Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 12
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

The aim of this research was to determine rumination time (RT) and the subsequent milk yield, along with trait changes during lactation dependent on the reproductive status of dairy cows. 728 cows were selected for evaluation in regards to 1–150 days of milk production (DIM). According to their period of lactation and reproductive status, the cows were selected for the following groups: Inseminated (1–35 days after insemination, n=182), Open (45–90 days after calving, n=126), Fresh (1–44 days after calving, n=45); Not-pregnant (>35–60 days after inse- mination and not-pregnant, n=55); Pregnant (35–60 days after insemination and pregnant (n=320). The animals were milked with Lely Astronaut® A3 milking robots. The daily milk yield, rumination time, bodyweight, milk composition (fat, protein, lactose, somatic cell count and gynecological status date) were collected from the Lely T4C management program for analysis. We estimated the lowest productivity in the pregnant cows, where the average milk yield was 28.72 kg and the highest productivity in the fresh cow (p<0.001) (Table 1). The longest rumina- tion time was determined for the inseminated cows, statistically significantly higher at 9.92% (p<0.001) than in the non-pregnant cows, whose rumination time was the shortest. The statisti- cally reliably RT positively correlated with productivity (r=0.384, p<0.001) of the cows (from r=0.302 in the second lactation and r=0.471 in the first lactation to r=0.561 in multiparous cows; p<0.001). Rumination time, according to groups of cows by milk yield, had a tendency to increase (2.14 times) from 202.0± 87.38 (in cows with a productivity of less than 10 kg milk) to 431.6±33.91 (in cows with a milk yield higher than 50 kg) by the linear regression equation: y = 38.02x + 232, R² = 0.721 (p<0.001). The relation between the gynecological status and milk fat-protein ratio of the cows was statistically significant (χ2=2.974, df= 8, p <0.0001). The longest rumination time was determined for the inseminated cows (1 – 35 days after insemination), and the shortest for the not-pregnant cows (>35 – 60 days after insemination and not-pregnant). We can conclude that rumination time, subsequent yield, and milk trait change depends on the period of lactation and reproductive status of a dairy cow.

Go to article

Authors and Affiliations

R. Antanaitis
V. Žilaitis
V. Juozaitienė
A. Noreika
A. Rutkauskas
Download PDF Download RIS Download Bibtex

Abstract

Ruminal acidosis is frequent in cattle fattening systems associated with grain-rich fibre-poor diets. This study aimed to assess the prevalence of ruminal lesions compatible with ruminal acidosis intensive fattening farms and its risk factors on farm. Rumens of 218 out of 1960 bullocks from six farms were classified in slaughterhouses, and the management practices and the type of feed were compared. The prevalence of lesions compatible with ruminal acidosis was high (65%), where 47% and 18% of the animals had ruminal lesions compatible with subacute and acute disease, respectively. Prevalence of lesions differed significantly between the farms, with differences in the management and feeding practices. Ruminal lesions compatible with ruminal acidosis are prevalent in cattle fattening units in Portugal and husbandry and feeding practices are likely to have an impact.
Go to article

Authors and Affiliations

J. Vieira
1
R. Matos
1 2
J. Cannas da Silva
1 2
W. Baumgartner
3
S. Van Harten
1 2
A. Dâmaso
1 2

  1. Veterinary Medicine School, University Lusófona of Humanities and Technologies, Campo Grande 376, 1749-024, Lisbon, Portugal
  2. CBIOS - Research Centre for Biosciences & Health Technologies, Campo Grande 376, 1749-024, Lisbon, Portugal
  3. University Clinic for Ruminants, University of Veterinary Medicine, Veterinaerplatz 1, A-1210 Vienna, Austria
Download PDF Download RIS Download Bibtex

Abstract

The objectives of this study were to examine the option of being able to use rumination time (RT) as a form of stress indicator in the first thirty days after calving, and to determine the rela- tionship between rumination time, blood cortisol levels, and lactate concentration levels in dairy cows during the first thirty days after calving.

Ninety cows which produced milk (DIM) within 1-30 days were selected and categorised into the following groups: the first group (1) fell within 1-7 days after parturition (dpp) (n=30); the second group (2) fell within 8-14dpp (n=30); and the third group (3) fell within 15-30dpp (n=30) after calving. The cows were milked using Lely Astronaut® A3 milking robots with free traffic. The blood samples were tested using the fluorescence enzyme immunoassay method for cortisol analysis. Lactate concentrations were tested with a Lactate Pro2 ®.

