Anaerococcus

Anaerococcus is a genus of bacteria. Its type species is Anaerococcus prevotii.[1] These bacteria are Gram-positive and strictly anaerobic.[2][3][4] The genus Anaerococcus was proposed in 2001.[2][4] Its genome was sequenced in August 2009. The genus Anaerococcus is one of six genera classified within the group GPAC (Gram-Positive Anaerobic Cocci).[5] These six genera (Peptostreptococcus, Peptoniphilus, Parvimonas, Finegoldia, Anaerococcus and Murdochiella) are found in the human body as part of the commensal human microbiota.[6][7][5]

Anaerococcus
Scientific classification
Domain:
Bacteria
Phylum:
Firmicutes
Class:
Clostridia
Order:
Clostridiales
Genus:
Anaerococcus

It can cause infection and is a normal part of the human microbiome.[8] Most of the species in this genus can be found as part of the normal flora of the skin, human vagina, nasal cavity, oral cavity and feces.[2] It is a pathogen of humans found in ovarian abscesses, chronic wounds and vaginal discharge.[9] Moreover, some of the species can be isolated from foot ulcers and knee arthirtis.[2] It can be present in urinary tract infections, chronic ulcers, pleural empyema, blood infections, and soft tissue infections. It is involved in polymicrobial infections.[10] Farther more, strains of Anaerococcus were found in the armpit microbiota suggesting some species in this genus could play a role in axillary odor.[10][11]

Physiology

The genus Anaerococcus are non motile bacteria who can not form spores and.[4][12][2] Depending of the species the arrangement can be different. The most common arrangements within this genus are pairs, tetrads, short chains and irregular formations.[10][4] Their cells size can differ from 0.6μm to 0.9μm.[10] However, when they are grown using enrinched blood agar their size can go from 0.5μm to 2μm.[10] In this genus, there a more than one major cellular fatty acids: C18:1, C16:1, C18 and C16.[12] Most species in this genus are indole-negative and coaguase-negative.[10] In general, the species of Anaerococcus presents susceptibility to penicillins but are resistant to tetracycline, erythromycin and clindamycin.[9]

Metabolism

The genus Anaerococcus are classified as saccharolytic bacteria.[2][13] Its species can be arranged from weakly saccharolytic (ex. A. prevotii, A. lactolyticus) to strongly saccharolytic (ex. A. hydrogenalis).[13] This genus can ferment carbohydrates weakly.[6] The major sources of energy use in the metabolism of Anaerococcus are peptones and aminoacids.[4][10] The three major sugars fermented within this genus are glucose, mannose, fructose and sucrose.[12][4] After fermenting the sugars, Anaerococcus produce weak acids as their metabolic end product.[13] Within these metabolic end products, this genus ca produce butyric acid, lactic acid, and some propionic and succinic acid.[12] Nonetheless, the major metabolite produced by Anaerococcus is butyrate.[13][10][2]

Species

Until recently, the genus Anaerococcus have 14 known species.[14][9] Six of the species were initially classified in the genus Peptostreptococcus but then based on their characteristics were re-classified in the new genus Anaerococcus: A. hydrogenalis, A. lactolyticus, A. octavius, A. prevotii, A. tetradius, and A. vaginalis.[5][2] Throughout the years, the specie who has been more commolny found on the body within this genus is A. prevotii.[9]

Anaerococcus hydrogenalis

A. hydrogenalis it is present in vaginal discharges and oarian abscesses.[4] Presence of Anaerococcus hydrogenalis in the gut metabolism and their coline consumption has been associated to cardiovascular diseases.[15] Contrary to most of the species in this genus, Anaerococcus hydrogenalis is indole-positive.[4] Also, some strains in this specie can produce urease.[4]

Anaerococcus lactolyticus

Anaerococcus lactolyticus[10] is one of two species of the genus Anaerococcus who have been found from diabetic foot.[9] Moreover, A. lactolyticus can be extracted from pressure ulcers.[9]

Anaerococcus octavius

Contrary to most of the species in the genus, Anaerococcus octavius was not related to human infections.[9] Nevertheless, recently a new case revealed A. octavius can cause bacteremia.[9] Even though is uncommon, Anaerococcus octavius can be the cause for human infections.[9] Other studies has found A. octavius as part of the nasal cavity, skin and vagina normal flora.[9][4] This bacteria can ferment ribose, glucose, and mannose.[4]

Anaerococcus prevotii

A. prevotii is normally found in vaginal discharges, human plasma and some types of abscesses as ovarian, peritoneal sacral and/or lung abscesses.[9][6] Even more, Anaerococcus prevotii is part of the normal flora in the skin, oral cavity and the gut.[6] Studies has shown Anaerococcus prevotii presents resistance to Ceftazidime, Clindamycin, Levofloxacin.[9] Unlike the other species, A. prevotii can not ferment glucose.[16]

