scholarly journals Endoparasites of Domesticated Animals That Originated in the Neo-Tropics (New World Tropics)

2019 ◽  
Vol 6 (1) ◽  
pp. 24 ◽  
Author(s):  
Kegan Jones ◽  
Gary Garcia
Keyword(s):  
Meleagris Gallopavo ◽  
Reservoir Host ◽  
Gastrointestinal Parasites ◽  
South American ◽  
Domesticated Animals ◽  
South American Camelids ◽  
The Past ◽  
Lama Glama ◽  
Free Ranging ◽  
Lama Pacos

This review serves to summarize parasites found in Domesticated animals which were found in the Neo-Tropics. Indigenous domesticated Neo-tropical animals include South American camelids, (Lama gunacoa, Lama glama, Lama pacos, Vicuna vicuna), guinea pigs (Cavia porcellus), chinchillas (Chinchilla lanigera), turkeys (Meleagris gallopavo) and ducks (Cairina moschata, Anas platyrhynchos, Dendrocyga autumnalis). These animals were chosen due to their origin of existence (Neo-tropics) and over time these animals became domesticated and were distributed throughout the world. Over eighty (80) references were collected for this review and the papers spanned over eighty (80) years from 1934 to 2018. The gastrointestinal parasites reported for each animal were tabulated and their effects in the animal noted. Parasites reported in domesticated Neo-tropical animals had little to no effect on wild and free ranging animals with a few cases of illness and decreased productivity. The majority of articles viewed these animals as reservoir host which can infect humans and other domesticated livestock. It must also be noted that research done in the past did not focus on the effect these parasites had on these animals but only observed their potential as reservoirs for parasitic diseases.

Plasma biochemical values in the guanaco (Lama guanicoe) compared with the sheep

1997 ◽  
Vol 1997 ◽  
pp. 166-166
Author(s):  
M.D. Fraser ◽  
J.M. Moorby ◽  
D.H. Baker ◽  
J.K.S. Tweed
Keyword(s):  
South American ◽  
Reference Ranges ◽  
Physiological Changes ◽  
Lama Guanicoe ◽  
South American Camelids ◽  
Livestock Species ◽  
Serum Biochemical ◽  
Lama Glama ◽  
Established Technique ◽  
Lama Pacos

The use of metabolic profiles in livestock species is a well established technique for monitoring physiological changes, and determining the health status of individual animals. While reference ranges for serum biochemical values in llamas (Lama glama) (Lassen et al, 1986; Fowler and Zinkl, 1989) and alpacas (Lama pacos) (Simons, Waldron and Hennessy, 1993) have been published, equivalent data for guanacos (Lama guanicoe) are negligible. None of the studies which report values for metabolites in the blood of South American camelids have included a direct comparison with conventional livestock species. The aim of this study was to establish baseline ranges for metabolites in the blood of healthy guanacos, and to compare these with equivalent data for sheep.

267 EFFECT OF SEMINAL PLASMA IN LAMA GLAMA SPERM

2015 ◽  
Vol 27 (1) ◽  
pp. 223 ◽  
Author(s):  
M. Carretero ◽  
F. Fumuso ◽  
M. Miragaya ◽  
C. Herrera ◽  
S. Giuliano
Keyword(s):  
Sperm Motility ◽  
Seminal Plasma ◽  
Membrane Integrity ◽  
South American ◽  
South American Camelids ◽  
Progressive Motility ◽  
Coomassie Blue ◽  
Blue Stain ◽  
Lama Glama ◽  
Motility Of Sperm

