Need serology?
Yes, we're still the PCR experts. But now Zoologix also performs ELISA tests...

SRV
Herpes B
SIV
STLV
Measles
Hepatitis A
Hepatitis B
Hepatitis C

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For our international clients:
Our DRY CARDS let you mail samples to Zoologix easily and cheaply from anywhere! Samples on DRY CARDS are small, light and stable at room temp for several weeks.

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Zoologix performs primate tests by PCR for...

Baboon endogenous virus

Baboon cytomegalovirus

Borrelia burgdorferi (Lyme disease)

Campylobacter

Chimpanzee cytomegalovirus

Chlamydia pneumoniae

Chlamydia trachomatis

Clostridium difficile

Clostridium screen

Cryptosporidium

Dengue

Ebola

E. coli O157:H7

E. coli panel

Encephalitis, Japanese

Encephalitis, St. Louis

Encephalomyocarditis (EMCV)

Enterovirus

Epstein-Barr virus

Giardia

Gibbon ape leukemia

Helicobacter

Hepatitis A virus

Hepatitis B virus

Hepatitis C virus

Herpes B virus

Herpes simplex type 1

Herpes simplex type 2

Herpesvirus ateles

Herpesvirus papio 1

Herpesvirus papio 2

Herpesvirus saimiri

Human cytomegalovirus

Human herpesvirus types 6, 7 & 8

Human T cell lymphotropic virus

Human Varicella-Zoster

Influenza

Klebsiella

Lawsonia intracellularis

Lymphocryptovirus

Macaque cytomegalovirus

Malaria

Measles

Monkeypox

Monkey parvoviruses

Mycobacteria

Mycoplasma pneumoniae

Mycoplasma screen

Neisseria gonorhoeae

Neisseria meningitidis

Plasmodium inui

Plasmodium screen

Reovirus screen

Rhesus papillomavirus

Rhesus rhadinovirus

Rotavirus

Salmonella

Shigella and enteroinvasive E. coli

Simian agent 8 (SA8)

Simian cytomegalovirus (SCMV)

Simian foamy virus (SFV)

Simian hemorrhagic fever (SHFV)

Simian immunodeficiency virus (SIV)

Simian retrovirus (SRV)


Clostridium PCR test for primates
primate assay data sheet

Clostridium difficile

Test code:
B0037 - Qualitative detection of Clostridium difficile bacteria by polymerase chain reaction. This assay differentiates pathogenic and non-pathogenic strains of C. difficile by detecting the toxin-producing genes.

Clostridium difficile is a gram positive, anaerobic, spore forming motile rod bacterium that commonly inhabits the intestinal tract of many mammalian species, reptiles and birds. It is also found in the environment. The bacterium is a highly diverse organism, with more than 400 unique types, and has several virulence factors. Exotoxin A and B are the most significant factors, and bacterial production of exotoxins is correlated with pathogenicity of individual strains of C. difficile. Toxin A is an enterotoxin, promoting fluid exudation from the intestinal mucosa, and acts synergistically with the cytotoxic toxin B through attachment to specific receptors on the surface of enterocytes. The combined action of these toxins results in necrosis of superficial epithelium and edema in affected areas of intestine.

The organism is an important cause of enteric disease in laboratory rodents and horses. Hamsters, guinea pigs and mice may be affected by pseudomembranous colitis induced by antimicrobial therapy. In neonatal foals, C. difficile has been associated with hemorrhagic necrotizing enterocolitis and diarrhea. The lack of an established intestinal microflora may make foals more susceptible to colonization by this bacterium. Adult horses may develop typhlocolitis and outbreaks of nosocomially acquired diarrhea have been reported (Donaldson and Palmer, 1999; Madewell et al., 1995; Perrin et al., 1993).

C. difficile has also recently been implicated as a cause of typhlocolitis in nursing piglets, chronic diarrhea in dogs and enterotoxemia in ostriches.

In clinically normal patients, an established intestinal microflora is thought to competitively prevent proliferation of C. difficile and subsequent toxin attachment. Alteration of intestinal microbial balance with antibiotic use and increased exposure to the organism in a hospital setting allows C. difficile to colonize the gut in susceptible individuals.

Bacterial culture of C. difficile is not highly sensitive and does not differentiate the pathogenic and non-pathogenic strains. Specific tests for C. difficile toxins used in the diagnostic laboratory include cell culture, which relies on the presence of biologically active toxin, and an ELISA assay which detects immunologically active toxin that may or may not be biologically active.

PCR detection of C. difficile is highly sensitive and can discriminate between toxigenic and nontoxigenic strains of the organism by specific detection of toxin-producing genes.

Utilities:

  • Confirm the disease causing agent
  • Shorten the time required to confirm a clinical diagnosis of C. difficile infection.
  • Ensure that colonies are free of this bacterium
  • Early prevention of spread of this bacterium
  • Minimize human exposure to this bacterium
  • Safety monitoring of biological products that derive from primates

References:
Donaldson, M.T. and Palmer, J.E. (1999) Prevalence of Clostridium perfringens enterotoxin and Clostridium difficile toxin A in feces of horses with diarrhea and colic. J. Am. Vet. Med. Assoc. 215:358 361.
Madewell, B.R., Tang, Y.J., Jang, S., Madigan, J.E., Hirsh, D.C., Gumerlock, P.H. and Silva, J. (1995) Apparent outbreaks of Clostridium difficile associated diarrhea in horses in a veterinary medical teaching hospital. J. Vet. Diagn. Invest. 7:343 346.
Perrin, J., Cosmetatos, I., Gallusser, A., Lobsiger, L., Straub, R. and Nicolet J. (1993) Clostridium difficile associated with typhlocolitis in an adult horse. J. Vet. Diagn. Invest. 5:99 101.

Specimen requirements: Rectal swab or 1 ml feces, shipped overnight at room temperature.

For specimen types other than those listed here, please call to confirm specimen acceptability and shipping instructions.

For all specimen types, if there will be a delay in shipping, or during very warm weather, refrigerate specimens until shipped and ship with a cold pack unless more stringent shipping requirements are specified. Frozen specimens should be shipped so as to remain frozen in transit. See shipping instructions for more information.

Turnaround time: 2 business days

Methodology: Qualitative PCR

Normal range: Nondetected

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