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Does Small Ruminant Lentivirus Infection in Goats Predispose to Bacterial Infection of the Mammary Gland? A Preliminary Study

dc.contributor.authorJarczak, Justyna
dc.contributor.authorUrbańska, Daria
dc.contributor.authorPuchała, Ryszard
dc.contributor.authorCzopowicz, Michał
dc.contributor.authorKaba, Jarosław
dc.contributor.authorHorbańczuk, Karina
dc.contributor.authorBagnicka, Emilia
dc.date.accessioned2021-10-13T05:13:45Z
dc.date.available2021-10-13T05:13:45Z
dc.date.issued2021
dc.identifier.citationUrbańska, D.; Puchała, R.; Jarczak, J.; Czopowicz, M.; Kaba, J.; Horbańczuk, K.; Bagnicka, E. Does Small Ruminant Lentivirus Infection in Goats Predispose to Bacterial Infection of the Mammary Gland? A Preliminary Study. Animals 2021, 11, 1851.pl_PL
dc.identifier.issn2076-2615
dc.identifier.urihttp://hdl.handle.net/11089/39369
dc.description.abstractThe aim of this study was to determine whether asymptomatic small ruminant lentivirus seropositive (SRLV-SP) goats were more susceptible to bacterial infection of the udder when lactating by comparing the presence and species of pathogenic bacteria in their milk with the values for seronegative goats (SRLV-SN). Milk samples were collected during morning milking on days 20, 40, 60, 150, and 210 of lactation for three consecutive years and subjected to bacteriological examination. Staphylococcus caprae and S. xylosus were the most frequent strains identified in both SRLV-SP and SRLV-SN goats. The prevalence of pathogenic bacteria was the highest in the 1st lactation, regardless of SRLV status. Moreover, the prevalence of pathogenic bacteria was significantly higher in SRLV-SP goats, but only those in the 5th or further lactation (p = 0.010). This suggests a relationship between long-lasting SRLV infection and susceptibility to bacterial infections of the udder.pl_PL
dc.language.isoenpl_PL
dc.publisherMDPIpl_PL
dc.relation.ispartofseriesAnimals;11, 1851
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectcaprine arthritis-encephalitispl_PL
dc.subjectmastitispl_PL
dc.subjectparitypl_PL
dc.subjectpathogenic bacteriapl_PL
dc.subjectpolish white improvedpl_PL
dc.subjectpolish fawn improvedpl_PL
dc.subjectsmall ruminantspl_PL
dc.subjectudderpl_PL
dc.titleDoes Small Ruminant Lentivirus Infection in Goats Predispose to Bacterial Infection of the Mammary Gland? A Preliminary Studypl_PL
dc.typeArticlepl_PL
dc.page.number11pl_PL
dc.contributor.authorAffiliationBiobank Lab, Department of Molecular Biophysics, University of Łódź, Pomorska 139, 90-235 Łódź, Polandpl_PL
dc.contributor.authorAffiliationInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Postepu 36A, 05-552 Jastrzębiec, Polandpl_PL
dc.contributor.authorAffiliationApplied Physiology Unit, Military Institute of Hygiene and Epidemiology, Kozielska 4, 01-001 Warsaw, Polandpl_PL
dc.contributor.authorAffiliationDivision of Veterinary Epidemiology and Economics, Institute of Veterinary Medicine, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159c, 02-776 Warsaw, Polandpl_PL
dc.contributor.authorAffiliationDivision of Veterinary Epidemiology and Economics, Institute of Veterinary Medicine, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159c, 02-776 Warsaw, Polandpl_PL
dc.contributor.authorAffiliationInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Postepu 36A, 05-552 Jastrzębiec, Polandpl_PL
dc.contributor.authorAffiliationInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Postepu 36A, 05-552 Jastrzębiec, Polandpl_PL
