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SCIENTIFUR SCIENTIFIC INFORMATION IN FUR ANIMAL PRODUCTION Vol. 35, No. 2 INTERNATIONAL FUR ANIMAL SCIENTIFIC ASSOCIATION

SCIENTIFUR - scientific information in Fur Animal Production. SCIENTIFUR scientific information for those involved in fur animal production is published by the International Fur Animal Scientific Association (IFASA). SCIENTIFUR is the contact link between fur animal researchers all over the world and serves as an outlet for scientific and other communication between researchers and others who are interested in the production of fur bearing animals. As such SCIENTIFUR contains reports of scientific and applied nature as well as abstracts of information published elsewhere and information regarding congresses, scientific meetings etc. SCIENTIFUR is published as four issues per year (one volume). REVIEWED SCIENTIFIC ARTICLES. Papers received for publication as Reviewed Scientific Articles will be sent for scientific approval by peer review. SHORT COMMUNICATIONS. Other original papers can be published in SCIENTIFUR as short communications. In regard to such articles the author(s) alone is (are) responsible for the scientific validity of the article. Such papers must not exceed 4 printed pages. EDITOR S ADDRESS. All kinds of material suited for publication or abstracting in SCIENTIFUR have to be forwarded to the Editor: Vivi Hunnicke Nielsen Tel: +45 8999 1361 SCIENTIFUR Fax: +45 8999 1300 P.O. Box 14 DK-8830 Tjele, Denmark E-mail: Scientifur@agrsci.dk SUBSCRIPTION: DKK 650.- per volume (year) including bank charges and postage. Please note that members can subscribe, for personal use only, at a reduced rate. Please apply for membership and further details at http://www.ifasanet.org or to the IFASA treasurer. TRESURER S ADDRESS. All correspondence regarding subscription and payment should be addressed to the Treasurer: Steen H. Møller Tel: +45 8999 1346 IFASA Fax: +45 8999 1500 P.O. Box 14 DK-8830 Tjele, Denmark E-mail: IFASA@agrsci.dk INDEXING: Titles that have been published in SCIENTIFUR are covered in an electronic SCIENTIFUR INDEX. Regional Scientifur Representatives Canada: Dr. Bruce Hunter: E-mail: bhunter@ovc.uoguelph.ca USA: Dr. Jack Rose: E-mail: rosewill@isu.edu Finland: M.Sc. Nita Koskinen: E-mail: nita.koskinen@mtt.fi Iceland: Advisor Einar Einarsson: E-mail: einare@krokur.is Norway: Veterinary advisor Gorm Sanson: E-mail: sanson@norpels.no The Netherlands: Ing. Jan derond: E-mail: info@edelveen.com Poland: Dr. Malgorzata Sulik: E-mail: m.sulik@biot.ar.szczecin.pl International Fur Animal Scientific Association (IFASA). Board of directors: Dr. Steen H. Møller (President, Treasurer): E-mail: IFASA@agrsci.dk Dr. Bruce D. Murphy (Past President): E-mail: murphyb@medvet.umontreal.ca Dr. Kirsti Rouvinen-Watt (Vice President): E-mail: krouvinen@nsac.ca Mr. Knud J. Vest. E-mail: kjv@kopenhagenfur.com Dr. Gorm Sanson. E-mail: sanson@norpels.no Dr. Marian Brzozowski. E-mail: brzozowskim@delta.sggw.waw.pl

Notes 15 Notes from the Editor This volume of Scientifur presents the preliminary program for the Xth International Scientific Congress in Fur animal Production. The IFASA Congress will be held in Copenhagen in Denmark, August 21-24,2012. Efficient use of feed is important in fur animal production. Feed expenses make up a considerable part of production costs and inefficient use of feedstuff causes undesirable discharge of nutrients to the environment. Abstracts are presented with suggestion of dietary protein content and selection conditions, respectively which improve feed utilization. Welfare is constantly in focus. The relationship between stress and stereotypic behaviour is reported in another abstract. An abstract demonstrates that mink homozygous for the Aleutian allele show the characteristic formation of abnormally large granules in leukocytes. Furthermore, a new differential diagnostic test is presented that identify the vaccine and fields strains of Canine distemper virus. Another study shows that mink coronavirus possess high genomic variability. Vivi Hunnicke Nielsen Editor Scientifur

