ABSTRACT
Diagnosis of feline lungworm, Aelurostrongylus abstrusus, is typically achieved by identifying larvae in feces following concentration through flotation or using the Baermann technique. This work presents observations on the usefulness of an indirect immunofluorescence antibody assay for detection of antibodies to this parasite in the sera of infected cats. Using first-stage larvae of A abstrusus and sera from both experimentally and naturally infected cats, it was determined that the test was fairly sensitive and did not cross-react with serum from an Ancylostoma braziliense (hookworm)-infected cat.
Subject(s)
Antibodies, Helminth/blood , Cat Diseases/parasitology , Fluorescent Antibody Technique, Indirect/veterinary , Immunoglobulin G/blood , Animals , Cat Diseases/blood , Cat Diseases/diagnosis , Cats , Female , Fluorescent Antibody Technique, Indirect/methods , Male , Sensitivity and Specificity , Strongylida/isolation & purification , Strongylida Infections/diagnosis , Strongylida Infections/veterinaryABSTRACT
Because the eggs of Ancylostoma species of dogs and cats are difficult to readily distinguish morphologically, isolation of a certain species often requires the humane death of the source animal or holding an animal after treatment to obtain worms for specific identification or to harvest ex utero eggs. The objective of this study was to obtain an isolate of Ancylostoma braziliense from 1-time, field-collected samples of feline feces without the need for the killing of any animals. During a collection trip to Florida, fecal samples (n â=â 40) were collected and identified as containing A. braziliense eggs (n â=â 26) using centrifugal sugar flotation. Eggs from hookworm-positive slides were washed into tubes, DNA was extracted, and 10 samples were identified as containing A. braziliense using restriction fragment length polymorphism (RFLP) with Hinf1. Six of these samples also contained DNA of Ancylostoma tubaeforme and, thus, only 4 samples were from cats infected only with A. braziliense. Larvae cultured from two of the latter samples were used to subcutaneously inoculate a purpose-bred puppy with the intention to inhibit the growth of any potentially contaminating A. tubaeforme larvae in the culture. The infection was patent at 14 days after inoculation, and the eggs were identified as A. braziliense by RFLP and DNA sequencing. Larvae were cultured from the feces of this dog and used to infect a laboratory-reared, specific-pathogen-free cat; the eggs and larvae produced by the cat were also identified molecularly as those of A. braziliense. The larvae from this cat were used to infect other cats to maintain the isolate for further research. Both the puppy and the first cat used in this study were treated to clear their infections and have since been adopted by new owners.
Subject(s)
Ancylostoma/isolation & purification , Ancylostomiasis/veterinary , Cat Diseases/parasitology , Ancylostoma/classification , Ancylostoma/genetics , Ancylostomiasis/parasitology , Animals , Cats , DNA, Helminth/chemistry , DNA, Helminth/isolation & purification , Feces/parasitology , Polymerase Chain Reaction/veterinary , Polymorphism, Restriction Fragment Length , Sequence Alignment/veterinary , Specific Pathogen-Free OrganismsABSTRACT
The establishment of cat- and dog-derived laboratory strains of Ancylostoma braziliense allowed for a morphological comparison of the eggs of A. braziliense, Ancylostoma caninum, and Ancylostoma tubaeforme. The length, width, and perimeter were determined for images of 10 eggs each of A. braziliense from the feces of a dog infected with a canine isolate and a cat infected with a feline isolate, A. caninum from dog feces, and A. tubaeforme from cat feces. The specific identity of the eggs was verified by polymerase chain reaction and restriction fragment length polymorphism by using HinfI and RsaI restriction digests followed by gel electrophoresis and sequencing. The mean (±SD) length, width, and perimeter and the length-to-width ratio (±SD) (all measurements are in micrometers) for the eggs of each species were as follows: A. braziliense eggs (combined cat and dog source), 53.03 ± 2.33, 36.37 ± 1.35, 140.43 ± 2.56, and 1.46 ± 0.11; A. caninum eggs, 63.92 ± 5.28, 39.21 ± 1.52, 161.99 ± 9.30, and 1.63 ± 0.13; and A. tubaeforme eggs, 61.44 ± 3.05, 39.14 ± 1.40, 157.98 ± 5.81, and 1.57 ± 0.08. The eggs of A. braziliense were significantly (P < 0.001) smaller than the eggs of A. caninum and A. tubaeforme in all dimensions. Thus, the eggs seem to be readily distinguishable using light microscopy, thereby aiding in species identification in fecal samples for a more comprehensive clinical picture and assessment of zoonotic risk.
Subject(s)
Ancylostoma/classification , Ancylostomiasis/veterinary , Cat Diseases/parasitology , Dog Diseases/parasitology , Analysis of Variance , Ancylostoma/genetics , Ancylostoma/ultrastructure , Ancylostomiasis/parasitology , Animals , Cats , Dogs , Feces/parasitology , Ovum/ultrastructure , Polymerase Chain Reaction/veterinary , Polymorphism, Restriction Fragment Length , Restriction Mapping/veterinary , United StatesABSTRACT
A convenience sampling of fecal specimens from 40 cats in northern Florida was examined for the presence of Ancylostoma braziliense eggs by using centrifugal sugar flotation and polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). Of the 40 samples, 26 (65%) contained hookworm eggs. DNA from 24 samples was successfully amplified using PCR; using RFLP, 10 samples were identified as containing DNA of A. braziliense (41.7% of the 24 samples that successfully amplified). Of these, 6 samples contained DNA of both Ancylostoma tubaeforme and A. braziliense, and 4 samples contained only DNA of A. braziliense. The remaining samples (n â=â 14) contained only the DNA of A. tubaeforme, except for 1 sample that had no discernible bands after RFLP.
