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		<title>BMC Veterinary Research - Latest articles</title>
		<link>http://www.biomedcentral.com/bmcvetres/</link>
		<description>The latest articles from BMC Veterinary Research (ISSN 1746-6148) published by 
				
				BioMed Central
		</description>
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				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/16"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/15"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/14"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/13"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/12"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/11"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/10"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/9"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/8"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1746-6148/4/7"/>			    
            
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		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/16">
            
            <title>Pruritus is a common feature in sheep infected with the BSE agent</title>
			<description>Background:
The variability in the clinical or pathological presentation of transmissible spongiform encephalopathies (TSEs) in sheep, such as scrapie and bovine spongiform encephalopathy (BSE), has been attributed to prion protein genotype, strain, breed, clinical duration, dose, route and type of inoculum and the age at infection. The study aimed to describe the clinical signs in sheep infected with the BSE agent throughout its clinical course to determine whether the clinical signs were as variable as described for classical scrapie in sheep. The clinical signs were compared to BSE-negative sheep to assess if disease-specific clinical markers exist.
Results:
Forty-seven (34%) of 139 sheep, which comprised 123 challenged sheep and 16 undosed controls, were positive for BSE. Affected sheep belonged to five different breeds and three different genotypes (ARQ/ARQ, VRQ/VRQ and AHQ/AHQ). None of the controls or BSE exposed sheep with ARR alleles were positive. Pruritus was present in 41 (87%) BSE positive sheep; the remaining six were judged to be pre-clinically infected. Testing of the response to scratching along the dorsum of a sheep proved to be a good indicator of clinical disease with a test sensitivity of 85% and specificity of 98% and usually coincided with weight loss. Clinical signs that were displayed significantly earlier in BSE positive cases compared to negative cases were behavioural changes, pruritic behaviour, a positive scratch test, alopecia, skin lesions, teeth grinding, tremor, ataxia, loss of weight and loss of body condition. The frequency and severity of each specific clinical sign usually increased with the progression of disease over a period of 16-20 weeks.
Conclusions:
Our results suggest that BSE in sheep presents with relatively uniform clinical signs, with pruritus of increased severity and abnormalities in behaviour or movement as the disease progressed. Based on the studied sheep, these clinical features appear to be independent of breed, affected genotype, dose, route of inoculation and whether BSE was passed into sheep from cattle or from other sheep, suggesting that the clinical phenotype of BSE is influenced by the TSE strain more than by other factors. The clinical phenotype of BSE in the genotypes and breed studied was indistinguishable from that described for classical scrapie cases.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/16</link>
			
			 	<dc:creator>Timm Konold, Gemma Bone, Alberto Vidal-Diez, Raul Tortosa, Andrew Davis, Glenda Dexter, Peter Hill, Martin Jeffrey, Marion M Simmons, Melanie J Chaplin, Susan J Bellworthy and Christine Berthelin-Baker</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:16</dc:source>
			<dc:date>2008-04-29</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-16</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>16</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-04-29</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/15">
            
            <title>Cross-sectional prospective survey to study indication-based usage of antimicrobials in animals: Results of use in cattle</title>
			<description>Background:
Indication-based data on the use of antimicrobials in animals were collected using a prospective cross-sectional survey, similarly as for surveys carried out in human medicine, but adapting the questionnaire to include veterinary-specific issues. The participating veterinarians were randomly selected from a sample population of practising veterinarians. The sampling was stratified to take into account the proportions of different types of veterinary practice in the country. All patients consulting the veterinary practice during a 1-week period were included in the study and veterinarians returned a completed questionnaire for each patient receiving antimicrobial treatment. As cattle received most of the treatments, results from the survey are given using cattle as an example species.
Results:
The survey was sent to 681 veterinarians, of whom 262 (39%) responded. In total 2850 questionnaires were completed. The largest quantities of antimicrobials, measured in kilograms, were used for cattle, followed by pigs, dogs and horses. The species that were treated most were cattle (n = 1308), dogs (n = 989) and cats (n = 311). For cattle, the most common reason for treatment was acute mastitis (52%), followed by dry-cow therapy (21%), subclinical mastitis (6%) and treatment for acute enteritis (4%). The remaining treatments covered 17% of cattle patients and 15 different indications. For acute mastitis, parenteral or intramammary treatment was used in 36% and 34% of the cases, respectively. The remaining 30% received both treatments simultaneously. Of the parenteral treatments (n = 459), benzyl penicillin was used in 83% of the treated animals (n = 379), while fluoroquinolones were used in 49 cases (11%). Of the 433 cows receiving intramammary treatment, ampicillin combined with cloxacillin was most commonly used (n = 157; 36%), followed by cephalexin+streptomycin (n = 113; 26%).
Conclusion:
This cross-sectional prospective survey provided a useful method for the collection of information on the indication-based use of antimicrobials in different animal species. Cattle were the most commonly treated animal species during the study period. The most common indication for antimicrobial use in cows was mastitis. Benzyl penicillin was the drug most frequently used for the treatment of mastitis, which seems appropriate according to the national guidelines on the use of antimicrobials in cattle in Finland.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/15</link>
			
