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
相关论文
共 114 条
[1]   Mosaic-like structure of penicillin-binding protein 2 gene (PenA) in clinical isolates of Neissetia gonorrhoeae with reduced susceptibility to cefixime [J].
Ameyama, S ;
Onodera, S ;
Takahata, M ;
Minami, S ;
Maki, N ;
Endo, K ;
Goto, H ;
Suzuki, H ;
Oishi, Y .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (12) :3744-3749
[2]  
ASHFORD WA, 1981, LANCET, V2, P1035
[3]   TRIMETHOPRIM-SULFAMETHOXAZOLE IN TREATMENT OF GONOCOCCAL URETHRITIS - CLINICAL AND LABORATORY CORRELATES [J].
AUSTIN, TW ;
BROOKS, GF ;
BETHEL, M ;
ROBERTS, FL ;
TURCK, M ;
HOLMES, KK .
JOURNAL OF INFECTIOUS DISEASES, 1973, 128 :S666-S672
[4]  
Barry PM, 2009, EXPERT OPIN PHARMACO, V10, P555, DOI [10.1517/14656560902731993, 10.1517/14656560902731993 ]
[5]   NEISSERIA-GONORRHOEAE ACQUIRES MUTATIONS IN ANALOGOUS REGIONS OF GYRA AND PARC IN FLUOROQUINOLONE-RESISTANT ISOLATES [J].
BELLAND, RJ ;
MORRISON, SG ;
ISON, C ;
HUANG, WM .
MOLECULAR MICROBIOLOGY, 1994, 14 (02) :371-380
[6]  
BERG SW, 1981, SEX TRANSM DIS, V8, P38
[7]   EFFECT OF SPECTINOMYCIN USE ON THE PREVALENCE OF SPECTINOMYCIN-RESISTANT AND OF PENICILLINASE-PRODUCING NEISSERIA-GONORRHOEAE [J].
BOSLEGO, JW ;
TRAMONT, EC ;
TAKAFUJI, ET ;
DINIEGA, BM ;
MITCHELL, BS ;
SMALL, JW ;
KHAN, WN ;
STEIN, DC .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (05) :272-278
[8]   INSERTION OF AN EXTRA AMINO-ACID IS THE MAIN CAUSE OF THE LOW AFFINITY OF PENICILLIN-BINDING PROTEIN-2 IN PENICILLIN-RESISTANT STRAINS OF NEISSERIA-GONORRHOEAE [J].
BRANNIGAN, JA ;
TIRODIMOS, IA ;
ZHANG, QY ;
DOWSON, CG ;
SPRATT, BG .
MOLECULAR MICROBIOLOGY, 1990, 4 (06) :913-919
[9]   A NOVEL GONOCOCCAL BETA-LACTAMASE PLASMID [J].
BRETT, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1989, 23 (04) :653-654
[10]   Neisseria gonorrhoeae Antimicrobial Susceptibility in Lilongwe, Malawi, 2007 [J].
Brown, Lillian B. ;
Krysiak, Robert ;
Kamanga, Gift ;
Mapanje, Clemente ;
Kanyamula, Happiness ;
Banda, Blessings ;
Mhango, Chisale ;
Hoffman, Mariah ;
Kamwendo, Debbie ;
Hobbs, Marcia ;
Hosseinipour, Mina C. ;
Martinson, Francis ;
Cohen, Myron S. ;
Hoffman, Irving F. .
SEXUALLY TRANSMITTED DISEASES, 2010, 37 (03) :169-172