In South American camelids, raw semen only presents sperm with oscillatory movements. Therefore, it is necessary to treat these cells to enable them to acquire progressive motility. The effects of raw seminal plasma (SP) on sperm movement patterns (oscillatory, progressive, and hyperactive) have apparently not yet been reported. The objective of this study was to determine effects of raw seminal plasma on sperm motility, viability, and acrosomal status in fresh llama semen. A total of 15 ejaculates were collected (electroejaculation) from 5 llamas (n = 5, r = 3). Each ejaculate was diluted 4 : 1 in 0.1% collagenase in HEPES-TALP (HT) medium and incubated 4 min at 37°C, with the objective of separating spermatozoa from SP. Immediately after incubation, each ejaculate was divided into 2 and centrifuged for 8 min at 800 × g. Pellets were resuspended in either HT or raw SP and maintained at 37°C until evaluation (at 0, 1.5, and 3 h). Sperm motility was evaluated using a phase contrast microscope and a warm stage. Propidium iodide and carboxyfluorescein diacetate were used for assessing membrane integrity (viability). Acrosomal status was evaluated with the Coomassie blue stain. A split-plot design was used with treatment as a factor, with 2 levels (HT and SP) and time as the other factor, with 3 levels (0, 1.5, and 3 h), and blocked by males. There was no significant interaction between treatments (HT and SP) and times (0, 1.5, and 3 h) for each of the seminal characteristics evaluated. Progressive sperm motility was observed after collagenase treatment in all samples. Progressive motility disappeared immediately after the addition of raw SP and showed only oscillatory movements. In contrast, samples incubated in HT maintained progressive motility and became hyperactive. There were no differences (P > 0.05) in total motility of sperm incubated in HT among incubation times (0 h: 30.8 ± 18.9%; 1.5 h: 26.5 ± 11.5%; and 3 h: 21.5 ± 13.5%). However, in samples incubated with SP, a decrease (P < 0.05) in total sperm motility was detected after 3 h of incubation (0 h: 16.5 ± 12.6%, 3 h: 2.3 ± 3.2%). Sperm viability was not different (P > 0.05) between treatments (HT and SP); samples incubated in HT retained 78.4% of the initial viability (32.8/41.8, 3 h/0 h), and samples incubated in SP retained 69.7% of their initial viability (24.4/35.0, 3 h/0 h). The percentage of spermatozoa with intact acrosomes was not different (P > 0.05) between treatments (HT and SP); however, the percentage of sperm with intact acrosomes decreased after 3 h of incubation in both samples (HT and SP). Due to the presence of a high percentage of progressive and hyperactive motile sperm in samples incubated in HT and their absence in samples incubated in SP, we concluded that raw seminal plasma preserved oscillatory sperm motility. Further studies are needed to understand the effects of SP on South American camelid spermatozoa.

Ciliate protozoa of the forestomach of llamas (Lama glama) and alpacas (Vicugna pacos) from the Bolivian Altiplano

Zootaxa ◽  
2008 ◽  
Vol 1703 (1) ◽  
pp. 62 ◽  
Author(s):  
IGNACIO DEL VALLE ◽  
GABRIEL DE LA FUENTE ◽  
MANUEL FONDEVILA
Keyword(s):  
Stomach Contents ◽  
Host Record ◽  
South American ◽  
New Host ◽  
La Paz ◽  
South American Camelids ◽  
New Host Record ◽  
Vicugna Pacos ◽  
Lama Glama ◽  
Ciliate Protozoa

Protozoal diversity in the forestomach of South American camelids (SAC) was studied in eight llamas and six alpacas from the Parque Natural Condoriri (3900 to 4100 m altitude, Departamento La Paz, Bolivia). Total protozoal concentrations were 3.6 times higher (P < 0.001) in the stomach contents of alpacas (39.6 x 10 4 ml -1 and 143.8 x 10 4 ml -1 in llamas and alpacas, respectively). Four to 11 species, all from the genus Entodinium, were observed in llamas, whereas from eight to nine species of Entodinium and minor proportions of Diplodinium (D. anisacanthum, D. dogieli, D. rangiferi), Eudiplodinium (E. bovis, E. maggii, E. neglectum) and Epidinium (E. ecaudatum) were observed in alpacas. The presence of Epidinium species in the alpaca is a new host record. The vestibuliferids, Dasytricha and Isotricha were absent from the forestomach of SAC, as well as other species such as Caloscolex genus, Diplodinium cameli and Entodinium ovumrajae, commonly found in Old World camelids.

157 FIRST IN VITRO EMBRYO PRODUCTION IN ALPACAS (LAMA PACOS)

2009 ◽  
Vol 21 (1) ◽  
pp. 177 ◽  
Author(s):  
G. Gamarra ◽  
E. Huaman ◽  
S. León ◽  
M. Carpio ◽  
E. Alvarado ◽  
...  
Keyword(s):  
South American ◽  
Cleavage Rate ◽  
Embryo Production ◽  
South American Camelids ◽  
Nitrogen Vapor ◽  
Epidermal Growth ◽  
Thermos Flask ◽  
In Vitro Embryo Production ◽  
Lama Pacos