16 Scientifur, Vol. 35 No. 3, 2011

Preliminary program Tuesday August 21 09.00 13.30 Arrival, registration at Copenhagen Scandic 13.30 22.00 Pre-congress event at Kopenhagen Fur Wednesday August 22 Morning Opening Ceremony Welcome by Chairman of the Danish Fur Breeders Association / CEO Speech by the Danish Agricultural Minister Speech by the president of IFASA guest speaker Plenary/parallel: Health & Disease moderator: Tove Clausen & Anne Sofie Hammer 12.30 13.30 Lunch Afternoon excursion to Kronborg/Frederiksborg/Amalienborg Castle membership meeting and election Thursday August 23 Morning Plenary/parallel: Nutrition, Feeding, & Management moderator: Jan Elnif & Tor Michael Lassen 12.00 13.00 Lunch Afternoon Plenary/parallel: Breeding, Genetics, & Reproduction moderator: Vivi Hunniche Nielsen & Anne-Helene Tauson Coffee break Plenary/parallel: Theme on WelFur for mink and foxes moderator: Steen H. Møller & Jakko Mononen Poster session 19.00 Gala Dinner Friday August 24 Morning Plenary/parallel: Behaviour & Welfare moderator: Leif Lau Jeppesen & Steffen W. Hansen Closing Ceremony best oral presentation and best poster 12.30 13.30 Lunch Plenaries and sessions will be oral presentations. Special focus themes: Within the program, we aim to dedicate two to three sessions to pre-defined focus themes, such as: Aleutian disease, N-reduction or Limits to body size and condition. Different aspects of these themes will be approached through presentations from different disciplines such as health, disease, nutrition, feeding, breeding, genetics, behavior, welfare, management & ethics. Organizing committee: Peter Foged Larsen, Chairman (Kopenhagen Fur) Trine Storm (Kopenhagen Fur) Pernille Schack (Kopenhagen Fur) Jesper Clausen (Kopenhagen Fur) Leif Bruun (Kopenhagen Fur) Scientific Commitee: Tove Clausen (Kopenhagen Fur) Anne Sofie Hammer (Technical University of Denmark) Jan Elnif (University of Copenhagen) Vivi Hunniche Nielsen (University of Aarhus) Steffen W. Hansen (University of Aarhus) Steen H. Møller (University of Aarhus) Peter Foged Larsen (Kopenhagen Fur)

Abstracts. 19 Effects of diets with different protein and dlmethionine levels on the growth performance and N-balance of growing minks H. Zhang, G.Y. Li, E.J. Ren, X.M Xing, Q Wu, F.H. Yang This study was performed to evaluate the effects of diets with different protein and dl-methionine (Met) levels on nitrogen (N) retention, nutrient digestibility, growth performance, and some blood parameters in growing minks. Eighty healthy male minks were selected and randomly divided into five groups with different types of diet. The dietary protein levels, expressed as percentage of dry matter (DM), were 36% (HP) and 28% (LP), corresponding to average 363g and 295g protein/kg DM, respectively. LP was supplemented with Met (0.3%, 0.6% and 0.9% DM); the codes were LP+M1, LP+M2 and LP+M3, respectively. From July to middle of September, the average daily gain and feed: gain ratio (F/G) of the minks that received the diet with 0.6% Met added to the low protein diet was better than feeding HP and other groups. Fecal N and Urinary N of group LP+M2 were the lowest one, in contrast, the daily retention of N was the highest one. Digestibility of DM and CP were not affected by different diets, but digestibility of fat declined with dietary protein level decreasing. Serum urea nitrogen (SUN) was affected by different protein and Met levels. Considering all factors the best performance could be observed offering LP+M2, the prime level of Met was 13.87 g/kg DM in dietary, and 258.5 g digestible protein kg(-1) DM was enough for mink in growing period. Furthermore, addition of Met in low protein diets for minks would be beneficial in terms of reduced feed expenses and lower nitrogen emissions to the environment. J Anim Physiol Anim Nutr (Berl), 2011: Jun 3. doi: 10.1111/j.1439-0396.2011.01160.x. [Epub ahead of print] Response to selection and genotype-environment interaction in mink (Neovison vison) selected on ad libitum and restricted feeding V.H. Nielsen, S.H. Møller, B.K. Hansen, P. Berg Mink were selected for high November weight (AL line) and low feed conversion ratio (FC line) on ad libitum feeding and for high November weight on restricted feeding (RF line). After three generations of selection, the average estimated breeding value for November weight was 533, 326, and 150 g in males and 168, 82, and 85 g in females in the AL, RF, and FC lines. The breeding value for feed conversion ratio was 1.39, 0.84 and 0.68 kg feed kg 1 gain in males and 0.39, 0.31 and 0.23 kg feed kg 1 gain in females in the selection lines. In generation 4, the AL, RF and FC lines were tested on both ad libitum and restricted feeding. The estimated breeding value for November weight in males in the AL line (533 g) was significantly greater than that in the RF line (384 g) on ad libitum feeding. The corresponding values on restricted feeding were 297 and 326 g, respectively, which were not significantly different. This indicates genotype environment interaction. In the AL line, selection improved feed conversion ratio by increased appetite. In the RF line, it was improved by increased feed utilization. Environmental sensitivity in males, estimated from breeding values for November weight was 236 g in the AL line and 58 g in the RF line suggesting that the RF line was more robust to changes in feeding conditions. A smaller litter size in the AL line (4.1) than in the RF line (5.6) indicates that selection for large weight affects reproduction. Can J Anim Sci, 2011: 91(2), 231-237 On the origin of a domesticated species: Identifying the parent population of Russian silver foxes (Vulpes vulpes) M.J. Statham, L.N. Trut, B.N. Sacks, A.V. Kharlamova, I.N. Oskina, R.G. Gulevich, J.L. Johnson, S.V. Temnykh, G.M. Acland, A.V. Kukekova The foxes at Novosibirsk, Russia, are the only population of domesticated foxes in the world. These domesticated foxes originated from farm-bred silver foxes (Vulpes vulpes), whose genetic source is unknown. In this study we examined the origin of the domesticated strain of foxes and two other farmbred fox populations (aggressive and unselected) maintained in Novosibirsk. To identify the phylogenetic origin of these populations we sequenced two regions of mtdna, cytochrome b and D-loop, from 24 Novosibirsk foxes (8 foxes

