%0 Journal Article %1 yakubu_molecular_1999 %A Yakubu, D E %A Abadi, F J %A Pennington, T H %D 1999 %J Journal of Medical Microbiology %K Bacterial Humans, Infections, Meningococcal Neisseria Techniques, Typing meningitidis %N 12 %P 1055--1064 %T Molecular typing methods for Neisseria meningitidis %U http://www.ncbi.nlm.nih.gov/pubmed/10591158 %V 48 %X Neisseria meningitidis is an important pathogen because it causes life-threatening infections. The rapid course of meningococcal disease and the capacity of some serogroups to cause large-scale epidemics necessitates the use of sensitive, reliable and rapid typing methods to characterise strains. Molecular typing techniques for N. meningitidis are used for epidemiological purposes to investigate outbreaks and the spread of organisms and to examine the population genetic structure of the organism to understand better its variation and evolution. Many investigators have employed molecular typing methods and shown that meningococcal disease is associated with a variety of different epidemiological patterns. The choice of a typing method is dependent upon the epidemiological questions to be answered and on the population genetics of the organism under investigation. With highly clonal populations comprising independent non-recombining lineages such as serogroup A meningococci, ribotyping, multilocus enzyme electrophoresis (MLEE), pulsed-field gel electrophoresis (PFGE), multilocus sequence typing (MLST), PCR with arbitrary primers (RAPD) or with other gene-based primers each provides a constant measure of the relationship between strains. A more restricted portfolio of molecular methods - PFGE, MLEE and MLST - is appropriate for the investigation of less clonal serogroup B and C meningococci from localised outbreaks. If a thorough evaluation of the overall population is sought to determine the relationship between new isolates and members of hyper-endemic clonal complexes then quantitative methods such as MLEE and MLST are necessary. Several PCR-based methods are used for the detection and typing of meningococcal strains, many requiring rigorous standardisation before they can be considered suitable for rapid and reliable differentiation between clones. This review examines strain characterisation by molecular techniques and non-culture-based subtyping of meningococci in clinical specimens. It assesses the importance of these techniques and examines the epidemiological questions that they answer and also their limitations.

@article{yakubu_molecular_1999, abstract = {Neisseria meningitidis is an important pathogen because it causes life-threatening infections. The rapid course of meningococcal disease and the capacity of some serogroups to cause large-scale epidemics necessitates the use of sensitive, reliable and rapid typing methods to characterise strains. Molecular typing techniques for N. meningitidis are used for epidemiological purposes to investigate outbreaks and the spread of organisms and to examine the population genetic structure of the organism to understand better its variation and evolution. Many investigators have employed molecular typing methods and shown that meningococcal disease is associated with a variety of different epidemiological patterns. The choice of a typing method is dependent upon the epidemiological questions to be answered and on the population genetics of the organism under investigation. With highly clonal populations comprising independent non-recombining lineages such as serogroup A meningococci, ribotyping, multilocus enzyme electrophoresis {(MLEE),} pulsed-field gel electrophoresis {(PFGE),} multilocus sequence typing {(MLST),} {PCR} with arbitrary primers {(RAPD)} or with other gene-based primers each provides a constant measure of the relationship between strains. A more restricted portfolio of molecular methods - {PFGE,} {MLEE} and {MLST} - is appropriate for the investigation of less clonal serogroup B and C meningococci from localised outbreaks. If a thorough evaluation of the overall population is sought to determine the relationship between new isolates and members of hyper-endemic clonal complexes then quantitative methods such as {MLEE} and {MLST} are necessary. Several {PCR-based} methods are used for the detection and typing of meningococcal strains, many requiring rigorous standardisation before they can be considered suitable for rapid and reliable differentiation between clones. This review examines strain characterisation by molecular techniques and non-culture-based subtyping of meningococci in clinical specimens. It assesses the importance of these techniques and examines the epidemiological questions that they answer and also their limitations.}, added-at = {2011-03-11T10:05:34.000+0100}, author = {Yakubu, D E and Abadi, F J and Pennington, T H}, biburl = {https://www.bibsonomy.org/bibtex/21610e347dd0366e34357b40a59c183f5/jelias}, interhash = {38f7b83e79dbbcc2e67bb90ec46ca71a}, intrahash = {1610e347dd0366e34357b40a59c183f5}, issn = {0022-2615}, journal = {Journal of Medical Microbiology}, keywords = {Bacterial Humans, Infections, Meningococcal Neisseria Techniques, Typing meningitidis}, month = dec, note = {{PMID:} 10591158}, number = 12, pages = {1055--1064}, timestamp = {2011-03-11T10:06:39.000+0100}, title = {Molecular typing methods for Neisseria meningitidis}, url = {http://www.ncbi.nlm.nih.gov/pubmed/10591158}, volume = 48, year = 1999 }