The objective was to produce alpaca embryos in laboratory due to its potential role for the multiplication of genetically superior animals and for conservation purposes. Ovaries were collected from an alpaca abattoir located in the Central Highlands of Peru and transported in a thermos flask with warm saline and antibiotics to the laboratory located 200 km away on the coast. Alpaca epididymal sperm to be used for fertilization was previously frozen by diluting in a TRIS-Fructose based extender with 10% glycerol and frozen as pellets in liquid nitrogen vapor. From 31 ovaries, 262 cumulus–oocyte complexes (COCs) were collected (mean of 8.5 COCs per ovary) which were matured in TCM-199 supplemented with 10% heat inactivated FCS plus epidermal growth factor (EGF), FSH, LH, estradiol, and cysteamine for 30 h incubation at 38.5°C, 5% CO2 and 90% humidity. The selected oocytes post-maturation were fertilized with the frozen/thawed sperm that was subjected post-thawing to Percoll gradient (90 and 45% Percoll), centrifugation and resuspension in TALP-IVF medium supplemented with 20 μm D-penicillamine, 10 μm hypotaurine, 1 μm epinephrine and 1.1 μg mL–1 of heparin. The oocytes were inseminated with a concentration of 10 × 106 spermatozoa per drop of 100 mL of fertilization medium containing 30 oocytes each and incubated for 24 h at 38.5°C, 5% CO2 and 90% humidity. The presumptive zygotes were transferred to 200 μL drops (30 zygotes per drop) of SOFaa media supplemented with 5% heat-inactivated FCS which was replaced by SOFaa plus 1% heat-inactivated FCS on day 5 after fertilization. The incubation period post-fertilization was up to day 7 at 38.5°C, 5% CO2 and 90% humidity, when the embryos were inspected and graded. The cleavage rate was evaluated at 72 h post-fertilization and embryo development was evaluated on day 5 and 7 post-fertilization. The cleavage rate was 27.1% (71/262) and the percentage of oocytes that reached the stage of morula and blastocyst was 8.0% (21/262). The percentage of blastocyst that hatched when incubated after day 7 was 14.28% (3/21). The in vitro embryo production in alpacas was successful and suggests the possibility for application in intensive reproduction for conservation of South American camelids and for genetic improvement. Research was partially funded by contributions of BIONICHE and SAIS TUPAC AMARU, Junin, Peru.

Sarcocystis masoni, n. sp. (Apicomplexa: Sarcocystidae), and redescription of Sarcocystis aucheniae from llama (Lama glama), guanaco (Lama guanicoe) and alpaca (Vicugna pacos)

Parasitology ◽  
2016 ◽  
Vol 143 (5) ◽  
pp. 617-626 ◽  
Author(s):  
GASTÓN MORÉ ◽  
CRISTIAN REGENSBURGER ◽  
M. LAURA GOS ◽  
LAIS PARDINI ◽  
SHIV K. VERMA ◽  
...  
Keyword(s):  
18S Rrna ◽  
18S Rrna Gene ◽  
Rrna Gene ◽  
South American ◽  
Lama Guanicoe ◽  
South American Camelids ◽  
Vicugna Pacos ◽  
Considerable Confusion ◽  
Lama Glama ◽  
Sarcocyst Wall

SUMMARYThere is considerable confusion concerning the species of Sarcocystis in South American camelids (SAC). Several species names have been used; however, proper descriptions are lacking. In the present paper, we redescribe the macroscopic sarcocyst forming Sarcocystis aucheniae and describe and propose a new name, Sarcocystis masoni for the microscopic sarcocyst forming species. Muscles samples were obtained from llamas (Lama glama) and guanacos (Lama guanicoe) from Argentina and from alpacas (Vicugna pacos) and llamas from Peru. Individual sarcocysts were processed by optical and electron microscopy, and molecular studies. Microscopic sarcocysts of S. masoni were up to 800 µm long and 35–95 µm wide, the sarcocyst wall was 2·5–3·5 µm thick, and had conical to cylindrical villar protrusions (vp) with several microtubules. Each vp had 11 or more rows of knob-like projections. Seven 18S rRNA gene sequences obtained from sarcocysts revealed 95–96% identity with other Sarcocystis spp. sequences reported in the GenBank. Sarcocysts of S. aucheniae were macroscopic, up to 1·2 cm long and surrounded by a dense and laminar 50 µm thick secondary cyst wall. The sarcocyst wall was up to 10 µm thick, and had branched vp, appearing like cauliflower. Comparison of the 11 sequences obtained from individual macroscopic cysts evidenced a 98–99% of sequence homology with other S. aucheniae sequences. In conclusion, 2 morphologically and molecularly different Sarcocystis species, S. masoni (microscopic cysts) and S. aucheniae (macroscopic cysts), were identified affecting different SAC from Argentina and Peru.

