of British Columbia, Vancouver, Canada.
4 Division of Brain and Therapeutics, Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
J Med Microbiol. 2019 Jun;68(6):952-956. doi: 10.1099/jmm.0.001001. Epub 2019 May 20.
Exploiting the immunosuppressive, analgesic and highly addictive properties of morphine could increase the success of a bacterial pathogen. Therefore, we performed sequence similarity searches for two morphine biosynthesis demethylases in bacteria. For thebaine 6-O-demethylase and codeine O-demethylase, we found strong alignments to three (Pseudomonas aeruginosa, Klebsiella pneumoniae and Acinetobacter baumannii) of the six ESKAPE pathogens (Enterococcus faecalis, Staphylococcus aureus, K. pneumoniae, A. baumannii, P. aeruginosa and Enterobacter species) that are commonly associated with drug resistance and nosocomial infections. Expression of the aligned sequence found in P. aeruginosa (NP_252880.1/PA4191) is upregulated in isolates obtained from cystic fibrosis patients. Our findings provide putative mechanistic targets for understanding the role of morphine in pathogenicity.
利用吗啡的免疫抑制、镇痛和高度成瘾特性可能会增加细菌病原体的成功率。因此,我们在细菌中搜索了两种吗啡生物合成去甲基酶的序列相似性。对于蒂巴因 6-O-去甲基酶和可待因 O-去甲基酶,我们发现与六种 ESKAPE 病原体(粪肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、铜绿假单胞菌和肠杆菌属)中的三种(铜绿假单胞菌、肺炎克雷伯菌和鲍曼不动杆菌)有很强的排列一致性,这些病原体通常与耐药性和医院获得性感染有关。在从囊性纤维化患者中获得的分离物中,发现排列在铜绿假单胞菌(NP_252880.1/PA4191)中的序列的表达上调。我们的发现为理解吗啡在致病性中的作用提供了可能的机制靶标。