			 	<dc:creator>Katariina Thomson, Merja Rantala, Maria Hautala, Satu Py&#246;r&#228;l&#228; and Liisa Kaartinen</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:15</dc:source>
			<dc:date>2008-04-14</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-15</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>15</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-04-14</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/14">
            
            <title>Evidence of scrapie transmission via milk</title>
			<description>Background:
The risk of scrapie infection increases with increased duration and proximity of contact between sheep at lambing. Scrapie infectivity has not been detected in milk but cellular prion protein, the precursor of disease-associated prion protein PrPd, has been found in milk from ruminants. To determine whether milk is able to transmit scrapie, 18 lambs with a prion protein genotype associated with high susceptibility to scrapie (VRQ/VRQ) were fed milk from twelve scrapie-affected ewes of the same genotype, and 15 VRQ/VRQ sheep reared on scrapie-free dams served as controls.
Results:
Three lambs fed milk from scrapie-affected ewes were culled due to intercurrent diseases at 43, 44 and 105 days of age respectively, and PrPd was detected in the distal ileum of the first two lambs, whilst PrPd was not found in lymphoreticular tissues in the third lamb. A control lamb, housed in a separate pen and culled at 38 days of age, was also negative for PrPd in a range of tissues. Samples of recto-anal mucosa associated lymphoid tissue collected from the remaining 15 live lambs at seven months of age (between five to seven months after mixing) were positive for PrPd in the scrapie milk recipients, whereas PrPd was not detected in the remaining 14 controls at that time. A subsequent sample collected from control lambs revealed PrPd accumulation in two of five lambs eight months after mixing with scrapie milk recipients suggestive of an early stage of infection via lateral transmission. By contrast, the control sheep housed in the same building but not mixed with the scrapie milk recipients were still negative for PrPd.
Conclusion:
The presence of PrPd in distal ileum and rectal mucosa indicates transmission of scrapie from ewe to lamb via milk (or colostrum) although it is not yet clear if such cases would go on to develop clinical disease. The high level of infection in scrapie-milk recipients revealed by rectal mucosal testing at approximately seven months of age may be enhanced or supplemented by intra-recipient infection as these lambs were mixed together after feeding with milk from scrapie-affected ewes and we also observed lateral transmission from these animals to lambs weaned from scrapie-free ewes.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/14</link>
			
			 	<dc:creator>Timm Konold, S Jo Moore, Susan J Bellworthy and Hugh A Simmons</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:14</dc:source>
			<dc:date>2008-04-08</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-14</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>14</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-04-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/13">
            
            <title>No temporal trends in the prevalence of atypical scrapie in British sheep, 2002-2006</title>
			<description>Background:
So-called atypical scrapie was first identified in Great Britain (GB) in 2002 following the introduction of wide-scale scrapie surveillance. In particular, abattoir and fallen stock surveys have been carried out in GB since 2002, with a total of 147 atypical positives identified by the end of 2006. The results of these surveys provide data with which to assess temporal trends in the prevalence of atypical scrapie in sheep in Great Britain between 2002 and 2006.
Results:
Using the results of abattoir and fallen stock surveys, the prevalence of atypical scrapie (percentage of samples positive) was estimated. The prevalence in the abattoir and fallen stock surveys, for all years combined, was 0.09% (95% confidence interval (CI): 0.08%-0.11%) and 0.07% (95% CI: 0.05%-0.11%), respectively. There were no significant temporal trends in either survey. Comparing the surveys' results, there were no significant differences in annual prevalence or the prevalence within PrP genotypes. For the abattoir survey, the PrP genotype with the highest prevalence was AHQ/AHQ, which was significantly higher than all other genotypes, except ARR/AHQ, AHQ/ARH and ARH/ARQ.
Conclusions:
The estimated prevalence of atypical scrapie was similar in both the abattoir and fallen stock surveys. Our results indicate there was no significant temporal trend in prevalence, adding to evidence that this atypical form of scrapie may be a sporadic condition or, if it is infectious, that the force of infection is very low. </description>
			<link>http://www.biomedcentral.com/1746-6148/4/13</link>
			