dc.referencesSpuria, L.; Biasibetti, E.; Bisanzio, N.; Biasato, I.; De Meneghi, D.; Nebbia, P.; Robino, P.; Bianco, P.; Lamberti, M.; Caruso, C.; et al. Microbial agents in macroscopically healthy mammary gland tissues of small ruminants. PeerJ 2017, 5, e3994.pl_PL
dc.referencesBagnicka, E.; Winnicka, A.; Jóźwik, A.; Rzewuska, M.; Strzałkowska, N.; Kościuczuk, E.; Prusak, B.; Kaba, J.; Horbańczuk, J.; Krzyżewski, J. Relationship between somatic cell count and bacterial pathogens in goat milk. ˙ Small Rumin. Res. 2011, 100, 72–77.pl_PL
dc.referencesVanselow, J.; Yang, W.; Herrmann, J.; Zerbe, H.; Schuberth, H.-J.; Petzl, W.; Tomek, W.; Seyfert, H.-M. DNA-remethylation around a STAT5-binding enhancer in the αS1-casein promoter is associated with abrupt shutdown of αS1-casein synthesis during acute mastitis. J. Mol. Endocrinol. 2006, 37, 463–477.pl_PL
dc.referencesContreras, A.; Luengo, C.; Sánchez, A.; Corrales, J. The role of intramammary pathogens in dairy goats. Livest. Prod. Sci. 2003, 79, 273–283.pl_PL
dc.referencesStuhr, T.A.K. Intramammary infections in dairy goats: Recent knowledge and indicators for detection of subclinical mastitis. Landbauforsch. vTI Agric. For. Res. 2010, 4, 267–280.pl_PL
dc.referencesBergonier, D.; Rupp, R.; Lagriffoul, G.; Berthelot, X. Mastitis of dairy small ruminants. Veter. Res. 2003, 34, 689–716.pl_PL
dc.referencesRainard, P.; Gitton, C.; Chaumeil, T.; Fassier, T.; Huau, C.; Riou, M.; Tosser-Klopp, G.; Krupova, Z.; Chaize, A.; Gilbert, F.B.; et al. Host factors determine the evolution of infection with Staphylococcus aureus to gangrenous mastitis in goats. Veter. Res. 2018, 49, 1–17.pl_PL
dc.referencesJohler, S.; Giannini, P.; Jermini, M.; Hummerjohann, J.; Baumgartner, A.; Stephan, R. Further evidence for staphylococcal food poisoning outbreaks caused by egc-encoded enterotoxins. Toxins 2015, 7, 997–1004.pl_PL
dc.referencesDeinhofer, M.; Pernthaner, A. Differenzierung von Staphylokokken aus Schaf-und Ziegenmilchproben [Differentiation of staphylococci from sheep and goat milk samples]. Deutsche Tierärztliche Wochenschr. 1993, 100, 234–236.pl_PL
dc.referencesDeinhofer, M. Staphylococcus spp. as mastitis-related pathogens in goat milk. Veter. Microbiol. 1995, 43, 161–166.pl_PL
dc.referencesJiménez, G.E.A.; Pérez, J.L.T.; Murillo, C.R.; Reynoso, B.A.; Álvarez, H.R. Serotyping versus genotyping in infected sheep and goats with small ruminant lentiviruses. Veter. Microbiol. 2021, 252, 108931.pl_PL
dc.referencesOlech, M.; Kuźmak, J. Molecular Characterization of Small Ruminant Lentiviruses of Subtype A5 Detected in Naturally Infected but Clinically Healthy Goats of Carpathian Breed. Pathogens 2020, 9, 992.pl_PL
dc.referencesOlech, M.; Rachid, A.; Croisé, B.; Kuźmak, J.; Valas, S. Genetic and antigenic characterization of small ruminant lentiviruses circulating in Poland. Virus Res. 2012, 163, 528–536.pl_PL
dc.referencesOlech, M.; Valas, S.; Kuźmak, J. Epidemiological survey in single-species flocks from Poland reveals expanded genetic and antigenic diversity of small ruminant lentiviruses. PLoS ONE 2018, 13, e0193892.pl_PL
dc.referencesBlacklaws, B.A. Small ruminant lentiviruses: Immunopathogenesis of visna-maedi and caprine arthritis and encephalitis virus. Comp. Immunol. Microbiol. Infect. Dis. 2012, 35, 259–269.pl_PL
dc.referencesNowicka, D.; Czopowicz, M.; Szaluś-Jordanow, O.; Witkowski, L.; Bagnicka, E.; Kaba, J. Seropositive bucks and within-herd prevalence of small ruminant lentivirus infection. Central Eur. J. Immunol. 2015, 3, 283–286.pl_PL
dc.referencesLarruskain, A.; Jugo, B.M. Retroviral infections in sheep and goats: Small ruminant lentiviruses and host interaction. Viruses 2013, 5, 2043–2061.pl_PL