20 Scientifur, Vol. 35, No. 2, 2011 from each population) and compared them with corresponding sequences of native red foxes from Europe, Asia, Alaska and Western Canada, Eastern Canada, and the Western Mountains of the USA. We identified seven cytochrome b - D-loop haplotypes in Novosibirsk populations, four of which were previously observed in Eastern North America. The three remaining haplotypes differed by one or two base change from the most common haplotype in Eastern Canada. Φ(ST) analysis showed significant differentiation between Novosibirsk populations and red fox populations from all geographic regions except Eastern Canada. No haplotypes of Eurasian origin were identified in the Novosibirsk populations. These results are consistent with historical records indicating that the original breeding stock of farm-bred foxes originated from Prince Edward Island, Canada. Mitochondrial DNA data together with historical records indicate two stages in the selection of domesticated foxes: the first includes captive breeding for ~50 years with unconscious selection for behaviour; the second corresponds to over 50 further years of intensive selection for tame behaviour. Biol J Linn Soc Lond, 2011: 103(1), 168-175 Stress and stereotypic behaviour in mink (Mustela vison): A focus on adrenocortical activity J. Malmkvist, L.L. Jeppesen, R. Palme We examined whether female mink with low (LS) and high (HS) occurrence of stereotypic behaviour differ in their adrenocortical activity in baseline conditions or in response to immobilisation (Experiment 1), handling, adrenocorticotropic hormone (ACTH) challenge (Experiment 2) and excretion of circulating cortisol (Experiment 3). Faeces are the predominating excretory route of cortisol (83%), with peak concentrations after 4.2 h (urine: 3.4 h). Faecal cortisol metabolites (FCMs) reflected changes in relation to handling/acth challenge. In Experiment 1 (n = 162), HS mink had approximately 54% higher baseline level of FCM than LS mink (P < 0.001), with markedly elevated FCM on the days after an immobilisation stressor. In Experiment 2 (n = 48), LS and HS mink did not differ in adrenocortical activity after an ACTH challenge. However, HS mink reacted more in response to handling, evident in the FCM level 4-20 h after the handling (P = 0.001). In Experiment 3 (n = 16), the excretion of infused (3)H-cortisol did not differ between LS and HS mink. Stereotypic behaviour is concurrent with higher baseline concentrations of FCM, which cannot be explained by a greater adrenocortical reactivity or a different excretion of the circulating cortisol. Instead, we conclude that mink with a high level of stereotypic behaviour have a greater perception of stress, or increased sensitivity to stressors at the pituitary level. Stress, 2011: Mar 27. [Epub ahead of print] Pregnancy Detection in Putatively Unmated Mink (Mustela vison) by Serum Progesteron Level L. Felska-Blaszczyk, B. Lasota, M. Sulik, A. Maslowska, M. Dziadosz, B. Blaszczyk, P. Blaszczyk The aim of this study was to determine whether blood plasma progesterone is a reliable indicator of pregnancy in mink at an early stage of gestation. We also attempted to establish the threshold value of progesterone as a pregnancy indicator. The analysis was carried out at a production farm on 42 standard female mink aged 1 year, which were grouped both according to the observed success of mating ("mated" and "unmated") and the level of blood serum progesterone measured afterwards ("pregnant" and "nonpregnant"). It was next verified whether a particular female had been assigned to the proper group in the first place. An analysis of accuracy of mating success assessment within the group of unmated females revealed that more than one-third of decisions were wrong, since some females that had been considered unmated ultimately whelped. This suggests that mating supervision by farm workers lacks reliability. A progesterone test for verification of such management decisions should limit the risk of error. We suggest that progesterone tests could be carried out using the threshold values 1.9 ng/ml and 20 ng/ml in blood sampled on 25 March and 8 April, respectively, although some level of uncertainty should be taken into account. J Reprod Dev, 2011: Mar 8. [Epub ahead of print]