The RT increased during all of the exploratory periods (with readings between 1.12-4.90%). A decrease was also observed in the lactate levels (by 1.10 times) and cortisol levels (by 1.98 times, p<0.05) of cows which fell within the 8-14dpp group, when compared to an average of 1-7dpp in the previous study period (15-30dpp). However, lactate concentrations increased (by 1.84 times, p<0.05) as well as cortisol levels (by 2.09 times, p <0.01) when compared with a figure between 8-14 dpp on the average. The results obtained indicate that, RT increased during all exploratory periods, while a decrease by 1.10 times and 1.98 times was observed in lactate levels and cortisol levels, respectively. During the entire period of the study RT was positively correlated with the lactate concentration levels, and negatively correlated with cortisol levels. Within a period of 1-14 days, a negative correlation was determined with lactate levels along with a 15-30dpp-positive correlation coefficient. In conclusion, RT can be used as a kind of stress indicator for cows in the first thirty days after calving; however, further research is required to ascertain this conclusion.

Go to article

Authors and Affiliations

D. Malašauskienė
M. Televičius
V. Juozaitienė
R. Antanaitis
Download PDF Download RIS Download Bibtex

Abstract

The objective of this study was to determine the association between subclinical acidosis (SARA) and subclinical ketosis (SCK) with biomarkers from an automatic milking system (AMS) measuring in relation to rumination time (RT), milk yield (MY), bodyweight (BW), milk temperature, the milk fat-to-protein ratio, and the electrical conductivity of milk at the udder quarters-level which can be read in fresh dairy cows. During the course of the study, all of the fresh dairy cows (n=711) were examined according to a general clinical investigation plan. The cows were selected for 1-30 days of milk (DIM) and were milked using Lely Astronaut® A3 milking robots with free traffic. Rumination time shows a statistically significant positive correlation with milk yield (milk temperature) and is negatively correlated with the fat and protein ratio. Healthy cows demonstrated the highest level of rumination time and the lowest milk temperature. The average BW for these cows was 1.64% lower than for the SARA group and the BW kg was 2.10% higher than SCK cows. MY was 14.01% lower in comparison with SARA and 6.42% higher in comparison with SCK. According to these results, some biomarkers from the AMS have an association with SARA and SCK. However, further research with a higher number of cows is needed to confirm this conclusion.

Go to article

Authors and Affiliations

R. Antanaitis
V. Juozaitienė
D. Malašauskienė
M. Televičius
M. Urbutis
Download PDF Download RIS Download Bibtex

Abstract

The aim of this study was to investigate the impact of feed supplements with alfa-amylase and beta-glucanase (Optipartum C+ 200) on ingestive-related behaviour biomarkers registered with real-time sensors: rumination behaviours and reticulorumen parameters (pH and temperature). Cows (n=20) in the treatment group (TG) were fed with Optipartum C+ 200 (Enzymes feed supplement: Alfa-Amylase 57 Units; Beta-Glucanase 107 Units) from 21 days before calving until 30 days after calving with a feeding rate of 200 g/cow/day. Cows (n=22) in the control group (CG) were fed a feed ration without feed supplement. Measurements started from 6 days before calving and continued until 21 days after calving. The following indicators were registered: with the RumiWatch System: Rumination time; Eating time; Drinking time; Rumination chews; Eating chews; Drinking gulps; Bolus; Chews per minute; Chews per bolus. With the SmaXtec system: the temperature, pH of the contents of the cows’ reticulorumens, and cows’ walking activity.
According to our results, feed supplementation with alfa-amylase and beta-glucanase (Optipartum C+ 200) in the TG group resulted in increases in the following parameters: 9% rumination time and eating time, 19% drinking time, 11% rumination chews, 16% eating chews, 13% number of boluses per rumination, 5% chews per minute and 16% chews per bolus. The rumination time showed a strong, positive relation with rumination chews and bolus indicators in both groups (TG and CG) (p<0.001); while the rumination time in both groups of cows showed an opposite direction and was negatively related to eating time and eating chews (p<0.05).
We found a 1.28 % lower reticulorumen pH and a 0.64 % lower reticulorumen temperature in cows fed with the supplement compared with cows in the control group. Cows in TG were 8.80% more active than those in the CG group. For improvement of ingestive-related behaviour we suggest adding a feed supplement with alfa-amylase and beta-glucanase (Optipartum C+ 200).
Go to article

Authors and Affiliations

R. Antanaitis
1
L. Anskienė
2
M. Televičius
1
D. Malašauskienė
1
G. Šertvytytė
1
R. Stoškus
3
E. Meškinytė
4
J. Rous
4
B. Helm
4

  1. Large Animal Clinic, Veterinary Academy, Lithuanian University of Health Sciences, Tilžės str 18, LT-47181 Kaunas, Lithuania
  2. Department of Animal Breeding, Veterinary Academy, Lithuanian University of Health Sciences, Tilžės str 18, LT-47181 Kaunas, Lithuania
  3. Republican Veterinary Supply Center JSC, Raudondvaris str. 131B, LT-47191, Kaunas, Lithuania
  4. Animal Husbandry Selections, Breeding Values and Dissemination Center, Agriculture Academy, Vytautas Magnus University, Universiteto St. 10A, Akademija, LT-53361 Kaunas distr., Lithuania
Download PDF Download RIS Download Bibtex