Anaemia in a llama (Lama glama): treatment, regeneration and differential diagnoses

2018 ◽  
Vol 6 (3) ◽  
pp. e000638 ◽  
Author(s):  
Matthias Gerhard Wagener ◽  
Lucie Marie Grimm ◽  
Martin Ganter
Keyword(s):  
Blood Transfusion ◽  
Packed Cell Volume ◽  
Severe Anaemia ◽  
Common Finding ◽  
South American ◽  
Veterinary Clinic ◽  
South American Camelids ◽  
General Weakness ◽  
Lama Glama ◽  
Lateral Recumbency

Anaemia is a common finding in South American camelids presented to the veterinary clinic. This report describes the case of a llama presented with general weakness and pale conjunctives, displaying severe anaemia with a Packed Cell Volume (PCV) of 6 per cent and suffering from haemonchosis. The animal was presented in lateral recumbency before being treated with whole blood transfusion. After administering a total volume of 850-ml blood, the clinical condition improved remarkably. Regeneration of the haematological parameters required several weeks, PCV increased from 6 per cent on day 0 to 23 per cent on day 28.

scholarly journals Widespread Infection with Hemotropic Mycoplasmas in Free-Ranging Dogs and Wild Foxes Across Six Bioclimatic Regions of Chile

2021 ◽  
Vol 9 (5) ◽  
pp. 919
Author(s):  
Sophia Di Cataldo ◽  
Aitor Cevidanes ◽  
Claudia Ulloa-Contreras ◽  
Irene Sacristán ◽  
Diego Peñaloza-Madrid ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Mixed Models ◽  
Rhipicephalus Sanguineus ◽  
Species Group ◽  
South American ◽  
Adult Age ◽  
Network Analyses ◽  
Male Sex ◽  
Free Ranging ◽  
Sequence Types

Blood samples of 626 rural dogs, 140 Andean foxes (Lycalopex culpaeus), and 83 South American grey foxes (L. griseus) from six bioregions of Chile spanning 3000 km were screened for Mycoplasma DNA by conventional PCR and sequencing. Risk factors of infection were inferred using Generalized Linear Mixed Models and genetic structure by network analyses. Overall, Mycoplasma haemocanis/Mycoplasma haemofelis (Mhc/Mhf) and Candidatus Mycoplasma haematoparvum (CMhp) observed prevalence was 23.8% and 12.8% in dogs, 20.1% and 7.2% in Andean foxes, and 26.5% and 8.4% in grey foxes, respectively. Both hemoplasmas were confirmed in all the bioregions, with higher prevalence in those where ticks from the Rhipicephalus sanguineus species group were absent. Candidatus M. haematominutum and a Mycoplasma sp. previously found in South American carnivores were detected in one fox each. Although the most prevalent Mhc/Mhf and CMhp sequence types were shared between dogs and foxes, network analysis revealed genetic structure of Mhc/Mhf between hosts in some regions. Male sex was associated with a higher risk of Mhc/Mhf and CMhp infection in dogs, and adult age with CMhp infection, suggesting that direct transmission is relevant. No risk factor was identified in foxes. Our study provides novel information about canine hemoplasmas with relevance in distribution, transmission routes, and cross-species transmission.

2,2-Dialkylacetic Acids -A New Class of Naturally Occurring Lipid Constituents

1995 ◽  
Vol 50 (1-2) ◽  
pp. 123-126 ◽  
Author(s):  
Gottfried Raab ◽  
Jürgen Jacob
Keyword(s):  
Retention Time ◽  
Relative Retention Time ◽  
Methyl Esters ◽  
South American ◽  
Time Data ◽  
New Class ◽  
The Past ◽  
Relative Retention ◽  
Naturally Occurring ◽  
Acetic Acids

Abstract The uropygial gland waxes of the South American red-legged Seriema (Cariama cristata (L., 1766)) were found to be composed of unbranched alcohols and 2,2′-dialkyl-substituted acetic acids which so far have not been found in skin lipids. When used as a chemosystematic character, the occurrence of this lipid class separates the order Cariamiformes (Seriemas) from all other avian orders hitherto investigated, especially from the Gruiformes (cranes and rails) to which they have been tentatively attributed in the past. From the GC retention time data now available for a series of 2-alkyl-substituted fatty acid methyl esters relative retention time indices for other compounds may be predicted.

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