Fusobacterium
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Fusobacterium is a genus of obligate anaerobic, Gram-negative,<ref name=":5" /> non-sporeforming bacteria<ref>Template:Cite journal</ref> belonging to Gracilicutes. Individual cells are slender, rod-shaped bacilli with pointed ends.<ref>Template:Cite book</ref><ref>Taber's Cyclopedic Medical Dictionary, 22nd Edition, Template:ISBN, (2009)n p.983</ref> Fusobacterium was discovered in 1900 by Courmont and Cade and is common in the flora of humans.<ref name=":6">Template:Cite journal</ref><ref name=":8">Template:Cite journal</ref>
Strains of Fusobacterium can cause several human diseases and infections, including periodontal diseases, Lemierre's syndrome,<ref name=":1">Template:Cite journal</ref> oral, head, and neck infections, as well as colorectal cancer and topical skin ulcers.<ref name=":2">Template:Cite journal</ref>
It has been tiedTemplate:Clarify to HIV infection and suboptimal immune recovery.<ref name=":3">Template:Cite journal</ref> Detection of Fusobacterium is typically through surgical retrieval of tissue, fecal tests, or blood tests in patients showing symptoms.<ref name=":5">Template:Cite journal</ref> Early detection is preferred and helps to prevent further disease progression.<ref name=":6"/>
Although older sources state that Fusobacterium is part of the normal flora of the human oropharynx, the current consensus is that Fusobacterium should always be treated as a pathogen.<ref name="ludlam2004">Template:Cite journal</ref> There are thirteen described Fusobacterium strains; the predominant one affecting humans is F. nucleatum,<ref name=":0">Template:Cite journal</ref> followed by F. necrophorum, which also affects animals, mainly cattle.<ref name=":4">Template:Cite journal</ref>
BackgroundEdit
HistoryEdit
Although the genus was not discovered until 1900 by Courmont and Cade,<ref name=":6"/> the first documented Fusobacterium infection was reported in 1898 by Veillon and Zuber, who described a case of systemic infection in a young child.<ref>Template:Cite journal</ref> The genus was proposed by Knorr in 1923.<ref>Template:Cite journal</ref> Fusobacterium has been classically considered a normal part of the human oral, gastrointestinal, and female genital flora, which is why infections are not commonly seen.<ref name=":8" />
Clinical relevanceEdit
Fusobacterium is often associated with ulcerative colitis.<ref>Template:Cite journal</ref> Research of colon cancer has also shown an overrepresentation of Fusobacterium, both in feces of patients<ref name=Ahn2013>Template:Cite journal</ref> and tumor tissue itself.<ref name="TIME-Park2011">Template:Cite news</ref> Fusobacterium has also been seen increased in individuals infected with HIV as well as in individuals with suboptimal immune recovery as compared to patients who were not infected and had optimal responses.<ref name=":3" />
Prevalent pathogenic speciesEdit
F. nucleatum is found in humans more so than any other species of Fusobacterium.<ref name=":0" /> It is commonly found in the oral cavity as well as in the intestinal tract.<ref name=":2" /> Some of its pathogenic ties include its extraction from amniotic fluid sourced from spontaneous premature labor without reason/a given source.<ref name=":0" /> A few additional sources of its pathogenic nature include its association with oral inflammation diseases, cancers such as pancreatic, oral, and colorectal, as well as infections of the head and neck. This association is due to the high increase in the prevalence of F. nucleatum in those infected areas. F. nucleatum can worsen or initiate colorectal cancer by stimulating other bacteria such as Streptococcus, Campylobacter spp. and Leptotrichia as well as cancerous gene expression from Beta-catenin signaling. F. nucleatum can be detected in tissues, genomic DNA, and feces using methods such as (FQ, q, and dd) polymerase chain reaction and fluorescence in situ hybridization. However, these are limited because tissues can only be tested after surgery and fecal matter can return false positive results.<ref name=":2" />
F. necrophorum has been found as a common pathogen in the diagnostic of peritonsillar abscess and is more prevalent than other bacteria regarding this infection. It is also the most frequent leading cause associated with Lemierre Syndrome and is not proven to be a normal part of the human oral bacterium population.<ref name=":1" /> F. necrophorum commonly infects animals, causing liver abscesses and necrodic diseases, and can combine with other pathogenic bacteria to cause various infections such as foot rot<ref name=":4" /> and uterine infections.<ref>Template:Cite journal</ref>
Sources of other species of FusobacteriumEdit
Source:<ref name=":0" />
- F. ulcerans is very similar to F. varium and is commonly extracted from tropical ulcers.
- F. necrogenes is also closely related to F. ulcerans and F. varium and has been found in chickens and ducks.
- F. perfoetans is sourced from fecal matter. (F. perfoetans and F. necrogenes have not been sourced from any infections in humans or animals)
- F. gonidiaformans is typically found in the intestines of humans and is not found orally like the other Fusobacterium.
- F. russi is a common bacteria in canine and feline oral cavities and can lead to the infection of puncture wounds if transferred to humans from bites.
- F. simae which can be sourced from monkeys.
Symptoms and treatmentEdit
Fusobacterium infections often cause clinical symptoms such as a fever, inflammation, and a diseased appearance. Further diagnosis can confirm suspicions of Fusobacterium infection through blood testing or culturing the tissue. Upon diagnosing the infection, action to treat it involves the application of antibiotics over a 2-week period which could be in the form of penicillin or other variants as well as using anaerobic antibiotics like clindamycin and metronidazole which work when the Fusobacterium can break down the Beta-lactams. Leaving Fusobacterium untreated could lead to more severe developments of the infection and early testing is recommended.<ref name=":5" /> By testing early, fatal diseases such as Lemierre syndrome can be avoided. However, this requires the family physician to be conscious of the danger as infections such as Lemierre syndrome affects younger populations and especially those of male gender.<ref name=":6" /> The bacterium is a big anchor for biofilms.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> It is usually susceptible to clindamycin,<ref name="Davisclind">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> while approximately 20% of the clinical strains are resistant to penicillin.<ref>Template:Cite journal</ref> In contrast to Bacteroides spp., Fusobacterium has a potent lipopolysaccharide.
TaxonomyEdit
Current speciesEdit
Fusobacterium is divided into 13 different species, two of which each have their own set of subspecies (F. nucleatum and F. necrophorum).<ref name=":0" />
Reclassified speciesEdit
Other previously declared species of Fusobacterium such as F. symbiosum, F. praecutum, F. plauti, F. alocis, F. sulci, and F. prausnitzii have since been reclassified due to containing different characteristics from the other Fusobacterium members. F. alocis has been reclassified into Filifactor alocis while F. sulci has been reclassified as Eubacterium sulci. F. prausnitzii is a part of the Clostridium leptum subgroup under Eubacterium-like organisms.<ref name=":0" /> A few strains F. prausnitzii, a gut commensal associated with healthy patients, was completely reclassified as Faecalibacterium (Clostridiales:Ruminococcaceae) in 2002.
Phylogenic treeEdit
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See alsoEdit
ReferencesEdit
External linksEdit
- Anaerobic Gram-Negative Bacilli chapter in Baron's Medical Microbiology (online at the NCBI bookshelf).
- Fusobacterium From MicrobeWiki, the student-edited microbiology resource
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