dc.referencesShah, C.; Huder, J.B.; Böni, J.; Schönmann, M.; Mühlherr, J.; Lutz, H.; Schupbach, J. Direct evidence for natural transmission of small-ruminant lentiviruses of subtype A4 from goats to sheep and vice versa. J. Virol. 2004, 78, 7518–7522.pl_PL
dc.referencesStonos, N.; Wootton, S.K.; Karrow, N. Immunogenetics of small ruminant lentiviral infections. Viruses 2014, 6, 3311–3333.pl_PL
dc.referencesJarczak, J.; Kościuczuk, E.; Ostrowska, M.; Lisowski, P.; Strzałkowska, N.; Jóźwik, A.; Krzyżewski, J.; Zwierzchowski, L.; ˙ Słoniewska, D.; Bagnicka, E. The effects of diet supplementation with yeast on the expression of selected immune system genes in the milk somatic cells of dairy goats. Anim. Sci. Pap. Rep. 2014, 32, 41–53.pl_PL
dc.referencesJarczak, J.; Słoniewska, D.; Kaba, J.; Bagnicka, E. The expression of cytokines in the milk somatic cells, blood leukocytes and serum of goats infected with small ruminant lentivirus. BMC Veter. Res. 2019, 15, 1–11.pl_PL
dc.referencesReczyńska, D.; Zalewska, M.; Czopowicz, M.; Kaba, J.; Zwierzchowski, L.; Bagnicka, E. Small ruminant lentivirus infection influences expression of acute phase proteins and cathelicidin genes in milk somatic cells and peripheral blood leukocytes of dairy goats. Veter. Res. 2018, 49, 1–13.pl_PL
dc.referencesPaiva, C.N.; Bozza, M.T. Are Reactive Oxygen Species Always Detrimental to Pathogens? Antioxid. Redox Signal. 2014, 20, 1000–1037.pl_PL
dc.referencesAsadpour, R.; Paktinat, S.; Ghassemi, F.; Jafari, R. Study on Correlation of Maedi-Visna Virus (MVV) with Ovine Subclinical Mastitis in Iran. Indian J. Microbiol. 2013, 54, 218–222.pl_PL
dc.referencesHouwers, D.J.; Pekelder, J.J.; Akkermans, J.W.; Van Der Molen, E.J.; Schreuder, B. Incidence of indurative lymphocytic mastitis in a flock of sheep infected with maedi-visna virus. Veter. Rec. 1988, 122, 435–437.pl_PL
dc.referencesRyan, D.P.; Greenwood, P.L.; Nicholls, P.J. Effect of caprine arthritis-encephalitis virus infection on milk cell count and N-acetyl-β– glucosaminidase activity in dairy goats. J. Dairy Res. 1993, 60, 299–306.pl_PL
dc.referencesSmith, M.C.; Cutlip, R. Effects of infection with caprine arthritis-encephalitis virus on milk production in goats. J. Am. Veter. Med Assoc. 1988, 193, 63–67.pl_PL
dc.referencesTariba, B.; Kosteli´c, A.; Šalamon, D.; Roi´c, B.; Beni´c, M.; Prvanovi´c Babi´c, N.; Salajpal, K. Subclinical mastitis and clinical arthritis in French Alpine goats serologically positive for caprine artritis-encephalitis virus. Vet. Arh. 2017, 87, 121–128.pl_PL
dc.referencesNord, K. CAEV Infection does not Affect Prevalence of Bacterial Mastitis in Goats. Acta Veter. Scand. 1997, 38, 197–199.pl_PL
dc.referencesNowicka, D.; Czopowicz, M.; Mickiewicz, M.; Szaluś-Jordanow, O.; Witkowski, L.; Bagnicka, E.; Kaba, J. Diagnostic performance of ID Screen® MVV-CAEV Indirect Screening ELISA in identifying small ruminant lentiviruses-infected goats. Pol. J. Veter. Sci. 2014, 17, 501–506.pl_PL
dc.referencesBrinkhof, J.; Van Maanen, C.; Wigger, R.; Peterson, K.; Houwers, D. Specific detection of small ruminant lentiviral nucleic acid sequences located in the proviral long terminal repeat and leader-gag regions using real-time polymerase chain reaction. J. Virol. Methods 2008, 147, 338–344.pl_PL
dc.referencesBagnicka, E.; Distl, O.; Hamann, H.; Łukaszewicz, M. Heritabilities and genetic correlations between the dairy traits in goats estimated in first vs later lactations. Anim. Sci. Pap. Rep. 2004, 2, 205–213.pl_PL
dc.referencesBagnicka, E.; Łukaszewicz, M.; Ådnøy, T. Genetic parameters of somatic cell score and lactose content in goat’s milk. J. Anim. Feed. Sci. 2016, 25, 210–215.pl_PL
