scholarly journals Impact of heat treatment on Dirofilaria immitis antigen detection in shelter dogs

2017 ◽  
Vol 10 (S2) ◽  
Author(s):  
Brian A. DiGangi ◽  
Carly Dworkin ◽  
Jason W. Stull ◽  
Jeanette O’Quin ◽  
Morgan Elser ◽  
...  
2016 ◽  
Vol 19 (10) ◽  
pp. 1013-1016 ◽  
Author(s):  
Jeff M Gruntmeir ◽  
Chris B Adolph ◽  
Jennifer E Thomas ◽  
Mason V Reichard ◽  
Byron L Blagburn ◽  
...  

Objectives To determine whether pretreating diagnostic samples with heat increases the detection of Dirofilaria immitis antigen in adult cats, we evaluated feline serum and plasma samples collected in heartworm-endemic areas of the southern United States. Methods Commercial microtiter well assays for detection of D immitis antigen were used to evaluate serum or plasma samples from 385 shelter and free-roaming cats from the southcentral and southeastern United States before and after heat treatment; commercial antibody tests were performed on a subset of samples. Results Prior to sample heat treatment, 1/220 (0.5%) shelter cats and 4/165 (2.4%) free-roaming cats had detectable D immitis antigen. After heat pretreatment, the detection rate increased to 13/220 (5.9%) and 13/165 (7.9%), respectively. Antibody reactive to D immitis was significantly more common ( P <0.001) in the serum of cats that were antigen positive after heat treatment (10/13; 76.9%) than serum from cats that remained antigen negative after heat treatment (22/163; 13.5%). Conclusions and relevance Heat pretreatment of feline samples increased antigen detection by commercial assays for D immitis and improved overall concordance of antigen and antibody test results in antigen-positive samples in this population. Although further work to investigate the specificity of D immitis antigen assays when using pre-treated samples is warranted, this approach may be useful in the diagnosis of heartworm infection in individual cats and may increase the accuracy of surveys based on antigen detection.


1987 ◽  
Vol 64 (3) ◽  
pp. 76-78 ◽  
Author(s):  
D M VANKAN ◽  
R B ATWELL ◽  
A S BLAKE ◽  
P G BUNDESEN ◽  
D B RYLATT ◽  
...  

2014 ◽  
Vol 7 (1) ◽  
pp. 1 ◽  
Author(s):  
Susan E Little ◽  
Melissa R Raymond ◽  
Jennifer E Thomas ◽  
Jeff Gruntmeir ◽  
Joe A Hostetler ◽  
...  

2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Viktor Szatmári ◽  
Martin Willem van Leeuwen ◽  
Christine Jantine Piek ◽  
Luigi Venco

Abstract Background Dirofilaria 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). Results A 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. Conclusions We 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.


1986 ◽  
Vol 72 (5) ◽  
pp. 737 ◽  
Author(s):  
Gary J. Weil ◽  
Lyndia S. Blair ◽  
Debra Vislocky Ewanciw ◽  
Paul F. Malatesta

2016 ◽  
Vol 225 ◽  
pp. 81-85 ◽  
Author(s):  
L. Ciucă ◽  
M. Genchi ◽  
L. Kramer ◽  
C. Mangia ◽  
L.D. Miron ◽  
...  

2012 ◽  
Vol 50 (No. 11) ◽  
pp. 510-512 ◽  
Author(s):  
V. Svobodova ◽  
Z. Svobodova ◽  
V. Beladicova ◽  
D. Valentova

Dogs from two locations in West Slovakiasuspected to have dirofilariosis were tested with the help of microfilariae detection, histochemical identification of microfilaria species and Dirofilaria immitis specific antigen detection in the blood serum. Six out of the group of 15 dogs from Bratislava region were found positive with Dirofilaria repens microfilariae. In the second location situated farther to the south, near Komarno, 6&nbsp;out of 7 dogs were found positive with D. repens microfilariae and 2 with D. immitis. Serological detection of D. immitis antigen was positive in 3 cases among the dogs from this region, 2 of which were found positive with D. immitis microfilariae simultaneously with D. repens. The infection was asymptomatic in all of the dogs included in the trial.


2017 ◽  
Vol 10 (S2) ◽  
Author(s):  
James Carmichael ◽  
Scott McCall ◽  
Utami DiCosty ◽  
Abdelmoneim Mansour ◽  
Linda Roycroft

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