			 	<dc:creator>K. Marie McIntyre, Victor J del Rio Vilas and Simon Gubbins</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:13</dc:source>
			<dc:date>2008-04-02</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-13</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>13</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-04-02</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/12">
            
            <title>Identification of differentially expressed genes in ileal Peyer's Patch of scrapie-infected sheep using RNA arbitrarily primed PCR</title>
			<description>BackgoundIn scrapie and prion diseases, the knowledge concerning genes involved in host response during the early infection period in the lymphoid tissues, still remains limited. In the present study, we have examined differential gene expression in ileal Peyer's patches and in laser microdissected follicles of sheep infected with scrapie.
Methods:
Ileal Peyer's patches and laser microdissected follicles were of scrapie and control lambs with susceptible genotypes for classical scrapie. Potential regulated genes were found using RNA arbitrarily primed polymerase chain reaction (RAP-PCR) and fingerprinting. The differentially expressed genes were confirmed using real-time RT-PCR.
Results:
The expression of three genes (MAPRE3, LOC729073 and DNAJC3), were found to be significantly altered in scrapie infected lambs (P &lt; 0.05).
Conclusion:
The three genes have not previously been associated with prion diseases and are interesting as they may reflect biological processes involved in the molecular pathogenesis of prion diseases.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/12</link>
			
			 	<dc:creator>Lars Austb&#248;, Andreas Kampmann, Ulf M&#252;ller-Ladner, Elena Neumann, Ingrid Olsaker and Grethe Skretting</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:12</dc:source>
			<dc:date>2008-03-28</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-12</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>12</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-28</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/11">
            
            <title>Construction of networks with intrinsic temporal structure from UK cattle movement data</title>
			<description>Background:
The implementation of national systems for recording the movements of cattle between agricultural holdings in the UK has enabled the development and parameterisation of network-based models for disease spread. These data can be used to form a network in which each cattle-holding location is represented by a single node and links between nodes are formed if there is a movement of cattle between them in the time period selected. However, this approach loses information on the time sequence of events thus reducing the accuracy of model predictions. In this paper, we propose an alternative way of structuring the data which retains information on the sequence of events but which still enables analysis of the structure of the network. The fundamental feature of this network is that nodes are not individual cattle-holding locations but are instead direct movements between pairs of locations. Links are made between nodes when the second node is a subsequent movement from the location that received the first movement.
Results:
Two networks are constructed assuming (i) a 7-day and (ii) a 14-day infectious period using British Cattle Movement Service (BCMS) data from 2004 and 2005. During this time period there were 4,183,670 movements that could be derived from the database. In both networks over 98% of the connected nodes formed a single giant weak component. Degree distributions show scale-free behaviour over a limited range only, due to the heterogeneity of locations: farms, markets, shows, abattoirs. Simulation of the spread of disease across the networks demonstrates that this approach to restructuring the data enables efficient comparison of the impact of transmission rates on disease spread.
Conclusion:
The redefinition of what constitutes a node has provided a means to simulate disease spread using all the information available in the BCMS database whilst providing a network that can be described analytically. This will enable the construction of generic networks with similar properties with which to assess the impact of small changes in  network structure on disease dynamics.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/11</link>
			
			 	<dc:creator>M Fred Heath, Matthew C Vernon and Cerian R Webb</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:11</dc:source>
			<dc:date>2008-03-20</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-11</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>11</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-20</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/10">
            
