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D369
- Ureaplasma spp.
Description:
Mycoplasmas (members
of the class Mollicutes) are unique bacteria, being
the smallest self-replicating organisms currently known.
They lack the usual cell wall outer structure of most
other bacteria, have very small amounts of genetic material
(DNA), usually require cholesterol for growth and membrane
function, are filterable through the usual bacteriological
filters (450 nanometers), and are very dependent upon
the host for nutritional support. Important mollicutes
known to cause disease in animals include members of
two genera, Mycoplasma and Ureaplasma. Ureaplasma
urealyticum and Mycoplasma hominis can
be important respiratory pathogens in human neonates.
Other Mycoplasma and Ureaplasma species are pathogenic
for the respiratory tract of an ever-expanding number
of domestic and wild animal hosts, including avian,
bovine, caprine, canine, equine, feline, murine, ovine,
porcine, and reptilian hosts. Mollicutes involved in
respiratory disease are inhabitants of mucous membranes.
Host acquisition usually occurs through direct oral
to oral contact with other infected hosts. Respiratory
infections are also transferred via contact with respiratory
aerosols, fomites from infected animals, or convalescent
carriers. Colonization of the respiratory tract by these
organisms is mediated through attachment to host target
cells, frequently involving specialized attachment proteins
(adhesins) on the organisms.
In canines, Ureaplasma species normally inhabit the
canine urogenital and nasopharyngeal tracts, and can
occasionally cause spontaneous abortion in the bitch.
This may occur if there is an increase in the number
of these organisms in comparison to the other common
organisms also inhabiting the vaginal tract. Under these
conditions, there can be an increase in infertility,
spontaneous abortion resulting in resorption or premature
birth, stillbirth, weak puppies, or neonatal death.
Dogs that are kept in large overcrowded breeding kennels
are at greatest risk for acquiring ureaplasmal infections.
Exacerbation of infection in a host frequently occurs
through intercurrent infections, environmental stress,
or in immune deficiencies.
Diagnosis:
The prevalence of
clinical disease associated with Ureaplasma species
is probably underestimated due to the limitations of
laboratory diagnosis. Ureaplasma spp. are fastidious
organisms requiring vigorously quality-controlled medium
for cultivation and several days of incubation. These
procedures are costly and laborious and typically require
special facilities. The treatment of Ureaplasma spp.
is predicted upon rapid detection of infection. Using
PCR, Ureaplasma spp. can be detected rapidly and accurately
such that treatment may be established in the early
stages of infection. Also, this method avoids the problems
associated with culturing since the bacteria do not
need to be grown in order to confirm their presence
in a sample. The PCR specifically detects the genetic
material of Ureaplasma, thus providing veterinarians
a sensitive and definitive method of diagnosis.
Treatment:
Ureaplasma spp. are
generally susceptible to the macrolides, tetracycline,
chloramphenicol, spiramycin, lincomycin, clidamycin,
nitrofurantoin, and aminoglycoside in vitro. Because
tetracycline and chloramphenicol should not be used
in pregnant animals, erythromycin and lincomycin are
safer, although less effective (Greene C. – Infectious
diseases of the dog and cat. 1998, p 176-177).
Sample:
1. Whole blood (3 ml) in a lavender (EDTA)
top tube.
2. Urine in a sterile container.
Special Handling:
Store samples at 4°C until pick up
or shipment.
Test Code:
D369
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