Abstract
BackgroundDirofilaria immitis is responsible for heartworm disease in dogs in endemic areas worldwide. Screening for this infection is done by blood tests. Antigen testing is the most sensitive method to detect an infection with adult (female) worms. Microscopic examination of a blood smear or Knott’s test can be used to detect circulating microfilariae, the infective larvae. To increase the sensitivity of the antigen test by decreasing the false negative test results, heating of the blood sample has been recommended in recent guidelines. Heating is believed to remove blocking immune-complexes. Circulating microfilariae are not specific findings for heartworm infection, as other nematodes (among others, Acanthocheilonema dracunculoides) can also result in microfilaremia. Although the type of microfilariae cannot be determined by microscopy alone, real-time PCR can reliably identify the infecting nematode species. Correct identification of the parasite is of major importance, as an infection with D. immitis requires antiparasitic therapy, whereas A. dracunculoides is thought to be a clinically irrelevant coincidental finding. The present case report describes a microfilaremic dog where the initial antigen test for D. immitis turned positive after heat treatment, whereas real-time PCR revealed that the microfilariae were A. dracunculoides (syn. Dipetalonema dracunculoides).ResultsA circa 5-year old, asymptomatic Spanish mastiff dog was referred for heartworm therapy because microfilariae were found via a screening blood test. The dog was recently imported to the Netherlands from Spain, where it had been a stray dog. Antigen tests on a plasma sample for D. immitis were performed with three different test kits, which all turned out to be negative. However, heat treatment of two of these samples were carried out and both of them led to a positive antigen test result. Real-time PCR showed that the circulating microfilariae belonged to A. dracunculoides species. Three administrations of moxidectin spot-on at monthly intervals resulted in a negative antigen and a negative Knott’s tests one month after the last treatment.ConclusionsWe conclude that heat treatment of initially negative blood samples for D. immitis could lead to false positive antigen test results if the dog is infected with A. dracunculoides.
Highlights
Dirofilaria immitis is responsible for heartworm disease in dogs in endemic areas worldwide
Recent studies in dogs showed that heat treatment of initially negatively tested plasma samples can increase the sensitivity of Enzyme-linked immunosorbent assay (ELISA) immunoassay, reducing the number of false negative test results [8]
False positive antigen test results have been reported after heat treatment of the blood samples in dogs that were infected with A. vasorum and D. repens [9, 10]
Summary
Dirofilaria immitis is responsible for heartworm disease in dogs in endemic areas worldwide Screening for this infection is done by blood tests. To increase the sensitivity of the antigen test by decreasing the false negative test results, heating of the blood sample has been recommended in recent guidelines. The present case report describes a microfilaremic dog where the initial antigen test for D. immitis turned positive after heat treatment, whereas real-time PCR revealed that the microfilariae were A. dracunculoides Recent studies in dogs showed that heat treatment of initially negatively tested plasma samples can increase the sensitivity of ELISA immunoassay, reducing the number of false negative test results [8]. False positive antigen test results have been reported after heat treatment of the blood samples in dogs that were infected with A. vasorum and D. repens [9, 10]
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