            <title>Progressive Retinal Atrophy in the Border Collie: A new XLPRA</title>
			<description>Background:
Several forms of progressive retinal atrophy (PRA) segregate in more than 100 breeds of dog with each PRA segregating in one or a few breeds. This breed specificity may be accounted for by founder effects and genetic drift, which have reduced the genetic heterogeneity of each breed, thereby facilitating the identification of causal mutations. We report here a new form of PRA segregating in the Border Collie breed. The clinical signs, including the loss of night vision and a progressive loss of day vision, resulting in complete blindness, occur at the age of three to four years and may be detected earlier through systematic ocular fundus examination and electroretinography (ERG).
Results:
Ophthalmic examinations performed on 487 dogs showed that affected dogs present a classical form of PRA. Of those, 274 have been sampled for DNA extraction and 87 could be connected through a large pedigree. Segregation analysis suggested an X-linked mode of transmission; therefore both XLPRA1 and XLPRA2 mutations were excluded through the genetic tests.
Conclusion:
Having excluded these mutations, we suggest that this PRA segregating in Border Collie is a new XLPRA (XLPRA3) and propose it as a potential model for the homologous human disease, X-Linked Retinitis Pigmentosa.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/10</link>
			
			 	<dc:creator>Thierry Vilboux, Gilles Chaudieu, Patricia Jeannin, Delphine Delattre, Benoit Hedan, Catherine Bourgain, Guillaume Queney, Francis Galibert, Anne Thomas and Catherine Andr&#233;</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:10</dc:source>
			<dc:date>2008-03-03</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-10</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>10</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-03</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/9">
            
            <title>Local spread of classical swine fever upon virus introduction into The Netherlands: Mapping of areas at high risk</title>
			<description>Background:
In the recent past, the introduction of Classical Swine Fever Virus (CSFV) followed by between-herd spread has given rise to a number of large epidemics in The Netherlands and Belgium. Both these countries are pork-exporting countries. Particularly important in these epidemics has been the occurrence of substantial "neighborhood transmission" from herd to herd in the presence of base-line control measures prescribed by EU legislation. Here we propose a calculation procedure to map out "high-risk areas" for local between-herd spread of CSFV as a tool to support decision making on prevention and control of CSFV outbreaks. In this procedure the identification of such areas is based on an estimated inter-herd distance dependent probability of neighborhood transmission or "local transmission". Using this distance-dependent probability, we derive a threshold value for the local density of herds. In areas with local herd density above threshold, local transmission alone can already lead to epidemic spread, whereas in below-threshold areas this is not the case. The first type of area is termed 'high-risk' for spread of CSFV, while the latter type is termed 'low-risk'.
Results:
As we show for the case of The Netherlands, once the distance-dependent probability of local transmission has been estimated from CSFV outbreak data, it is possible to produce a map of the country in which areas of high-risk herds and of low-risk herds are identified. We made these maps even more informative by estimating border zones between the two types of areas. In these border zones the risk of local transmission of infection to a nearby high-risk area exceeds a certain level.
Conclusion:
The risk maps provide an easily understandable visualization of the spatial heterogeneities in transmission risk. They serve as a tool for area-specific designs of control strategies, and possibly also for spatial planning of areas where livestock farming is allowed. Similar risk maps can in principle be constructed for other highly-transmissible livestock infections that spread via neighborhood transmission.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/9</link>
			
			 	<dc:creator>Gert Jan Boender, Gonnie Nodelijk, Thomas J Hagenaars, Armin RW Elbers and Mart CM de Jong</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:9</dc:source>
			<dc:date>2008-02-25</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-9</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>9</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-02-25</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/8">
            
