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Journal articles on the topic 'Cattle shipping disease'
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1
Dabo, S. M., J. D. Taylor, and A. W. Confer. "Pasteurella multocidaand bovine respiratory disease." Animal Health Research Reviews 8, no. 2 (December 2007): 129–50. http://dx.doi.org/10.1017/s1466252307001399.
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AbstractPasteurella multocidais a pathogenic Gram-negative bacterium that has been classified into three subspecies, five capsular serogroups and 16 serotypes.P. multocidaserogroup A isolates are bovine nasopharyngeal commensals, bovine pathogens and common isolates from bovine respiratory disease (BRD), both enzootic calf pneumonia of young dairy calves and shipping fever of weaned, stressed beef cattle.P. multocidaA:3 is the most common serotype isolated from BRD, and these isolates have limited heterogeneity based on outer membrane protein (OMP) profiles and ribotyping. Development ofP. multocida-induced pneumonia is associated with environmental and stress factors such as shipping, co-mingling, and overcrowding as well as concurrent or predisposing viral or bacterial infections. Lung lesions consist of an acute to subacute bronchopneumonia that may or may not have an associated pleuritis. Numerous virulence or potential virulence factors have been described for bovine respiratory isolates including adherence and colonization factors, iron-regulated and acquisition proteins, extracellular enzymes such as neuraminidase, lipopolysaccharide, polysaccharide capsule and a variety of OMPs. Immunity of cattle against respiratory pasteurellosis is poorly understood; however, high serum antibodies to OMPs appear to be important for enhancing resistance to the bacterium. Currently availableP. multocidavaccines for use in cattle are predominately traditional bacterins and a live streptomycin-dependent mutant. The field efficacy of these vaccines is not well documented in the literature.
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Storz, Johannes, Xiaoqing Lin, Charles W. Purdy, Vladimir N. