PCR and restriction endonuclease assay for detection of a novel mutation associated with sulfonamide resistance in Neisseri meningitidis

被引:6
作者
Bennett, DE
Cafferkey, MT
机构
[1] Childrens Univ Hosp, Epidemiol & Mol Biol Unit, Dublin 1, Ireland
[2] Royal Coll Surgeons Ireland, Dept Clin Microbiol, Dublin 2, Ireland
关键词
D O I
10.1128/AAC.47.10.3336-3338.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We identified a previously undocumented mutation in the dihydropteroate synthase (folP) gene associated with Neisseria meningitidis sulfonamide resistance. A PCR-based assay to detect this mutation, which is 100% predictive of sulfonamide resistance, was developed.
引用
收藏
页码:3336 / 3338
页数:3
相关论文
共 17 条
[1]   Clonal distribution of invasive Neisseria meningitidis isolates from the Norwegian county of Telemark, 1987 to 1995 [J].
Aakre, RK ;
Jenkins, A ;
Kristiansen, BE ;
Froholm, LO .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (09) :2623-2628
[2]   Crystal structure of the anti-bacterial sulfonamide drug target dihydropteroate synthase [J].
Achari, A ;
Somers, DO ;
Champness, JN ;
Bryant, PK ;
Rosemond, J ;
Stammers, DK .
NATURE STRUCTURAL BIOLOGY, 1997, 4 (06) :490-497
[3]  
Allunans J, 2001, SCAND J INFECT DIS, V33, P516, DOI 10.1080/00365540110026610
[4]   MORTALITY IN MENINGOCOCCAL INFECTIONS [J].
ANDERSEN, BM .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1978, 10 (04) :277-282
[5]   ENDOTOXIN RELEASE FROM INVASIVE MENINGOCOCCI RELATED TO SULFONAMIDE RESISTANCE, SEROGROUP AND SEROTYPE [J].
ANDERSEN, BM ;
SOLBERG, O ;
HOLTEN, E .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1987, 19 (01) :43-49
[6]   Crystal structure of Mycobacterium tuberculosis 6-hydroxymethyl-7,8-dihydropteroate synthase in complex with pterin monophosphate:: New insight into the enzymatic mechanism and sulfa-drug action [J].
Baca, AM ;
Sirawaraporn, R ;
Turley, S ;
Sirawaraporn, W ;
Hol, WGJ .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 302 (05) :1193-1212
[7]  
BOVRE K, 1980, NIPH (National Institute of Public Health) Annals (Oslo), V3, P9
[8]   Adaptation to sulfonamide resistance in Neisseria meningitidis may have required compensatory changes to retain enzyme function: Kinetic analysis of dihydropteroate synthases from N-meningitidis expressed in a knockout mutant of Escherichia coli [J].
Fermer, C ;
Swedberg, G .
JOURNAL OF BACTERIOLOGY, 1997, 179 (03) :831-837
[9]   SULFONAMIDE RESISTANCE IN NEISSERIA-MENINGITIDIS AS DEFINED BY SITE-DIRECTED MUTAGENESIS COULD HAVE ITS ORIGIN IN OTHER SPECIES [J].
FERMER, C ;
KRISTIANSEN, BE ;
SKOLD, O ;
SWEDBERG, G .
JOURNAL OF BACTERIOLOGY, 1995, 177 (16) :4669-4675
[10]   Structure and function of the dihydropteroate synthase from Staphylococcus aureus [J].
Hampele, IC ;
DArcy, A ;
Dale, GE ;
Kostrewa, D ;
Nielsen, J ;
Oefner, C ;
Page, MGP ;
Schonfeld, HJ ;
Stuber, D ;
Then, RL .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :21-30