dc.referencesNowicka, D.; Czopowicz, M.; Bagnicka, E.; Rzewuska, M.; Strzałkowska, N.; Kaba, J. Influence of small ruminant lentivirus infection on cheese yield in goats. J. Dairy Res. 2015, 82, 102–106.pl_PL
dc.referencesContreras, A.; Paape, M.; Miller, R.; Contreras, A.; Paape, M.; Miller, R. Prevalence of subclinical intramammary infection caused by Staphylococcus epidermidis in a commercial dairy goat herd. Small Rumin. Res. 1999, 31, 203–208.pl_PL
dc.referencesBoscos, C.; Stefanakis, A.; Alexopoulos, C.; Samartzi, F. Prevalence of subclinical mastitis and influence of breed, parity, stage of lactation and mammary bacteriological status on Coulter Counter Counts and California Mastitis Test in the milk of Saanen and autochthonous Greek goats. Small Rumin. Res. 1996, 21, 139–147.pl_PL
dc.referencesPeterson, R.; Hariharan, H.; Matthew, V.; Stratton, G.; Hegamin-Younger, C.; Sharma, R. Comparison of Culture of Goat Milk with Indirect Measurement of Somatic Cell Count Using a Commercial Kit, and Antimicrobial Susceptibility of Bacterial Isolates. Int. J. Veter. Med. Res. Rep. 2014, 1–6.pl_PL
dc.referencesVirdis, S.; Scarano, C.; Cossu, F.; Spanu, V.; Spanu, C.; De Santis, E.P.L. Antibiotic Resistance inStaphylococcus aureusand Coagulase Negative Staphylococci Isolated from Goats with Subclinical Mastitis. Veter. Med. Int. 2010, 2010, 1–6.pl_PL
dc.referencesEl-Jakee, J.K.; Aref, N.E.; Gomaa, A.; ElHariri, M.; Galal, H.M.; Omar, S.A.; Samir, A. Emerging of coagulase negative staphylococci as a cause of mastitis in dairy animals: An environmental hazard. Int. J. Veter. Sci. Med. 2013, 1, 74–78.pl_PL
dc.referencesGuimarães, F.; Nóbrega, D.; Pereira, V.; Marson, P.M.; Pantoja, J.C.D.F.; Langoni, H. Enterotoxin genes in coagulase-negative and coagulase-positive staphylococci isolated from bovine milk. J. Dairy Sci. 2013, 96, 2866–2872.pl_PL
dc.referencesZalewska, M.; Kawecka-Grochocka, E.; Słoniewska, D.; Ko´sciuczuk, E.; Marczak, S.; Jarmuz, W.; Zwierzchowski, L.; Bagnicka, E. ˙ Acute phase protein expressions in secretory and cistern lining epithelium tissues of the dairy cattle mammary gland during chronic mastitis caused by staphylococci. BMC Veter. Res. 2020, 16, 1–9.pl_PL
dc.referencesDeubelbeiss, M.; Blatti-Cardinaux, L.; Zahno, M.-L.; Zanoni, R.; Vogt, H.-R.; Posthaus, H.; Bertoni, G. Characterization of small ruminant lentivirus A4 subtype isolates and assessment of their pathogenic potential in naturally infected goats. Virol. J. 2014, 11, 65.pl_PL
dc.referencesGosselin, V.B.; Dufour, S.; Calcutt, M.J.; Adkins, P.R.; Middleton, J.R. Staphylococcal intramammary infection dynamics and the relationship with milk quality parameters in dairy goats over the dry period. J. Dairy Sci. 2019, 102, 4332–4340pl_PL
dc.referencesGelasakis, A.; Angelidis, A.; Giannakou, R.; Arsenos, G. Bacterial subclinical mastitis and its effect on milk quality traits in low-input dairy goat herds. Veter. Rec. 2018, 183, 449.pl_PL
dc.referencesMahlangu, P.; Maina, N.; Kagira, J. Prevalence, Risk Factors, and Antibiogram of Bacteria Isolated from Milk of Goats with Subclinical Mastitis in Thika East Subcounty, Kenya. J. Veter. Med. 2018, 2018, 1–8.pl_PL
dc.referencesSánchez, A.; Contreras, A.; Corrales, J. Parity as a risk factor for caprine subclinical intramammary infection. Small Rumin. Res. 1999, 31, 197–201.pl_PL
dc.referencesMilczarek, M.; Czopowicz, M.; Witkowski, L.; Bereznowski, A.; Bagnicka, E.; Kosieradzka, I.; Kaba, J. Metabolomic profile of adult Saanen goats infected with small ruminant lentivirus. Small Rumin. Res. 2019, 170, 12–18.pl_PL
dc.identifier.doi10.3390/ani11071851
dc.disciplinenauki biologicznepl_PL


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