Abstracts. 21 Effect of mutations affecting coat color on the blood lymphocyte structure in the American mink (Mustela vison Schreber, 1777) L.B. Uzenbaeva, O.V. Trapezov, A.G. Kizhina, V.A. Iliukha, L.I. Trapezova, N.N. Tiutiunnik American minks with different genotypes containing the Aleutian coat color allele in the homozygous state, including the single recessive Aleutian (a/a); double recessive sapphire (a/a p/p) and lavender (m/m a/a); triple recessive violet (m/m a/a p/p); and dominant-recessive cross sapphire (S/+ a/a p/p), sapphire leopard (S(K)/+ a/a p/p), and shadow sapphire (S(H)/+ a/a p/p) minks, as well as American minks without the Aleutian allele, including the standard (+/+); single recessive silverblue (p/p) and hedlund-white (h/h); double recessive pearl (k/k p/p), Finnish topaz (t(s)/t(s) b/b); incompletely dominant royal silver (S(R)/+), standard leopard (S(K)/+), and black crystal (C(R)/+); and dominant-recessive snowy topaz (C(R)/+ t(s)/t(s) b/b) and Kujtezhy-spotted (S(K)/+ b/b) minks have been studied. Homozygosity for the a allele has been found to disturb the subcellular structure of leukocyte, namely the formation of abnormally large granules. Genetika, 2011: 47(1), 87-94 Differentiation of canine distemper virus isolates in fur animals from various vaccine strains by reverse transcription-polymerase chain reactionrestriction fragment length polymorphism according to phylogenetic relations in china F. Wang, X. Yan, X. Chai, H. Zhang, J. Zhao, Y. Wen, W. Wu In order to effectively identify the vaccine and field strains of Canine distemper virus (CDV), a new differential diagnostic test has been developed based on reverse transcription-polymerase chain reaction (RT-PCR) and restriction fragment length polymorphism (RFLP). We selected an 829 bp fragment of the nucleoprotein (N) gene of CDV. By RFLP analysis using BamHI, field isolates were distinguishable from the vaccine strains. Two fragments were obtained from the vaccine strains by RT-PCR-RFLP analysis while three were observed in the field strains. An 829 nucleotide region of the CDV N gene was analyzed in 19 CDV field strains isolated from minks, raccoon dogs and foxes in China between 2005 and 2007. The results suggest this method is precise, accurate and efficient. It was also determined that three different genotypes exist in CDV field strains in fur animal herds of the north of China, most of which belong to Asian type. Mutated field strains, JSY06-R1, JSY06-R2 and JDH07-F1 also exist in Northern China, but are most closely related to the standard virulent strain A75/17, designated in Arctic and America-2 genetype in the present study, respectively. Virol J, 2011: 8, 85 Histopathologic and immunohistochemical lesions in liver of mink infected with Aleutian disease virus A. Valdovska, M. Pilmane Parvovirus of Aleutian disease causes mainly damage to kidneys, but immune complexes deposition and damage may occur also in other organs. In mink farms of Latvia the liver dystrophy or hepatic lipidosis of mink is widely distributed. The goal of this study was to examine probability of liver damage and regeneration of mink infected with Aleutian disease virus. Liver injury was assessed histologically. The mink liver demonstrated inflammation of liver parenchyma and foci of fatty liver. In immunohistochemistry, during liver regeneration the matrix metalloproteinases MMP-9, vascular endothelial growth factor and beta-defensin 2 expressions were lower, but MMP-2 and nerve growth factor receptor p75 expression was increased. Pol J Vet Sci, 2011:14(1), 69-76 Molecular characterization of a new species in the genus Alphacoronavirus associated with mink epizootic catarrhal gastroenteritis A.N. Vlasova, R. Halpin, S. Wang, E. Ghedin, D.J. Spiro, L.J. Saif A coronavirus (CoV) previously shown to be associated with catarrhal gastroenteritis in mink (Mustela vison) was identified by electron microscopy in mink faeces from two fur farms in

