A Microbial Biorealm page on the genus Neisseria elongata
Higher order taxa
root; cellular organisms; Bacteria; Proteobacteria; Betaproteobacteria; Neisseriales; Neisseriaceae; Neisseria
N. elongata subsp. elongata, N. elongata subsp. glycolytica, N. elongata subsp. nitroreducens,
Description and significance
Neisseria elongata, formerly known as Centers for Disease Control (CDC) group M6, was described by Bovre and Holten in 1970 as a gram-negative, rod-shaped bacterium of the family Neisseriaceae, where it is found in the oral bacterial flora of the human pharynx and throat or in the blood of those infected (2). N. elongata consists of three subspecies, N. elongata subsp. elongata, N. elongata subsp. glycolytica, and N. elongata subsp. nitroreducens, in which are separated based on their biochemical differences (4). Although these subspecies of N. elongata were previously believed to be nonpathogenic to humans, recent case studies from patients suffering from endocarditis, have indicated that all three N. elongata subspecies are associated with human disease, particularly endocarditis and osteomyelitis (3).
Although the N. elongata genome has not yet been sequenced, the importance of sequencing its genome will provide information on the three N. elongata subspecies that could possibly assist in distinguishing their pathogenic roles in endocarditis and osteomyelitis. Before the pathogenic roles of all three N. elongata subspecies were discovered, where N. elongata subsp. nitroreducens was the first subspecies to be discovered as pathogenic, N. elongata subsp. elongata and N. elongata subsp. glycolytica were considered just to be transient colonizers of the human upper respiratory tract and urogentical tract (4). Thus, the sequencing of their genomes could possibly provide further insight into the differences and similarities involved in the factors influencing the metabolism and virulent features of the three N. elongata subspecies.
Describe the size and content of the genome. How many chromosomes? Circular or linear? Other interesting features? What is known about its sequence? Does it have any plasmids? Are they important to the organism's lifestyle?
Cell structure and metabolism
N. elongata is a nonmotile, aerobic, catalase-negative, asaccharolytic, oxidase-positive, urea-negative, gram-negative coccobacilli with an optimal growth temperature at 35 degrees Celsius (5). Before the isolation and characterization of Neisseria bacilliformis, the second and more recent bacilliary Neisseria species that was isolated from human infections, N. elongata was the only bacillary Neisseria species derived from humans. The rod-like shape of N. elongata makes it unique from the other Neisseria species, which are either cocci or diplococci (6). Thus, it is critical to avoid classifying N. elongata strains based on the diplococcal morphology typically associated with the majority of the Neisseria species.
The classification of N. elongata into three different subspecies, N. elongata subsp. elongata, N. elongata subsp. glycolytica, and N. elongata subsp. nitroreducens, are based on the biochemical differences between each subspecies. N. elongata subsp. nitroreducens are different from N. elongata subsp. elongata and N. elongata subsp. glycolytica in its ability to reduce nitrate (7). N. elongata subsp. glycolytica differs from the other subspecies based on its feature of testing positive for catalase, an enzyme involved in the decomposition of toxic hydrogen peroxide to water and oxygen (5). N. elongata subsp. elongata differs from the other two subspecies due to its inability to produce acid from D-glucose (4).
Being strictly aerobic, N. elongata requires oxygen to oxidize substrates in order to obtain energy. The ability of N. elongata subsp. glycolytica and N. elongata subsp. nitroreducens to produce acid from D-glucose is another method of energy acquisition, as an accumulation of small amounts of acidic intermediates are formed when glucose is broken down (4).
Ecology and Pathology
N. elongata is found in the bacterial flora of the human pharynx, respiratory secretions, and blood (3, 8). Cases of N. elongata infections have been reported in the USA, Europe, Canada, Australia, and in the UK (3); the first diagnosis of N. elongata subsp. nitroreducens associated endocarditis was reported in New Zealand in 1978 (7). There has been no extensive research performed on the interactions of N. elongata with other organisms that live in its environment.