            <title>Epithelial expression of mRNA and protein for IL-6, IL-10 and TNF-&#945; in endobronchial biopsies in horses with recurrent airway obstruction</title>
			<description>Background:
The aim of this study was to evaluate the contribution of bronchial epithelium to airway inflammation, with focus on mRNA and protein expression of cytokines of innate immunity IL-6, IL-10 and TNF-&#945;, in horses with Recurrent Airway Obstruction (RAO) during exacerbation and in remission.
Results:
Despite marked clinical and physiologic alterations between exacerbation and after remission in the RAO horses no differences were detected in either cytokine mRNA or protein levels. Moreover, the expression of investigated cytokines in RAO horses on pasture did not differ from controls.In comparing real-time PCR analysis to results of immunohistochemistry only IL-10 mRNA and protein levels in RAO horses on pasture were significantly correlated (rs = 0.893, p = 0.007). Curiously, in controls examined on pasture the TNF-&#945; protein level was positively correlated to IL-10 mRNA expression (rs = 0.967, p = 0.007) and negatively correlated to IL-6 mRNA expression (rs = -0.971, p = 0.001).
Conclusion:
Given the complementary relationship of assessing cytokines directly by immunohistochemistry, or indirectly by PCR to mRNA, the lack of significant changes in either mRNA or protein levels of IL-6, IL-10 or TNF-&#945; mRNA in RAO horses in exacerbation suggests that these particular cytokines in bronchial tissue may not play a substantive role in the active inflammation of this disease. To support this contention further studies examining time dependency of expression of IL-6, IL-10 or TNF-&#945; are needed, as is expansion of the range of cytokines to include other key regulators of airway inflammation.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/8</link>
			
			 	<dc:creator>Miia Riihim&#228;ki, Amanda Raine, Jamshid Pourazar, Thomas Sandstr&#246;m, Tatiana Art, Pierre Lekeux, Laurent Cou&#235;til and John Pringle</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:8</dc:source>
			<dc:date>2008-02-23</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-8</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>8</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-02-23</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1746-6148/4/7">
            
            <title>Trypanosomosis in The Gambia: prevalence in working horses and donkeys detected by whole genome amplification and PCR, and evidence for interactions between trypanosome species</title>
			<description>Background:
The Gambia has an increasing population of equidae largely used for agriculture and transportation. A review of cases at The Gambian Horse and Donkey Trust (GHDT) indicated that a common reason for presentation is a poorly defined medical condition often attributed to trypanosomosis. There are few reports describing the prevalence or the range of clinical signs associated with infection with different species of trypanosomes in horses and donkeys, but given the importance of these animals, the role of trypanosomosis requires investigation.
Results:
In total 241 animals from the Central River Division in The Gambia (183 horses and 58 donkeys) were screened using Whole Genome Amplification (WGA) followed by trypanosome species identification using polymerase chain reaction (PCR). The results indicated overall trypanosome prevalence of 91%; with an infection rate of 31% for Trypanosoma congolense Savannah, 87% for Trypanosoma vivax and 18% for Trypanosoma brucei sp. Multiple species were present in 43% of infections. Microscopy had a good specificity (100%) and positive predictive value (100%) for trypanosome detection, but the sensitivity (20%) and negative predictive value (10.5%) were low relative to PCR-based diagnosis.Infection with T congolense showed the greatest negative effect on packed cell volume (PCV), while infection with T. brucei sp also had a significant, although lesser, negative effect on PCV. In addition, cases positive by microscopy were associated with significantly lower PCV. However, concurrent infection with T. vivax appeared to cause less effect on PCV, compared to animals infected with T. congolense alone.
Conclusion:
The prevalence of Trypanosomosis was high in both horses and donkeys. Infection with T. congolense appeared to have the greatest clinical significance, while T. vivax infection may be of limited clinical significance in this population. Indeed, there is evidence of T. vivax co-infection ameliorating the pathology caused by T. congolense. WGA and PCR allowed a more comprehensive analysis of field infections with the detection of infections below the threshold of microscopy, and provided indications of interactions between parasite species that would otherwise remain undetected. The study raises important questions about the epidemiology of trypanosome infection in relation to disease that require a full scale longitudinal analysis.</description>
			<link>http://www.biomedcentral.com/1746-6148/4/7</link>
			
			 	<dc:creator>Gina L Pinchbeck, Liam J Morrison, Andy Tait, Joanna Langford, Lucinda Meehan, Saloum Jallow, Jibril Jallow, Amadou Jallow and Robert M Christley</dc:creator>
			
			<dc:source>BMC Veterinary Research 2008, 4:7</dc:source>
			<dc:date>2008-02-20</dc:date>
			<dc:identifier>doi:10.1186/1746-6148-4-7</dc:identifier>
			
			
							
					<prism:publicationName>BMC Veterinary Research</prism:publicationName>
					
			
							
					<prism:issn>1746-6148</prism:issn>
					
			
							
					<prism:volume>4</prism:volume>
					
			
							
					<prism:startingPage>7</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-02-20</prism:publicationDate>
					

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