22 Scientifur, Vol. 35, No. 2, 2011 Wisconsin and Minnesota in 1998. A pancoronavirus and a genus-specific RT-PCR assay were used initially to demonstrate that the newly discovered mink CoVs (MCoVs) were members of the genus Alphacoronavirus. Subsequently, using a random RT-PCR approach, full-genomic sequences were generated that further confirmed that, phylogenetically, the MCoVs belonged to the genus Alphacoronavirus, with closest relatedness to the recently identified but only partially sequenced (fragments of the polymerase, and full-length spike, 3c, envelope, nucleoprotein, membrane, 3x and 7b genes) ferret enteric coronavirus (FRECV) and ferret systemic coronavirus (FRSCV). The molecular data presented in this study provide the first genetic evidence for a new coronavirus associated with epizootic catarrhal gastroenteritis outbreaks in mink and demonstrate that MCoVs possess high genomic variability and relatively low overall nucleotide sequence identities (91.7 %) between contemporary strains. Additionally, the new MCoVs appeared to be phylogenetically distant from human (229E and NL63) and other alphacoronaviruses and did not belong to the species Alphacoronavirus 1. It is proposed that, together with the partially sequenced FRECV and FRSCV, they comprise a new species within the genus Alphacoronavirus. J Gen Virol, 2011: 92, 1369-79

INSTRUCTIONS FOR AUTHORS SCIENTIFUR is published as four issues per year in the following way: Three issues containing short communications (max. 4 pages), abstracts, letters, book reviews etc. One issue entitled Fur Animal Science containing only reviewed articles SCIENTIFIC REVIEWED ARTICLES should not exceed 6 printed pages (=12 typewritten A4 pages with double spacing including figures and tables). Additional pages will be charged to the author(s) at Euro 100 per printed page. Scientific reviewed articles will be sent to two referees for scientific approval. Papers submitted for publication as scientific reviewed articles are received with the understanding that the work has not been published before, and is not considered for publication elsewhere and has been read and approved by all authors. Animal experimental methods reported in SCIENTIFUR should meet ethical standards of animal treatment. SHORT COMMUNICATIONS. Other original papers can be published in SCIENTIFUR as short communications. In regard to such articles the author(s) alone is (are) responsible for the scientific validity of the article. Such papers must not exceed 4 printed pages. Please indicate if an original article should be published as a Scientific Reviewed Article or as a Short Communication. MANUSCRIPTS All manuscripts must be sent in three copies and preferably accompanied by an electronic copy on a diskette or by E-mail. The electronic files should preferably be in Microsoft Word. The material should be sent to: SCIENTIFUR/Faculty of Agricultural Sciences, Aarhus University, P.O. Box 14, DK-8830 Tjele, Denmark or E-mail: Scientifur@agrsci.dk Manuscripts must be in English, typed double spaced with page and line numbering and consisting of: Title, which should be concise and informative, but as short as possible, and contain the main key words. Authors name(s) as well as name(s) and address(es) of the institutions to which the work is attributed. E-mail address of the corresponding author should preferably be included. Summary/Abstract, which should not exceed 150 words. Keywords in alphabetic order if not included in the title. Text. The text should normally be divided into: Introduction, Material and Methods, Results, Discussion, Acknowledgements and References and follow the internationally accepted rules. Double documentation in both figures and tables will not be accepted. Illustrations. All graphs, photos and pictures are considered as figures and have to be labelled on the reversed side of the sheet with number, authors name and indication of orientation. All drawings have to be professionally drafted (photocopies are not an acceptable standard). The illustrations included in the electronic version should be as JPG-, GIF- or TIF-files. Any halftones must exhibit high contrast and text and other details must be large enough to retain the readability after reduction of figure size to single column (width 80 mm); the width of 170 mm can be accepted in special cases. Colour illustrations can be included in the electronic version of SCIENTIFUR. Any colour illustrations in the printed copies must be paid by the author. Tables. Each table should be typed on a separate page. Tables must be numbered consecutively with Arabic numerals, and have a self-explanatory title. Tables should be planned to fit a final width of 80 or 170 mm. References should be kept to a pertinent minimum. References in the text should be made according to the following examples: Nielsen, 1992; Hansen & Berg, 1993; Bakken et al., 1999. The list of references should be arranged in alphabetic order according to the name of the first author and the year of publication within the names. The year of publication should be written between the name(s) and the title. Reprints. After publication of a reviewed article the authors receive 25 reprints without charges. Additional reprints can be ordered from the editor after individual agreement.