Anaerococcus tetradius

A. tetradius was first isolated from vaginal discharges and ovarian abscesses.[4] This bacteria can ferment glucose and mannose.[4]

Anaerococcus vaginalis

A. vaginalis was first recovered from vaginal discharges and ovarian abscesses although this bacteria can also be found in pressure ulcers and diabetic foot.[4][9] Some strains from this specie can be indole-positive.[4]

Anaerococcus murdochii

A. murdochii presents resistance against antiobiotics clindamycin and kanamycin.[9] Also, studies have discovered this species have intermedite resistance to pencillins.[9]

Anaerococcus degenerii

A. degenerii

Anaerococcus provencensis

A. provencensis was isolated from a cervical abscess.[17] This specie can ferment lactose, unlike A. tetradius, A. prevotii, and A. octavius.[17] The first analysis made on Anaerococcus provencensis showed it is susceptible to penicillin G, imipenem, amoxillin, metronidazole, cefotetan and vancomycin.[17]

Anaerococcus senegalensis

A. senegalensis is one of the few species in Anerococcus whose genome has been sequenced.[2] The genome has a size of 1,790,835 bp.[2] Analsis made did not show presence of a plasmid.[2] Initially, Anaerococcus senegalensis was found in the fecal flora of a healthy person.[2]

Anaerococcus rubiinfantis

A. rubiinfantis was discovered from a stool sample taken from an infant with severe acute malnutrition in Senegal.[18] Based on a genomic analysis, Anaerococcus rubiinfantis has high antibiotic susceptibility.[18] For that reason this bacteria can be treated with common oral antibiotics.[18] A. rubiinfantis have catalase activity, which is not common from an anaerobic bacteria.[18]

Anaerococcus marasmi

A. marasmi was first found in 2016 from a stool sample on a child with marasmus.[14] Just like A. rubiinfantis, Anaerococcus marasmi is catalse positive.[14] A. marasmi can grow in a range of pH between 6.5 to 8.[14] Moreover, A. marasmi has a high sequence similarity (97.6%) with A. prevotii based on their 16S rRNA.[14]

Anaerococcus urinomassiliensis

A. urinomassiliensis was isolated from an urine sample of a male adolescent with membranoproliferative glomerulonephritis and autoinmune hepatitis.[19] It took 10 days of anaerobic incubation to observe growth from this bacteria.[19] Anaerococcus urinomassiliensis does not have either oxidase or catalse activity.[19]

Anaerococcus nagyae

A. nagyae was first found in a blood culture from a patient with ischemia and influenza.[5] The cells of Anaerococcus nagyae are arranged in pairs.[5] Although it can weakly ferment mannose, studies has shown this anaerobic bacteria can not ferment glucose and raffinose.[5] A. nagyae is resistant to colistin, but it is susceptible to vancomycin and kanamycin.[5]