Abstract

The present study aimed to evaluate the efficiency of hypertonic saline solution (HSS) as a novel treatment of acute ruminal lactic acidosis (ARLA) in cattle, focusing on urinary excretion of acids. Twelve cannulated steers were submitted to experimentally induced ARLA by adminis- tering sucrose into the rumen. Twenty hours later, the cattle were randomly divided into two equal groups. The first group was treated with 7.5% HSS (5 mL/kg) over 15 min, and isotonic saline solution (ISS; 20 mL/kg) for the subsequent 165 minutes. The control group was administered ISS instead of HSS. Rumen and urine samples were collected at different times during the experiment from the baseline to 64 h post-induction. The induction caused a medium-to-moderate ruminal acidosis, and a moderate degree of systemic acidosis and dehydration. Steers treated with HSS increased by 50% its glomerular filtration rate (1.61 mL/min) compared to ISS group (1.06 mL/ min; p<0.03). The overall volume of urine excreted by HSS group was higher than that in ISS group (1.62 L vs 0.7 L; p<0.02). This increase in total volume of urine provided by HSS favored a greater excretion of H+ ions in urine, which was 3.39-fold higher in HSS group (64.3*10-7 vs 18.9*10-7 Mol) as well as lactate (241.7 vs 181.8 mMol) and P urinary excretion (3.8 vs 1.1 mMol) that reduced the urine pH (5.3 vs 5.7). Only the HSS group decreased significantly blood total lactic acid concentration (20.3 %) throughout the treatment. A positive relationship was found between the excretion of urinary phosphorus and urinary pH (r2=0.562). The results showed that this novel treatment with HSS enhanced renal excretion of acids and may be recommended as an additional treatment for cattle with lactic acidosis.

Go to article

Authors and Affiliations

F.A.M.L. Rodrigues
A.H.H. Minervino
R.A. Barrêto Júnior
L.F. Reis
R.N.F. Ferreira
C.S. Mori
F.L.C. Oliveira
R.S. Sousa
Download PDF Download RIS Download Bibtex

Abstract

Small ruminant lentivirus (SRLV), which causes caprine arthritis encephalitis in goats and ovine progressive pneumonia (maedi-visna disease) in sheep, is classified in genus Lentiviruses belonging to Retroviridae family. It persists in infected goats and sheep, which mostly are sub- clinical. A serological survey was conducted to determine the prevalence of small ruminant lentivirus infection in Thai goat population. Serum samples were taken from 1,925 goats distributed throughout the country, then they were tested for the presence of SRLV antibodies using commer- cial indirect enzyme-linked immunosorbent assay (ELISA) test kits. Results revealed that a total of 68 goats were found seropositive, representing the apparent prevalence and true prevalence of 3.57% and 2.60%, respectively. The seroprevalence, revealed in this study, was lower than in the previous reports. The decreasing of seroprevalence might be caused by successful control strategies from Department of Livestock Development (DLD).
Go to article

Authors and Affiliations

T. Mongkonwattanaporn
1
P. Lertwatcharasarakul
2
P. Intaravichai
3
T. Rukkwamsuk
1

  1. Department of Large Animal and Wildlife Clinical Sciences, Faculty of Veterinary Medicine, Kasetsart University, 1 Moo 6, Malaiman Road, Kamphaeng Saen, Nakhon Pathom 73140, Thailand
  2. Department of Pathology, Faculty of Veterinary Medicine, Kasetsart University, 1 Moo 6, Malaiman Road, Kamphaeng Saen, Nakhon Pathom 73140, Thailand
  3. Faculty of Veterinary Medicine and Applied Zoology, HRH Princess Chulabhorn Collage of Medical Science, Chulabhorn Royal Academy, 906 Kamphaeng Phet 6 Road, Talat Bang Khen, Lak Si, Bangkok 10210, Thailand
Download PDF Download RIS Download Bibtex

Abstract

This study aims to investigate how grazing is perceived across the Curvature Subcarpathians (Romania) by farmers. We investigate farmers’ attitudes toward and understanding of grazing practice and associated processes involving small ruminants (sheep and goats). Additionally, we review the scientific literature and new discussions about grazing vs overgrazing terms and changes in the Romanian small ruminant livestock. Results of the survey on the total of 101 case studies from villages in 3 counties (Damboviţa, Buzau, and Vrancea) show that: (i) grazing is differently perceived; (ii) most of the areas designated for grazing are located near riverbanks (over 55%); most of the respondents reported that the areas intended for grazing are quite close to the inhabited areas; distances are less than 2.5 km; and over 60% of respondents believe that the areas are continuously subject to soil degradation processes; (iii) answers given in connection with the issues addressed provide both relevance to the Curvature Subcarpathians (6792 km2) and the potential impact of higher pressure of grazing on local areas due to the discouragement of specific transhumance policies (more than 60% required subsidies). The average stocking density is about 4.7 head per ha. In general, beyond different farmers’ perceptions, a scientific question remains open regarding the quantitative impact of grazing on hydrological processes. Hence, a field survey (e.g., rainfall-runoff experiments) to assess grazing pressure on water and soil resources will be performed.
Go to article

