Aggregatibacter actinomycetemcomitans

Aggregatibacter actinomycetemcomitans (previously Actinobacillus actinomycetemcomitans) is a Gram-negative, facultative anaerobe, nonmotile bacterium that is often found in association with localized aggressive periodontitis, a severe infection of the periodontium. It is also suspected to be involved in chronic periodontitis.[1] Less frequently, A. actinomycetemcomitans is associated with nonoral infections such as endocarditis. Its role in aggressive periodontitis was first discovered by Danish-born periodontist Jørgen Slots, a professor of dentistry and microbiology at the University of Southern California School of Dentistry.

Aggregatibacter actinomycetemcomitans
Scientific classification
Kingdom:
Bacteria
Phylum:
Proteobacteria
Class:
Gammaproteobacteria
Order:
Pasteurellales
Family:
Pasteurellaceae
Genus:
Aggregatibacter
Species:
actinomycetemcomitans
Binomial name
Aggregatibacter actinomycetemcomitans
(Klinger, 1912)

'Bacterium actinomycetem comitans' was first described by Klinger (1912) as coccobacillary bacteria isolated with Actinomyces from actinomycotic lesions in humans. It was reclassified as Actinobacillus actinomycetemcomitans by Topley & Wilson (1929) and as Haemophilus actinomycetemcomitans by Potts et al. (1985). The species has attracted attention because of its association with localized aggressive periodontitis.[2]

Nomenclature

Recent studies have shown a phylogenetic similarity of A. actinomycetemcomitans and Haemophilus aphrophilus, H. paraphrophilus, and H. segnis, suggesting the new genus Aggregatibacter for them.[2]

Importance

It is one of the bacteria that might be implicated in destructive periodontal disease. Although it has been found more frequently in localized aggressive periodontitis,[3] prevalence in any population is rather high. It has also been isolated from actinomycotic lesions (mixed infection with certain Actinomyces species, in particular A. israelii). It possesses certain virulence factors that enable it to invade tissues, such as the pore-forming toxin leukotoxin A. It has also been isolated from women with bacterial vaginosis and as an etiologic agent in endocarditis.[4] The pore-forming toxin LtxA of A. actinomycetemcomitans may be a trigger of the autoimmune disease rheumatoid arthritis due to its ability to stimulate protein citrullination, a post-translational protein modification targeted by autoantibodies in this disease.[5][6]

Virulence factors

A. actinomycetemcomitans serotypes
  • a strain, for example ATCC 29523, frequently in oral cavity, variable leukotoxin expression
  • b strain Y4, most frequently in localized aggressive periodontitis, high leukotoxin expression; of the b subset, clone Jp2 is particularly leukotoxic[7]
  • c strain ATCC 33384, low leukotoxin expression
  • serotypes d, e, f, g
  • within each serotype, leukotoxin expression can be highly variable between strains

Small RNA

In bacteria, small RNAs are involved in gene regulation. Jorth et al. identified 9 sRNA by Northern blotting from computer-predicted candidates in strain VT1169 and 202 sRNA by RNA seq in strain 624.[8][9] A systematic screen by RNA-seq and RT-PCR in HK1651 strain (a clinical isolate from an aggressive periodontitis patient), quantified 70 sRNAs and further identified 17 differentially expressed sRNAs during growth phases.[10] Target prediction indicated possibility of sRNA interaction with several virulence genes. [10] This study confirmed the presence of one of previously identified Fur regulated sRNAs JA04 identified in strain HK1651.

See also

References
  1. Henderson B, Ward JM, Ready D (October 2010). "Aggregatibacter (Actinobacillus) actinomycetemcomitans: a triple A* periodontopathogen?". Periodontology 2000. 54 (1): 78–105. doi:10.1111/j.1600-0757.2009.00331.x. PMID 20712635.
  2. Nørskov-Lauritsen N, Kilian M (September 2006). "Reclassification of Actinobacillus actinomycetemcomitans, Haemophilus aphrophilus, Haemophilus paraphrophilus and Haemophilus segnis as Aggregatibacter actinomycetemcomitans gen. nov., comb. nov., Aggregatibacter aphrophilus comb. nov. and Aggregatibacter segnis comb. nov., and emended description of Aggregatibacter aphrophilus to include V factor-dependent and V factor-independent isolates". International Journal of Systematic and Evolutionary Microbiology. 56 (Pt 9): 2135–46. doi:10.1099/ijs.0.64207-0. PMID 16957111.
  3. Slots J (January 1976). "The predominant cultivable organisms in juvenile periodontitis". Scandinavian Journal of Dental Research. 84 (1): 1–10. doi:10.1111/j.1600-0722.1976.tb00454.x. PMID 1061986.
  4. Africa CW, Nel J, Stemmet M (July 2014). "Anaerobes and bacterial vaginosis in pregnancy: virulence factors contributing to vaginal colonisation". International Journal of Environmental Research and Public Health. 11 (7): 6979–7000. doi:10.3390/ijerph110706979. PMC 4113856. PMID 25014248.
  5. Konig MF, Abusleme L, Reinholdt J, Palmer RJ, Teles RP, Sampson K, Rosen A, Nigrovic PA, Sokolove J, Giles JT, Moutsopoulos NM, Andrade F (December 2016). "Aggregatibacter actinomycetemcomitans-induced hypercitrullination links periodontal infection to autoimmunity in rheumatoid arthritis". Science Translational Medicine. 8 (369): 369ra176. doi:10.1126/scitranslmed.aaj1921. PMC 5384717. PMID 27974664.
  6. Abbasi J (March 2017). "To Prevent Rheumatoid Arthritis, Look Past the Joints to the Gums". JAMA. 317 (12): 1201–1202. doi:10.1001/jama.2017.0764. PMID 28273301.
  7. Haubek, Dorte (28 September 2010). "The highly leukotoxic JP2 clone of Aggregatibacter actinomycetemcomitans: evolutionary aspects, epidemiology and etiological role in aggressive periodontitis". APMIS. 118 (130): 1–53. doi:10.1111/j.1600-0463.2010.02665.x. PMID 21214629. S2CID 20882401.
  8. Jorth P, Whiteley M (December 2010). "Characterization of a novel riboswitch-regulated lysine transporter in Aggregatibacter actinomycetemcomitans". Journal of Bacteriology. 192 (23): 6240–50. doi:10.1128/JB.00935-10. PMC 2981213. PMID 20889741.
  9. Jorth P, Trivedi U, Rumbaugh K, Whiteley M (November 2013). "Probing bacterial metabolism during infection using high-resolution transcriptomics". Journal of Bacteriology. 195 (22): 4991–8. doi:10.1128/JB.00875-13. PMC 3811578. PMID 23974023.
  10. Oogai Y, Gotoh Y, Ogura Y, Kawada-Matsuo M, Hayashi T, Komatsuzawa H (December 2017). "Small RNA repertoires and their intraspecies variation in Aggregatibacter actinomycetemcomitans". DNA Research. 25 (2): 207–215. doi:10.1093/dnares/dsx050. PMC 5909427. PMID 29211829.
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