References
  1. Parte, A.C. "Anaerococcus". Retrieved 27 March 2017.
  2. Lagier JC, El Karkouri K, Nguyen TT, Armougom F, Raoult D, Fournier PE (March 2012). "Non-contiguous finished genome sequence and description of Anaerococcus senegalensis sp. nov". Standards in Genomic Sciences. 6 (1): 116–25. doi:10.4056/sigs.2415480. PMC 3359877. PMID 22675604.
  3. Versalovic J, Carroll KC, Funke G, Jorgensen JH, Landry ML, Warnock DW, eds. (2011-01-01). "Peptostreptococcus, Finegoldia, Anaerococcus, Peptoniphilus, Veillonella, and Other Anaerobic Cocci". Manual of Clinical Microbiology (10th ed.). American Society of Microbiology. pp. 803–816. doi:10.1128/9781555816728.ch48. ISBN 978-1-55581-463-2. Retrieved 2020-08-02.
  4. Ezaki T, Kawamura Y, Li N, Li ZY, Zhao L, Shu S (July 2001). "Proposal of the genera Anaerococcus gen. nov., Peptoniphilus gen. nov. and Gallicola gen. nov. for members of the genus Peptostreptococcus". International Journal of Systematic and Evolutionary Microbiology. 51 (Pt 4): 1521–1528. doi:10.1099/00207713-51-4-1521. PMID 11491354.
  5. Veloo AC, de Vries ED, Jean-Pierre H, van Winkelhoff AJ (April 2016). "Anaerococcus nagyae sp. nov., isolated from human clinical specimens". Anaerobe. 38: 111–115. doi:10.1016/j.anaerobe.2015.11.009. PMID 26639871.
  6. Labutti K, Pukall R, Steenblock K, Glavina Del Rio T, Tice H, Copeland A, et al. (September 2009). "Complete genome sequence of Anaerococcus prevotii type strain (PC1)". Standards in Genomic Sciences. 1 (2): 159–65. doi:10.4056/sigs.24194. PMC 3035230. PMID 21304652.
  7. Veloo AC, Elgersma PE, van Winkelhoff AJ (June 2015). "Anaerococcus degenerii sp. nov., isolated from human clinical specimens". Anaerobe. 33: 71–5. doi:10.1016/j.anaerobe.2015.02.002. PMID 25680238.
  8. "BacMap". Retrieved 27 March 2017.
  9. Cobo F, Navarro-Marí JM (February 2020). "First description of Anaerococcus octavius as cause of bacteremia". Anaerobe. 61: 102130. doi:10.1016/j.anaerobe.2019.102130. PMID 31765706.
  10. Murphy EC, Frick IM (July 2013). "Gram-positive anaerobic cocci--commensals and opportunistic pathogens". FEMS Microbiology Reviews. 37 (4): 520–53. doi:10.1111/1574-6976.12005. PMID 23030831.
  11. Fujii, Takayoshi; Shinozaki, Junko; Kajiura, Takayuki; Iwasaki, Keiji; Fudou, Ryosuke (July 2014). "A newly discovered Anaerococcus strain responsible for axillary odor and a new axillary odor inhibitor, pentagalloyl glucose". FEMS Microbiology Ecology. 89 (1): 198–207. doi:10.1111/1574-6941.12347. PMID 24784923.
  12. Ezaki, Takayuki; Ohkusu, Kiyofumi (2015), "Anaerococcus", Bergey's Manual of Systematics of Archaea and Bacteria, American Cancer Society, pp. 1–5, doi:10.1002/9781118960608.gbm00712, ISBN 978-1-118-96060-8
  13. Ezaki, Takayuki; Li, Na; Kawamura, Yoshiaki (2006), Dworkin, Martin; Falkow, Stanley; Rosenberg, Eugene; Schleifer, Karl-Heinz (eds.), "The Anaerobic Gram-Positive Cocci", The Prokaryotes: Volume 4: Bacteria: Firmicutes, Cyanobacteria, New York, NY: Springer US, pp. 795–808, doi:10.1007/0-387-30744-3_26, ISBN 978-0-387-30744-2
  14. Tall ML, Pham TP, Bellali S, Ngom II, Delerce J, Lo CI, et al. (May 2020). "marasmi sp. nov., a new bacterium isolated from human gut microbiota". New Microbes and New Infections. 35: 100655. doi:10.1016/j.nmni.2020.100655. PMC 7082211. PMID 32211195.
  15. Yadav M, Verma MK, Chauhan NS (March 2018). "A review of metabolic potential of human gut microbiome in human nutrition". Archives of Microbiology. 200 (2): 203–217. doi:10.1007/s00203-017-1459-x. PMID 29188341. S2CID 3464103.
  16. Song Y, Liu C, Finegold SM (June 2007). "Peptoniphilus gorbachii sp. nov., Peptoniphilus olsenii sp. nov., and Anaerococcus murdochii sp. nov. isolated from clinical specimens of human origin". Journal of Clinical Microbiology. 45 (6): 1746–52. doi:10.1128/JCM.00213-07. PMC 1933094. PMID 17428937.
  17. Pagnier I, Croce O, Robert C, Raoult D, La Scola B (June 2014). "Non-contiguous finished genome sequence and description of Anaerococcus provenciensis sp. nov". Standards in Genomic Sciences. 9 (3): 1198–210. doi:10.4056/sigs.5501035. PMC 4149013. PMID 25197492.
  18. Tidjani Alou M, Khelaifia S, Michelle C, Andrieu C, Armstrong N, Bittar F, et al. (August 2016). "Anaerococcus rubiinfantis sp. nov., isolated from the gut microbiota of a Senegalese infant with severe acute malnutrition". Anaerobe. 40: 85–94. doi:10.1016/j.anaerobe.2016.06.007. PMID 27328611.
  19. Morand A, Cornu F, Tsimaratos M, Lagier JC, Cadoret F, Fournier PE, Raoult D (September 2016). "Anaerococcus urinomassiliensis sp. nov., isolated from a urine sample of a 17-year-old boy affected by autoimmune hepatitis and membranoproliferative glomerulonephritis". New Microbes and New Infections. 13: 56–8. doi:10.1016/j.nmni.2016.06.001. PMC 4933030. PMID 27408746.


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