scholarly journals Resveratrol selectively inhibits Neisseria gonorrhoeae and Neisseria meningitidis

2001 ◽  
Vol 47 (2) ◽  
pp. 243-244 ◽  
Author(s):  
J. J. Docherty
2002 ◽  
Vol 46 (12) ◽  
pp. 3744-3749 ◽  
Author(s):  
Satoshi Ameyama ◽  
Shoichi Onodera ◽  
Masahiro Takahata ◽  
Shinzaburo Minami ◽  
Nobuko Maki ◽  
...  

ABSTRACT Neisseria gonorrhoeae strains with reduced susceptibility to cefixime (MICs, 0.25 to 0.5 μg/ml) were isolated from male urethritis patients in Tokyo, Japan, in 2000 and 2001. The resistance to cephems including cefixime and penicillin was transferred to a susceptible recipient, N. gonorrhoeae ATCC 19424, by transformation of the penicillin-binding protein 2 gene (penA) that had been amplified by PCR from a strain with reduced susceptibility to cefixime (MIC, 0.5 μg/ml). The sequences of penA in the strains with reduced susceptibilities to cefixime were different from those of other susceptible isolates and did not correspond to the reported N. gonorrhoeae penA gene sequences. Some regions in the transpeptidase-encoding domain in this penA gene were similar to those in the penA genes of Neisseria perflava (N. sicca), Neisseria cinerea, Neisseria flavescens, and Neisseria meningitidis. These results showed that a mosaic-like structure in the penA gene conferred reductions in the levels of susceptibility of N. gonorrhoeae to cephems and penicillin in a manner similar to that found for N. meningitidis and Streptococcus pneumoniae.


1979 ◽  
Vol 9 (5) ◽  
pp. 598-600
Author(s):  
P C Appelbaum ◽  
R B Lawrence

A radiometric procedure was compared with the Minitek and Cystine Trypticase Agar sugar degradation methods for identification of 113 Neisseria species (58 Neisseria meningitidis, 51 Neisseria gonorrhoeae, 2 Neisseria lactamica, 2 Neisseria sicca). Identification of meningococci and gonococci was confirmed by agglutination and fluorescent antibody techniques, respectively. The Minitek method identified 97% of meningococci, 92% of gonococci, and 100% of other Neisseria after 4 h of incubation. The radiometric (Bactec) procedure identified 100% of gonococci and 100% of miscellaneous Neisseria after 3 h, but problems were encountered with meningococci: 45% of the later strains yielded index values for fructose between 20 and 28 (recommended negative cut-off point, less than 20), with strongly positive (greater than 100) glucose and maltose and negative o-nitrophenyl-beta-D-galactopyranoside reactions in all 58 strains. The Cystine Trypticase Agar method identified 91% of meningococci, 90% of gonococci, and 100% of other Neisseria after 24 to 48 h. Prolongation of the Cystine Trypticase Agar incubation period led to abnormal lactose/sucrose reactions in some meningococci and gonococci. Radiometric and Minitek systems are more accurate and convenient than Cystine Trypticase Agar techniques, but, on the basis of these results, radiometric fructose sensitivity levels for meningococci need reevaluation.


1984 ◽  
Vol 11 (4) ◽  
pp. 296-300 ◽  
Author(s):  
JEAN-GUY BISAILLON ◽  
PIERRE TURGEON ◽  
DANIEL DUBREUIL ◽  
REJEAN BEAUDET ◽  
MICHEL SYLVESTRE ◽  
...  

Author(s):  
Kimberley V. Sukhum ◽  
Sophonie Jean ◽  
Meghan Wallace ◽  
Neil Anderson ◽  
Carey-Ann D. Burnham ◽  
...  

Neisseria meningitidis (Nm) and Neisseria gonorrhoeae (Ng) are pathogenic bacteria that can cause human infections. While Nm infections are associated with bacterial meningitis and bacteremia, a strain of Nm, isolated from the urogenital system, has recently been associated with urethritis. As this strain is becoming prominent as an emerging pathogen, it is essential to assess identification tools for Nm and Ng urogenital isolates. Consecutive Nm isolates recovered from urogenital cultures of symptomatic patients with presumptive diagnoses of gonorrhea and a random selection of Ng isolates recovered from the same population within the same time frame were characterized with routine identification systems, antimicrobial susceptibility testing, and whole genome sequencing. MALDI-ToF MS, multilocus sequence typing, 16S rRNA gene sequence, and average nucleotide identity methods accurately identified 95% (18/19) of Nm and Ng isolates. 30% (3/10) of Nm isolates were misidentified as Ng with Aptima Combo 2 CT/NG but no misidentifications were found with the Xpert CT/NG NAAT. Phylogenetic core genome and SNP-based grouping analyses showed that urogenital Nm isolates were highly related, and phylogenetically distinct from Ng and respiratory Nm isolates but similar to urogenital Nm isolates from patients with urethritis in the US. Urogenital Nm isolates were predominantly azithromycin resistant while Ng isolates were azithromycin susceptible. These data indicate that urogenital isolates of Nm can cause false-positive detections with Ng diagnostic assays. Misidentification of urogenital Nm isolates may confound public health-related activities for gonorrhea and future studies are needed to understand the impact on clinical outcome of Nm urogenital infection.


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