Authors and Affiliations

Gianina Neculau
1 2
ORCID: ORCID
Gabriel Minea
1 2
ORCID: ORCID
Nicu Ciobotaru
1 2
ORCID: ORCID
Gabriela Ioana-Toroimac
3
ORCID: ORCID
Sevastel Mircea
1
ORCID: ORCID
Oana Mititelu-Ionuș
4
ORCID: ORCID
Jesús Rodrigo-Comino
5
ORCID: ORCID

  1. University of Bucharest, Research Institute of the University of Bucharest, 90 Panduri Street, Sector 5, 050107, Bucharest, Romania
  2. National Institute of Hydrology and Water Management, 97 E Bucureşti – Ploieşti Road, Sector 1, 013686, Bucharest, Romania
  3. University of Bucharest, Faculty of Geography, Bucharest, Romania
  4. University of Craiova, Faculty of Sciences, Department of Geography, Craiova, Romania
  5. University of Granada, Faculty of Philosophy and Letters, Department of Regional Geographic Analysis and Physical Geography, Granada, Spain
Download PDF Download RIS Download Bibtex

Abstract

The study was conducted on 26 male, 30 days-old goats, separated from their mothers, divided into two equal groups: I - control and II - experimental, consisting of 13 animals each. All animals were fed with milk replacer, experimental group received additionally 50 g/kg body weight, additive of HMB, for 60 days. The following features were analyzed: body weight, daily increases of body weight, as well as hematological and biochemical blood features. Differences in body weight were found, between experimental and control group, after 60 days of experiment 0.57 kg (p≤0.01). The daily weight gain of experimental animals was higher in comparison with control group. Significant differences were also noted in results of hematological and biochemical blood parameters. Experimental animals showed a higher level of red blood cells as well as number of lymphocytes in comparison with the control group, (p≤0.01).Significant changes were also observed in the level of triglycerides, inorganic phosphorus and protein between both groups. The acid-base balance parameters and ionogram, showed a higher pH level (p≤0.05) HCO – act., HCO – std., BE, ctCO , O sat, K+, Cl– (p≤0.01), while the anion gap (AG) and Na+ were significantly lower in control group (p≤0.01).

Go to article

Authors and Affiliations

K. Cebulska
P. Sobiech
S. Milewski
K. Ząbek
Download PDF Download RIS Download Bibtex

Abstract

Crimean Congo Hemorrhagic Fever (CCHF) is an important disease. The objective of this study was to investigate the presence / prevalence of CCHFV in tick and milk and blood samples of domestic ruminant (cattle, sheep and goat) in Resadiye town of Tokat province, where the disease is endemic. Although no virus RNA was found from whole blood and milk samples, it was detected in 10 of 78 (12.8%) tick pools. Viral loads ranged from 4.8x104 copies/ml to 2.66x109 copies/ml. Out of 171 serum samples examined, 113 (66.1%) were found to be positive for CCHFV. In conclusion, it was revealed that the prevalence of CCHFV was more common in small ruminants than in cattle. It is an important result in terms of public health that virus cannot be detected. The detection of virus RNA in tick samples shows that CCHFV is still endemic in domestic animals.

Go to article

Authors and Affiliations

T. Özüpak
H. Albayrak
Download PDF Download RIS Download Bibtex

Abstract

Neospora caninum ( N. caninum) is the etiologic agent of neosporosis, a potential cause of severe reproductive disorders in cattle, small ruminants, equines, wild animals and canids across the world. The current study is performed to estimate molecular prevalence of N. caninum in small ruminants and equines that had abortion in Kurdistan region of Iraq. A total of 64 tissue samples (brain, placenta, heart, lung and liver) were taken from aborted foetuses, with a total of 122 dam blood samples taken from 63 sheep, 39 goats, 12 mares and 8 jennies in local breed fields. Besides, a risk factor analysis for N. caninum positive animals was performed. The observed prevalence of N. caninum DNA in the blood of sheep, goats, horses and donkeys were 20.6%, 17.9%, 21.4% and 25.0%, respectively, and 19.3%, 17.6%, 18.1 and 20.0% in the aborted foetuses of the animals, respectively. Moreover, occurrence of N. caninum was 20.3% in the blood of aborted dams, while it was 18.7% in their aborted foetuses. Confirmatory analysis was also done through constructing a phylogenetic tree to compare the partial sequences of the Nc-5 gene in our isolates (OP771519, OP771520, OP771521 and OP771522) with the GenBank sequences. This showed 98-100% sequence identity with other N. caninum strains in the GenBank database. Older small ruminants and equines had a higher risk of being positive for N. caninum and exposure to dogs were considered as significant risk factors for N. caninum infection in the studied animals (p<0.05). Thus, the results of this study suggest that N. caninum is one of the microbial abortive agents in small ruminants and equines in Kurdistan region of Iraq. It is hoped that the results of this study will help to control animal abortion in livestock and reduce the economic losses.
Go to article

