The Gonococcus fights back: is this time a knock out?

被引:120
作者
Lewis, David A. [1 ,2 ,3 ]
机构
[1] Natl Hlth Lab Serv, Natl Inst Communicable Dis, STI Reference Ctr, Johannesburg, South Africa
[2] Univ Witwatersrand, Fac Hlth Sci, Dept Internal Med, Johannesburg, South Africa
[3] Univ Cape Town, Div Med Microbiol, ZA-7925 Cape Town, South Africa
关键词
RESISTANT NEISSERIA-GONORRHOEAE; PENICILLIN-BINDING PROTEIN-2; MEDIATED ANTIBIOTIC-RESISTANCE; MOSAIC-LIKE STRUCTURE; HIGH-LEVEL; REDUCED SUSCEPTIBILITY; ANTIMICROBIAL SUSCEPTIBILITY; DECREASED SUSCEPTIBILITY; TETRACYCLINE-RESISTANCE; AMINO-ACID;
D O I
10.1136/sti.2010.042648
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Since the introduction of antibiotics in the 1930s, Neisseria gonorrhoeae has exhibited a remarkable ability to acquire novel genetic resistance determinants. Initially, sulphonamides were replaced by penicillin, while tetracyclines were prescribed for penicillin-allergic patients. With the advent of penicillinase-producing gonococci, spectinomycin was only briefly useful as alternative treatment and plasmid-mediated tetracycline resistance spread rapidly from the mid-1980s onwards. The fluoroquinolones followed but chromosomally mediated resistance appeared after only a decade of use. Seventy years on, we now face a global public health challenge of immense significance-the emergence of resistance to cephalosporins. With lack of investment in the search for new anti-gonococcal antimicrobial agents or vaccine research, the global spread of multiresistant gonococci can be seen. The impact of untreatable gonorrhoea on HIV transmission could be enormous in high-prevalence countries. This threat comes at a time when many national STI control programmes are weak. To delay the emergence of extensively drug-resistant gonorrhoea, public health systems require strengthening and novel strategies need implementing to enhance the therapeutic lifespan of the few antimicrobial agents that we have left.
引用
收藏
页码:415 / 421
页数:7
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