Campylobacter upsaliensis
| Campylobacter upsaliensis | |
|---|---|
Scientific classification 
| |
| Domain: | Bacteria |
| Phylum: | Proteobacteria |
| Class: | Epsilonproteobacteria |
| Order: | Campylobacterales |
| Family: | Campylobacteraceae |
| Genus: | Campylobacter |
| Species: | C. upsaliensis
|
| Binomial name | |
| Campylobacter upsaliensis Sandstedt and 1991[1]
| |
Campylobacter upsaliensis is a gram negative bacteria in the Campylobacter genus.[2] C. upsaliensis is found worldwide, and is a common cause of campylobacteriosis in humans, as well as gastroenteritis in dogs.[3] Human infections are primarily associated with raw or undercooked meat and contaminated water sources, however there is some zoonotic risk associated with the spread from dogs.[4] C. upsaliensis primarily affects the gastrointestinal tract as it damages gastrointestinal epithelial cells.[5] There are many methods for detecting C.upsaliensis including PCR and ELISA, however there is no current gold standard in detection techniques.[4] Infection is typically self limiting, however there is antimicrobial therapy available.[6]
Cellular morphology and biochemistry[]
Campylobacter upsaliensis shares the characteristic appearance of other Campylobacter species: it is a curved to spiral, gram-negative rod that displays darting motility.[2][7] The bacterium either have one polar flagellum, or two flagella with one at either end, and can range from 0.2μm to 0.5μm in width and 0.5μm to 8μm in length. When grown on blood agarthe colonies appear smooth, well defined, and grey to translucent.[2] C. upsaliensis is catalase negative, distinguishing it from some other Campylobacter species which are catalase positive.[8] This species is also considered thermotolerant, having been shown to grow in culture at 42 °C, and microaerophilic, generally requiring an oxygen concentration around 5%.[2][9] In addition, C. upsaliensis is oxidase positive, like many other species within the genera.[2][8][10]
Epidemiology[]
Campylobacter upsaliensis is found worldwide and is among the predominant Campylobacter spp. associated with enteritis in companion animals.[11] Diarrhetic dogs are considered a possible source for human infections, though there may also be host-specific strains. Sources for companion animals include raw or undercooked meats, especially poultry.[12][13] Poor sanitary conditions in kennels and shelters where animals are in direct contact with feces have also been implicated.[14] Humans can become infected after contact with contaminated cat and dog feces, which accounts for a small percentage of human campylobacteriosis cases.[13] The majority of human cases are food-borne. Younger animals and children with underdeveloped immune systems are at greatest risk of infection.[14] C. upsaliensis infections are usually isolated events that don’t evolve into outbreaks, and the infection is generally self-limiting.[13]
Dogs may also be asymptomatically infected and act as carriers, so dog feces should always be handled carefully even if the animal isn’t diarrhetic. It is unknown how long infected animals shed C. upsaliensis in feces, but stressful events may increase shedding.[14] The proportion of animals carrying C. upsaliensis is 66% in cats 75% in dogs.[15]
Disease[]
Dogs[]
In dogs, Campylobacter upsaliensis can cause a mild to moderate form bacterial gastroenteritis.[4] It is also frequently associated with part of the normal microbiota in a large proportion of dogs.[16] In affected animals, symptoms include watery to mucoid diarrhea, abdominal cramping, lethargy and fever.[17] The infection is typically self limiting and doesn't require intervention.[17] Since C.upsaliensis is isolated from many healthy dogs, a positive identification of C. upsaliensisfrom a diarrhetic dog does not necessarily indicate causation.[18]
Humans[]
Campylobacter upsaliensis infections in humans can cause Campylobacteriosis, a more significant gastroenteritis.[3] C. upsaliensis is the second most common Campylobacter species isolated in humans with diarrhea (behind Campylobacter jejuni).[3] Clinical signs include fever, diarrhea (sometimes bloody), and stomach cramps.[19] It is typically a self limiting infection, however immunosuppressed individuals are more at risk for adverse events, such as septicemia.[5] Campylobacteriosis is typically associated with ingestion of contaminated meat products, however there is some zoonotic risk of pet ownership, as many dogs are asymptomatic shedders of the bacteria.[13]
Other Campylobacter species (C. jejuni) have been clearly linked to causing Guillain-Barre Syndrome, an autoimmune disorder causing muscle weakness and flaccid paralysis.[20] There is less evidence that Guillain-Barre syndrome may be a potential sequela of Campylobacter upsaliensis infection, however C. upsaliensis has been cultured from individuals with Guillain-Barre, indicating that a potential relationship between the two cannot be ruled out.[21]
Virulence[]
Research in the virulence characteristics of this pathogen is currently very limited due to its high susceptibility to the antibiotics commonly used in Campylobacter selective media.[22] A more in-depth knowledge of such knowledge will allow better susceptibility testing, and new antimicrobial therapies to be developed, and help us with the control and spread of this pathogen.