Bibliography

  1. Ahmed NE, Al-Akabway LM, Ramadan MY, El-Gawad SM, Moustafa MM (2017) Serological and PCR-sequencing assays for diagnosis of Toxoplasma gondii and Neospora caninum infecting camels in Egypt. Benha Vet Med J 33: 200-210.
  2. AL-Badrani BA, AL-Farwachi MI, AL-Hankawai OK (2012) Detection of Toxoplasma gondii and Neospora caninum antibodies in cattle in Mosul city, Iraq. Al-Qadisiyah J Vet Med Sci 11: 46-50.
  3. Al-Farwachi MI, Al-Badrani BA, Al-Khafaji WS (2018) Serodiagnosis of ovine neosporosis in Mosul city , Iraq. Eurasian J Vet Sci 28: 190-193.
  4. Al-Farwachi MI, Al-Hankawe OK, Al-Khafaji WS (2012) Serodiagnosis of Bovine Neosporosis in Mosul City, Iraq. Assiut Vet Med J 58: 1-4.
  5. Al-Shaeli SJ, Ethaeb AM, Gharban HA (2020) Molecular and histopathological identification of ovine neosporosis (Neospora caninum) in aborted ewes in Iraq. Vet World 13: 597-603.
  6. Almería S, Serrano-Perez B, Darwich L, Domingo M, Mur-Novales R, Regidor-Cerrillo J, Cabezón O, Pérez-Maillo M, Lopez-Helguera I, Fernández-Aguilar X, Puig-Ribas M, Ortega-Mora LM, García-Ispierto I, Dubey JP, López-Gatius F (2016) Foetal death in naive heifers inoculated with Neospora caninum isolate Nc-Spain7 at 110 days of pregnancy. Exp Parasitol 168: 62-69.
  7. Amdouni Y, Abedennebi I, Amairia S, Abdelkader A, Chandoul W, Gharbi M (2022) First molecular detection of Neospora caninum from naturally infected slaughtered camels in Tunisia. Vet Med Sci 8: 2241-2247.
  8. Amdouni Y, Rjeibi MR, Awadi S, Rekik M, Gharbi M (2018) First detection and molecular identification of Neospora caninum from naturally infected cattle and sheep in North Africa. Transbound Emerg Dis 65: 976-982.
  9. Anderson JA, Alves DA, Cerqueira-Cézar CK, da Silva AF, Murata FH, Norris JK, Howe DK, Dubey JP (2019) Histologically, immunohistochemically, ultrastructurally, and molecularly confirmed neosporosis abortion in an aborted equine fetus. Vet Parasitol 270: 20-24.
  10. Antonello AM, Pivoto FL, Camillo G, Braunig P, Sangioni LA, Pompermayer E, Vogel FS (2012) The importance of vertical transmission of Neospora sp. in naturally infected horses. Vet Parasitol 187: 367-370.
  11. Bartley PM, Guido S, Mason C, Stevenson H, Chianini F, Carty H, Innes EA, Katzer F (2019) Detection of Neospora caninum DNA in cases of bovine and ovine abortion in the South-West of Scotland. Parasitol 146: 979-982.
  12. Bártová E, Sedlák K, Kobédová K, Budíková M, Joel Atuman Y, Kamani J (2017) Seroprevalence and risk factors of Neospora spp. and Toxoplasma gondii infections among horses and donkeys in Nigeria, West Africa. Acta Parasitol 62: 606-609.
  13. Basso W, Holenweger F, Schares G, Müller N, Campero LM, Ardüser F, Moore-Jones G, Frey CF, Zanolari P (2022) Toxoplasma gondii and Neospora caninum infections in sheep and goats in Switzerland: Seroprevalence and occurrence in aborted foetuses. Food Waterborne Parasitol 28: e00176.
  14. Basso W, Venturini L, Venturini MC, Hill DE, Kwok OCH, Shen SK, Dubey JP (2001) First isolation of Neospora caninum from the feces of a naturally infected dog. J Parasitol 87: 612-618.
  15. Beck HP, Blake D, Dardé ML, Felger I, Pedraza-Díaz S, Regidor-Cerrillo J, Gómez-Bautista M, Ortega-Mora LM, Putignani L, Shiels B, Tait A, Weir W (2009) Molecular approaches to diversity of populations of apicomplexan parasites. Int J Parasitol 39: 175-189.
  16. Cong W, Nie LB, Qin SY, Wang WL, Qian AD, Meng QF (2018) Prevalence of Neospora spp. in donkeys in China. Parasite 25, 16.
  17. Costa RC, Mesquita LP, Nunes MV, Oliveira IM, Oliveira LF, Souza AR, Maiorka PC, Varaschin MS (2018) Neospora caninum bioassay in gerbils using placental tissues from naturally infected goats. Vet Parasitol 249: 70-73.
  18. Dahourou LD, Gbati OB, Savadogo M, Yougbare B, Dicko A, Combari AH, Kamga-Waladjo AR (2019) Prevalence of Toxoplasma gondii and Neospora caninum infections in households sheep “Elevage en case” in Dakar, Senegal. Vet World 12: 1028-1032.
  19. Diakou A, Papadopoulos E, Panousis N, Karatzias C, Giadinis N (2013) Toxoplasma gondii and Neospora caninum seroprevalence in dairy sheep and goats mixed stock farming. Vet Parasitol 198: 387-390.
  20. Della Rosa P, Fiorentino MA, Morrell EL, Scioli MV, Paolicchi FA, Moore DP, Cantón GJ, Hecker YP (2021) Neospora caninum and Toxoplasma gondii as causes of reproductive losses in commercial sheep flocks from Argentina. Curr Res Parasitol Vector Borne Dis 1: 100057.
