Helminth Parasites of the Chicken, Gallus Domesticus, in Dallas County, Texas

1933 ◽  
Vol 14 (3) ◽  
pp. 251 ◽  
Author(s):  
F. M. Adams ◽  
S. W. Geiser
2017 ◽  
Vol 18 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Manoel Eduardo da SILVA ◽  
Wendeo Ferreira da SILVEIRA ◽  
Fábio Ribeiro BRAGA ◽  
Jackson Victor de ARAÚJO

SUMMARY Parasites are common in intensive or organics systems destined for chickens, which is more conducive to the emergence of gastrointestinal parasites, favored by direct contact with soil and other organisms. The growing demand for animal protein stimulates an expansion of production systems, increasing the stocking density. Outdoor poultry breeding systems (organic or not) that enable lower population density and higher animal welfare does not exclude these animals the presence of environmental pathogens. The control of gastrointestinal helminthosis in non-organic intensive and extensive systems is accomplished by administering anthelmintics with high cost and results unsatisfactory due to the misuse of drugs with consequent selection parasite strains resistant to chemical bases. This problem stimulate research into alternative control measures. Nematophagous fungi are used by its enzymatic action in controlled conditions and how environmental biocontrolers of larvae of gastrointestinal nematodes of livestock. This study evaluated the capacity of conidia/chlamydospores of nematophagous fungi as Duddingtonia flagrans (AC001 and CG722) and Monacrosporium thaumasium (NF34A) for cross the gastrointestinal tract of domestic chickens (Gallus gallus domesticus), and yours germination after traffic and predatory activity “in vitro” on larvae of Panagrellus spp. Fungi conidia/chlamydospores was identified in feces of chickens at times of 6, 12 and 24 hours after administration and spores viability was found after observing the germination, mycelial growth, followed by production of traps, capture and death of Panagrellus spp larvae in feces. Fungi Nematophagous are alternative control measures, efficient and innovative technology for the biological control of helminth parasites of chickens.


2018 ◽  
Vol 32 (2) ◽  
pp. 19-28
Author(s):  
Janak Raj Subedi ◽  
Tasneem Mujahid ◽  
Bijay Cheetri

This study was aimed to determine the prevalence of intestinal helminth parasites of local chicken (Gallus gallus domesticus) from Lalitpur district, Nepal. It was carried out from February 2014 to March 2015. A total of 125 samples (93 alimentary canals of freshly killed chicken and 32 stool samples from ground and fowl runs) were collected. Out of 93 alimentary canals 17 were collected from free range chicken and 76 were from slaughtered house i.e. from poultry farm chicken. The faecal samples were collected in the sterile vials containing 2.5 percent potassium dichromate. Depending upon the convenience, post mortem examination method, differential floatation method and direct smear method were used for the examination of samples. The present study showed only 40 percent of all the poultry examined as infected. Overall 5 species of nematodes, 1 species of cestode and 4 unidentified species were found to be prevalent in chicken from Lalitpur district. The highest prevalence rate was found with Heterakis gallinarum (22.4%) followed by Capillaria species (16%), Ascaridia galli (10.4%), unidentified species (4.8%) and Raillietina tetragona (4%). Statistically there was a significant difference in the prevalence of helminth species (χ2=33.83; p< 0.05; α=1). Likewise, there was significant difference in the prevalence rate of helminth parasites in free range chicken and poultry chicken (χ2=22.055; p< 0.05; α=1).


Author(s):  
C.D. Fermin ◽  
M. Igarashi

Otoconia are microscopic geometric structures that cover the sensory epithelia of the utricle and saccule (gravitational receptors) of mammals, and the lagena macula of birds. The importance of otoconia for maintanance of the body balance is evidenced by the abnormal behavior of species with genetic defects of otolith. Although a few reports have dealt with otoconia formation, some basic questions remain unanswered. The chick embryo is desirable for studying otoconial formation because its inner ear structures are easily accessible, and its gestational period is short (21 days of incubation).The results described here are part of an intensive study intended to examine the morphogenesis of the otoconia in the chick embryo (Gallus- domesticus) inner ear. We used chick embryos from the 4th day of incubation until hatching, and examined the specimens with light (LM) and transmission electron microscopy (TEM). The embryos were decapitated, and fixed by immersion with 3% cold glutaraldehyde. The ears and their parts were dissected out under the microscope; no decalcification was used. For LM, the ears were embedded in JB-4 plastic, cut serially at 5 micra and stained with 0.2% toluidine blue and 0.1% basic fuchsin in 25% alcohol.


Author(s):  
César D. Fermin ◽  
Dale Martin

Otoconia of higher vertebrates are interesting biological crystals that display the diffraction patterns of perfect crystals (e.g., calcite for birds and mammal) when intact, but fail to produce a regular crystallographic pattern when fixed. Image processing of the fixed crystal matrix, which resembles the organic templates of teeth and bone, failed to clarify a paradox of biomineralization described by Mann. Recently, we suggested that inner ear otoconia crystals contain growth plates that run in different directions, and that the arrangement of the plates may contribute to the turning angles seen at the hexagonal faces of the crystals.Using image processing algorithms described earlier, and Fourier Transform function (2FFT) of BioScan Optimas®, we evaluated the patterns in the packing of the otoconia fibrils of newly hatched chicks (Gallus domesticus) inner ears. Animals were fixed in situ by perfusion of 1% phosphotungstic acid (PTA) at room temperature through the left ventricle, after intraperitoneal Nembutal (35mg/Kg) deep anesthesia. Negatives were made with a Hitachi H-7100 TEM at 50K-400K magnifications. The negatives were then placed on a light box, where images were filtered and transferred to a 35 mm camera as described.


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