1995
DOI: 10.1128/jcm.33.4.1039-1041.1995
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Differentiation of Neisseria gonorrhoeae isolates requiring proline, citrulline, and uracil by plasmid content, serotyping, and pulsed-field gel electrophoresis

Abstract: A combination of DNA macrorestriction analysis using pulsed-field gel electrophoresis and a serotyping method using three panels of monoclonal antibody was used to discriminate 43 epidemiologically unrelated Neisseria gonorrhoeae isolates requiring proline, citrulline, and uracil (PCU ؊ ) into 35 groups. This indicates that PCU ؊ isolates of N. gonorrhoeae are not clonal.

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Cited by 24 publications
(10 citation statements)
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“…According to these results PFGE fingerprinting is a sharper and more discriminating epidemiologic tool than the routinely used serological typing. This is in full agreement with previous studies [82,83,87].…”
Section: Typing Methodssupporting
confidence: 94%
See 1 more Smart Citation
“…According to these results PFGE fingerprinting is a sharper and more discriminating epidemiologic tool than the routinely used serological typing. This is in full agreement with previous studies [82,83,87].…”
Section: Typing Methodssupporting
confidence: 94%
“…From each suspension 300 µL was used for preparation and digestion of the genomic DNA of the bacteria according to the manufacturer's protocol of GenePath Group 3 Reagent Kit (Bio-Rad Laboratories, Hercules, CA, USA). Two different restriction enzymes were separately used: SpeI recommended by Bio-Rad and used in previous studies [82][83][84][85][86] and BglII also used in previous studies [86,87].…”
Section: Genetic Characterisation By Pfgementioning
confidence: 99%
“…Chromosomal DNA was prepared by the procedure described by Van Looveren et al (27), except that no lysis step was performed. Four restriction enzymes used in other studies for the typing of gonococci, BglII, NheI, SpeI, and XbaI (13,14,19,22,32), were tested under various running conditions. All produced comparable results.…”
Section: Ardramentioning
confidence: 99%
“…Isoenzyme typing based on multilocus enzyme electrophoresis is widely applicable for epidemiological studies of diverse groups of pathogens, including N. gonorrhoeae (16,18,23). Genetic relatedness of gonococcal isolates has also been assessed by using DNA-based typing techniques, including restriction endonuclease analysis using frequently or rarely cut-ting enzymes (7,14,20,31,32), and random and repetitivemotif-based amplification of polymorphic DNA fragments (2,21). The discriminatory abilities of pulsed-field gel electrophoresis (PFGE) and random and repetitive-motif-based amplification of polymorphic DNA have been shown to be superior to that of traditional A/S typing (2,14,21,32).…”
mentioning
confidence: 99%
“…However, a short or long transmission chain has not been defined by the numbers of sexual partners. It has been shown that the majority of isolates of N. gonorrhoeae from sexual contacts have the same phenotype (3,11) and genotype, determined by a variety of genotypic methods (10,17,22,24,25). As N. gonorrhoeae is highly efficient at all points of its life cycle for recombination (2), persistence of a particular genotype over time should not in theory occur, particularly in genes where genetic variations accumulate very rapidly.…”
mentioning
confidence: 99%