Through reports of case studies on patients from whom the N. elongata subspecies were isolated and characterized, it is indicated that N. elongata are capable of producing systemic diseases, such as endocarditis, septicemia, and osteomyelitis (8). N. elongata has only been found in humans, where risk factors for developing N. elongata infections are believed to include dental manipulations and/or a previous history of valvular heart disease, such as endocarditis, valve damage, or rheumatic fever (5). Studies have shown that N. elgonata is fully sensitive to the antibiotics amoxicillin, gentamicin, cefuroxime, and ciprofloxacin, yet having reduced sensitivity to penicillin and trimethoprim. However, endocarditis caused by N. elongata infections typically require early surgical invention as treatment with antibiotics alone may not be sufficient (3).
Although N. elongata infection cases were documented beginning in 1978 (7), the cases of N. elongata infections are uncommon in comparison to other species in the same Neisseria genus, particularly N. gonorrhoeae and N. menigitidis, which have caused between an estimated 500,000 to 1 million cases of septicemia and meningitis each year (9). Thus, there is a lack of extensive research that has been performed on the actual methods in which the bacteria, N. elongata, causes disease in the human host, possibly also due to the fact that its genome has not yet being sequenced.
Enter summaries of the most recent research here--at least three required
(1) NCBI: Neisseria elongata, Accessed August 26, 2007, <http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=495&lvl=3&lin=f&keep=1&srchmode=1&unlock>
(2) Bovre K, Holten F. "Neisseria elongata sp. nov., a rod-shaped member of the genus Neisseria. Re-evaluation of cell shape as a criterion in classification," "J Gen Microbiol." 1970. Volume 60. p. 67-75.
(3) Haddow L. J., Mulgrew C., Ansari A., Miell J., Jackson G., Malnick H. and Gogal Rav G. “Neisseria elongata endocarditis: case report and literature review,” “European Society of Clinical Microbiology and Infectious Diseases.” 2003. Volume 9. p. 426-430.
(4) Anderson B. M., Weyant R. S., Steigerwalt A. G., Moss C. W., Hollis D. G., Weaver R. E., Ashford D., and Brenner D. J. “Characterization of Neisseria elongata subsp. glycolytica Isolates Obtained from Human Wound Specimens and Blood Cultures,” “Journal of Clinical Microbiology.” 1994. Volume 33. p. 76-78.
(5) Apisarnthanarak A., Dunagan C., and Dunne M. Jr. “Neisseria elongata subsp. elongata, as a cause of human endocarditis,” “Diagnostic Microbiology and Infectious Disease.” 2001. Volume 39. p. 265-266.
(6) Han X. Y., Hong T., and Falsen E. “Neisseria bacilliformis sp. nov. Isolated from Human Infections,” “Journal of Clinical Microbiology.” 2005. Volume 44. p. 474-479.
(7) Grant P. E., Brenner D. J., Steigerwalt A. G., Hollis D. G., and Weaver R. E. “N. elongata subsp. nitroreducens subsp. nov., Formerly CDC Group M-6, a Gram-Negative Bacterium Associated with Endocarditis,” “Journal of Clinical Microbiology.” 1990. p. 2591-2596.
(8) Wong J. D., and Janda M. “Association of an Important Neisseria Species, Neisseria elongata subsp. nitroreducens, with Bacteremia, Endocarditis, and Osteomyelitis,” “Journal of Clinical Microbiology.” 1991. Volume 30. p. 719-720.
(9)Dietrich G., Kurz S., Hubner C., Aepinus C., Theiss S., Guckenberger M., Panzner R., Weber J., and Frosch M. "Transcriptome analysis of Neisseria meningitidis during infection," "Journal of Bacteriology." 2003. Volume 185. p. 155-164.
Edited by Cindy Wu, student of Rachel Larsen