While a dog or cat can be asymptomatic, they may be a carrier and shed the microbe for long periods of time.[23] The transmission of C. upsaliensis occurs by a fecal-oral route; most commonly via contaminated meat, dairy products, and other contaminated food and water sources.[23] Severity of the disease depends on quantity of organisms ingested, other gastrointestinal pathogens present, prior exposure and the immune system of the animal.[23] Since the optimal growth temperature, and pH for Campylobacter species are between 37-42℃, and 6.5-7.5 respectively, the GI tract provides a good environment for its growth.[23]
The characteristic corkscrew motility of C. upsaliensis allows it to dock to the mucus (on enterocytes) before reaching the epithelial cells- it expresses adhesin(s) that recognize mucin on epithelial cells, with which it can gains access to plasma membrane receptors.[24] Via the protein encoded by licABCD gene, it then acquires choline to produce phosphorylcholine which is transferred to lipoteichoic acids thus allowing attachment to epithelial cells.[25] The flagella on Campylobacterfunctions as a type III secretion system to secrete several toxins.[26] One of these toxins has a cytolethal distendingfunction.[27] It is a tripartite toxin that penetrates host epithelial cell nucleus, breaks double stranded DNA, resulting in arrest of cell cycle in G2 phase, increase in host-pathogen contact time, disruption of tight junctions, and increase in overall intestinal permeability.[26] There is no research that shows that this microbe internalizes itself into the host epithelial cells, as part of its virulence.[22]
A typical infection results in inflammation of lamina propria, with an infiltration of neutrophils and mononuclear cells. Lesions are grossly seen as diffuse colonic inflammation.[23] Hemorrhage and edema can therefore be visible on intestines.[26] Acute diarrhea (fluid, mucoid, or bloody feces), vomiting, anorexia and fever can be seen clinically.[23]
Diagnosis[]
Because Campylobacter upsaliensis is considered a commensal bacteria of the gastrointestinal tract in many animals, diagnosis of C. upsaliensis can be cumbersome and laboratory results should be taken into consideration with regards to the context of the patient and other diagnostics.[28] Vomiting, diarrhea, dysentery, fever, and abdominal pain are all common symptoms seen in Campylobacteriosis infections.[2] Ruling out infectious diseases, underlying pathologies of other organ systems with blood chemistry panels, and obstructive disorders with radiographs are all elements of a thorough work-up in these cases.[4] Preliminary diagnostics could include a gram stain fecal smear looking characteristic corkscrew-like motility and gram-negative staining.[29] This only confirms the presence of Campylobacter-like-organisms to warrant further diagnostics.[30] There are many laboratory testing methods that have been implemented for Campylobacter spp. Identification including culture based methods, biochemical testing, immunoassays, and molecular methods such as PCR and whole genome sequencing.[4] Despite the vast array of methods available, no gold standard method of diagnostic test has been agreed upon, and each method has its benefits and drawbacks that should be considered within the scope of each case.[4]
Culture nethods[]
For best isolation results, it is imperative that fecal samples be collected, refrigerated and sent to the diagnostic laboratory as soon as possible to maintain sample integrity.[4] For rectal swabs, Amies or Cary-Blair transport mediums are recommended in order to protect the sample from toxic effects of oxygen on Campylobacter species.[4] Traditionally, filtration methods have been used to help isolate C. upsaliensis with filter pore size of 0.45