  21. Duarte PC, Conrad PA, Barr BC, Wilson WD, Ferraro GL, Packham AE, Carpenter TE, Gardner IA (2004) Risk of transplacental transmission of Sarcocystis neurona and Neospora hughesi in California horses. J Parasitol 90: 1345-1351.
  22. Dubey JP (2003) Review of Neospora caninum and neosporosis in animals. Korean J Parasitol 41: 1-16.
  23. Dubey JP, Buxton D, Wouda W (2006) Pathogenesis of Bovine Neosporosis. J Comp Pathol 134: 267-289.
  24. Dubey JP, Hemphill A, Calero-Bernal R, Schares G (2017) Neosporosis in animals, 1st ed., CRC Press, Taylor and Francis group.
  25. Dubey JP, Jenkins MC, Ferreira LR, Choudhary S, Verma SK, Kwok OC, Fetterer R, Butler E, Carstensen M (2014) Isolation of viable Neospora caninum from brains of wild gray wolves (Canis lupus). Vet Parasitol 201: 150-153.
  26. Dubey JP, Schares G (2011) Neosporosis in animals-the last five years. Vet Parasitol 180: 90-108.
  27. Dubey JP, Schares G, Ortega-Mora LM (2007) Epidemiology and control of neosporosis and Neospora caninum. Clin Microbiol Rev 20: 323-367.
  28. Faraj AA, Ghattof HH (2018) Diagnosis of Neospora caninum using ELIZA and study of histopathological changes in dairy goat in Wasit province: Iraq. J Entom Zool Stud 6: 1256-1259.
  29. Gazzonis AL, Garcia GA, Zanzani SA, Ortega Mora LM, Invernizzi A, Manfredi MT (2016) Neospora caninum infection in sheep and goats from north-eastern Italy and associated risk factors. Small Rumin Res 140: 7-12.
  30. Gennari SM, Pena HF, Lindsay DS, Lopes MG, Soares HS, Cabral AD, Vitaliano SN, Amaku M (2016) Prevalence of antibodies against Neospora spp. and Sarcocystis neurona in donkeys from northeastern Brazil. Rev Bras Parasitol Vet 25: 109-111.
  31. Gharekhani J, Yakhchali M, Berahmat R (2020) Neospora caninum infection in Iran (2004-2020): A review. J Parasit Dis 44: 671-686.
  32. Gharekhani J, Yakhchali M, Heidari R (2022) Molecular detection and phylogenetic analysis of Neospora caninum in various hosts from Iran. Comp Immunol Microbiol Infect Dis 80: 101737.
  33. Ghattof HH, Faraj AA (2015) Seroprevalence of Neospora caninum in goats in Wasit province Iraq. Int J Curr Microbiol Appl Sci 4: 182-191.
  34. Gondim LF (2006) Neospora caninum in wildlife. Trends Parasitol 22: 247-252.
  35. Gondim LF, McAllister MM (2022) Experimental Neospora caninum Infection in Pregnant Cattle: Different Outcomes Between Inoculation With Tachyzoites and Oocysts. Front Vet Sci 9: 911015.
  36. González-Warleta M, Castro-Hermida JA, Regidor-Cerrillo J, Benavides J, Álvarez-García G, Fuertes M, Ortega-Mora LM, Mezo M (2014) Neospora caninum infection as a cause of reproductive failure in a sheep flock. Vet Res 45: 88.
  37. Irehan B, Sonmez A, Atalay MM, Ekinci AI, Celik F, Durmus N, Ciftci AT, Simsek S (2022) Investigation of Toxoplasma gondii, Neospora caninum and Tritrichomonas foetus in abortions of cattle, sheep and goats in Turkey: Analysis by real-time PCR, conventional PCR and histopathological methods. Comp Immunol Microbiol Infect Dis 89: 101867.
  38. Japa O, Morand S, Karnchanabanthoeng A, Chaisiri K, Ribas A (2018) Detection of Neospora caninum (Toxoplasmatidae) in wild small mammals from Thailand. Folia Parasitologica 65.
  39. King JS, Jenkins DJ, Ellis JT, Fleming P, Windsor PA, Šlapeta J (2011) Implications of wild dog ecology on the sylvatic and domestic life cycle of Neospora caninum in Australia. Vet J 188: 24-33.
  40. Langoni H, Greca HJ, Guimarães FF, Ullmann LS, Gaio FC, Uehara RS, Rosa EP, Amorim RM, Da Silva RC (2011) Serological profile of Toxoplasma gondii and Neospora caninum infection in commercial sheep from São Paulo State, Brazil. Vet Parasitol 177: 50-54.
  41. Locatelli-Dittrich R, Dittrich JR, Richartz RR, Gasino JM, Antunes J, Pinckney RD, Deconto I, Hoffmann DC, Thomaz-Soccol V (2006) Investigation of Neospora sp. and Toxoplasma gondii antibodies in mares and in precolostral foals from Parana State, Southern Brazil. Vet Parasitol 135: 215-221.
  42. Machačová T, Bártová E, Di Loria A, Sedlák K, Guccione J, Fulgione D, Veneziano V (2013) Seroprevalence and risk factors of Neospora spp. in donkeys from Southern Italy. Vet Parasitol 198: 201-204.
  43. Manca R, Ciccarese G, Scaltrito D, Chirizzi D (2022) Detection of Anti-Neospora caninum Antibodies on Dairy Cattle Farms in Southern Italy. Vet Sci 9: 87
  44. Marsh AE, Barr BC, Packham AE, Conrad PA (1998) Description of a new neospora species (Protozoa: apicomplexa: sarcocystidae). J Parasitol 5: 84-91.
