Arcobacter

Arcobacter species have been discovered as both animal and human pathogens within the past decade, due to improvements in isolation techniques.[6] Up to now, little is known about the mechanisms of pathogenicity or potential virulence factors of Arcobacter spp.[9] Since no routine diagnostic of these bacteria has been performed, the global prevalence of Arcobacter infection is rather underestimated and the exact routes of transmission are unknown.[10] Some evidence indicates livestock animals may be a significant reservoir of Arcobacter, and over the last few years, the presence of these organisms in raw meat products, as well as in surface and ground water, has received increasing attention.[9] In humans, A. butzleri, and less commonly, A. cryaerophilus, have been linked to enteritis and occasionally bacteremia.[6] Symptoms of A. butzleri infections include diarrhea associated with abdominal pain, nausea, and vomiting or fever.[6] Studies of patients infected with A. butzleri have demonstrated that without treatment, symptoms endured for a very variable amount of time, from two days to several weeks.[7] When antimicrobial therapies were administered, the infection was eradicated within a few days, and all strains in the study were found to be susceptible to the antibiotics given.[7] A third species, A. skirrowii, has also recently been isolated from a patient with chronic diarrhea.[6] Although the microbiological and clinical features of Arcobacter are not yet well defined, initial studies of A. butzleri suggest that these bacteria display similar microbiological and clinical features as C. jejuni, but are more associated with a persistent, watery diarrhea than with the bloody diarrhea associated with C. jejuni.[6] Recent studies suggest that A. butzleri induces epithelial barrier dysfunction by changes in tight junction proteins and induction of epithelial apoptosis.[10] Based on this model, the virulence of A. butzleri seems to have two phases. An initial effect on tight junctions was observed first, followed by a late effect on cytotoxicity because of necrosis and induction of apoptosis.[10]

A. nitrofigilis is a nitrogen-fixing bacterium isolated from the roots of the salt marsh plant Spartina alterniflora.[5] A. sulfidicus is an obligate microaerophile that oxidizes sulfides and is an autotrophic producer of filamentous sulfur.[5] Large populations of this bacterium produce mats of this solid, white sulfur filament.[11] These mats are useful in anchoring the bacteria to rocky surfaces in the face of flowing subsurface hydrothermal fluids, as well as providing important carpeting around hydrothermal vents that attracts other animals to that site and encourages them to settle and grow.[11] One interesting potential novel Arcobacter species, designated LA31BT, was isolated from water collected from a hypersaline lagoon.[4] Preliminary characterization based on 16S rRNA gene sequence analysis showed that LA31BT shared 94% identity with A. nitrofigilis, the type species of the genus, and taxonomic studies confirmed the phylogenetic affiliation of strain LA31BT to the genus Arcobacter.[4] Other analytical methods, however, showed that LA31BT was distinct from all recognized Arcobacter species. Most notably and of interest, LA31BT was found to be an obligate halophile, a trait not found among recognized Arcobacter species.[4]

Another unusual Arcobacter species, designated strain CAB, was isolated from marine sediment and found to have the capacity to grow via perchlorate reduction, the only member of the Epsilonproteobacteria in pure culture to possess this rare metabolism.[12] Unlike most Arcobacter species, CAB was found to degrade carbohydrates, including fructose and catechol, and its cells often lacked the distinctive curvature typical of the genus Arcobacter.[12]