  45. Mazuz ML, Mimoun L, Schvartz G, Tirosh-Levy S, Savitzki I, Edery N, Blum SE, Baneth G, Pusterla N, Steinman A (2020) Detection of Neospora caninum infection in aborted equine fetuses in Israel. Pathogenes 9: 1-11.
  46. Mendoza-Morales LF, Lagorio V, Corigliano MG, Sánchez-López E, Ramos-Duarte VA, Clemente M, Sander VA (2022) Neosporosis in sheep: A systematic review and meta-analysis of global seroprevalence and related risk factors. Acta Trop 233: 106569.
  47. Moore DP, de Yaniz MG, Odeón AC, Cano D, Leunda MR, Späth EA, Campero CM (2007) Serological evidence of Neospora caninum infections in goats from La Rioja Province, Argentina. Small Rumin Res 73: 256-258.
  48. Moreira TR, Sarturi C, Stelmachtchuk FN, Andersson E, Norlander E, de Oliveira FL, Machado Portela J, Marcili A, Emanuelson U, Gennari SM, Minervino AH (2019) Prevalence of antibodies against Toxoplasma gondii and Neospora spp. in equids of Western Pará Brazil. Acta Trop 189: 39-45.
  49. Moreno B, Collantes-Fernández E, Villa A, Navarro A, Regidor-Cerrillo J, Ortega-Mora LM (2012) Occurrence of Neospora caninum and Toxoplasma gondii infections in ovine and caprine abortions. Vet Parasitol 187: 312-318.
  50. Müller N, Zimmermann V, Hentrich B, Gottstein B (1996) Diagnosis of Neospora caninum and Toxoplasma gondii infection by PCR and DNA hybridization immunoassay. J Clin Microbiol 34: 2850-2852.
  51. Nayeri T, Sarvi S, Moosazadeh M, Daryani A (2022) The Global Prevalence of Neospora caninum Infection in Sheep and Goats That Had an Abortion and Aborted Fetuses: A Systematic Review and Meta-Analysis. Front Vet Sci 9: 870904
  52. Nooruldeen MY, Jaafar SE, Salih AI (2021) Seroprevalence of Neospora caninum infections in cattle in Kirkuk province. Iraqi J Vet Sci 35: 331-334.
  53. Novoa MB, Soler JP, Cirone KM, Hecker YP, Valentini BS, Primo ME, Moore DP (2023) Use and comparison of serologic assays to detect anti-Neospora caninum antibodies in farmed red deer (Cervus elaphus). Vet Parasitol 313: 109839.
  54. Rahmani SS, Malekifard F, Tavassoli M (2022) Neospora caninum, a cause of abortion in donkeys (Equus asinus) in Iran. Parasitol Res 121: 367-372.
  55. Reichel MP, Ayanegui-Alcérreca MA, Gondim LF, Ellis JT (2013) What is the global economic impact of Neospora caninum in cattle - the billion dollar question. Int J Parasitol 43: 133-142.
  56. Rodrigues AA, Brito DR, Kono IS, Reis SS, de Souza Lima Nino B, Nascimento TV, Barros LD, Garcia JL, de Cunha IA (2022) Seroprevalence of Neospora caninum and risk factors associated with infection in water buffaloes (Bubalus bubalis) from Maranhão State, Brazil. Vet Parasitol Reg Stud Reports 27: 100661.
  57. Sedlák K, Bartova E, Machacova T (2014) Seroprevalence of Neospora caninum in cats from the Czech Republic. Acta Parasitol 59: 359-361.
  58. Špilovská S, Reiterová K (2008) Seroprevalence of Neospora caninum in aborting sheep and goats in the Eastern Slovakia. Folia Vet 52: 33-35.
  59. Tayyub M, Ali S, Javid A, Imran M (2022) Molecular detection of Toxoplasma gondii and Neospora caninum in rock pigeons (Columba livia) in Punjab, Pakistan. Parasitol Res 121: 1499-1505
  60. Tirosh-Levy S, Savitsky I, Blinder E, Mazuz ML (2022) The involvement of protozoan parasites in sheep abortions – a ten-year review of diagnostic results. Vet Parasitol 303: 109664.
  61. Tirosh-Levy S, Steinman A, Minderigiu A, Arieli O, Savitski I, Fleiderovitz L, Edery N, Schvartz G, Mazuz ML (2020) High Exposure to Toxoplasma gondii and Neospora Spp. in Donkeys in Israel: Serological Survey and Case Reports. Animals 10: 1921
  62. Waap H, de Oliveira UV, Nunes T, Gomes J, Gomes T, Bärwald A, Dias Munhoz A, Schares G (2020) Serological survey of Neospora spp. and Besnoitia spp. in horses in Portugal. Vet Parasitol Reg Stud Reports 20: 100391.
  63. Wouda W, van den Ingh TS, van Knapen F, Sluyter FJ, Koeman JP, Dubey JP (1992) Neospora abortion in cattle in The Netherlands. Tijdschr Diergeneeskd 117: 599-602.
  64. Yang J, Ai J, Qi T, Ni X, Xu Z, Guo L, Sun Y, Li Y, Kang M, Li J (2022) Toxoplasma gondii and Neospora caninum Infections in Stray Cats and Dogs in the Qinghai-Tibetan Plateau Area, China. Animals 12: 1390
  65. Zhao SS, Tao DL, Chen JM, Chen X, Geng XL, Wang JW, Yang X, Song JK, Liu Q, Zhao GH (2022) Neospora caninum infection activated autophagy of caprine endometrial epithelial cells via mTOR signaling. Vet Parasitol 304: 109685.
Go to article

Authors and Affiliations

R.R. Mohammed
1
M. Tavassoli
1
K.R. Sidiq
2
B. Esmaeilnejad
1

  1. Department of Pathobiology, Faculty of Veterinary Medicine, Urmia University, Nazloo Campus, PO Box 1177, Urmia, West Azerbaijan, Iran
  2. Department of Medical Laboratory Science, College of Medical and Applied Sciences, Charmo University, 46023 Chamchamal, Sulaimani, Kurdistan Region, Iraq
Download PDF Download RIS Download Bibtex

Abstract

Respiratory diseases constitute a major health problem in small ruminant herds around the world, and parainfluenza virus type 3 (PIV-3) has been shown to play a vital role in their etiology. This cross-sectional study describes the serological status of the non-vaccinated dairy goat popu- lation in Poland with respect to PIV-3 infection and investigates the relationship between the presence of antibodies to PIV-3 and some basic herd-level and animal-level factors, including small ruminant lentivirus (SRLV) infection. Serum samples from 1188 goats from 48 herds were tested for the concentration of antibodies to PIV-3 using a quantitative immunoenzymatic assay. Specific antibodies were detected in all tested goats from all herds. The concentration of PIV-3 antibodies varied from 8.4 to >240 ng/ml (median 95.9 ng/ml) and was significantly higher in goats from larger herds and from these herds in which cough was often observed by farmers. Moreover, it was noted that female goats had higher antibody concentrations than males. On the other hand, the concentration of PIV-3 antibodies did not prove to be significantly linked to the presence of SRLV infection. This study shows that PIV-3 infection in the Polish goat population is widespread and appears to contribute to the occurrence of respiratory diseases in goat herds.
Go to article

Authors and Affiliations

A. Moroz
1
M. Czopowicz
1
M. Mickiewicz
1
L. Witkowski
1
O. Szaluś-Jordanow
2
T. Nalbert
1
M.D. Klimowicz-Bodys
3
I. Markowska-Daniel
1
E. Bagnicka
4
J. Kaba
1

  1. Division of Veterinary Epidemiology and Economics, Institute of Veterinary Medicine, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159c, 02-776 Warsaw, Poland
  2. Department of Small Animal Diseases with Clinic, Institute of Veterinary Medicine,Warsaw University of Life Sciences-SGGW, Nowoursynowska 159c, 02-776 Warsaw, Poland
  3. Division of Infectious Diseases of Animals and Veterinary Administration,Department of Epizootiology and Clinic of Birds and Exotic Animals, Faculty of Veterinary Medicine, Wroclaw University of Environmental and Life Sciences, pl. Grunwaldzki 45, 50-366 Wroclaw, Poland
  4. Institute of Genetics and Animal Biotechnology,Polish Academy of Sciences, Postępu 36A, Jastrzębiec, 05-552 Magdalenka, Poland

This page uses 'cookies'. Learn more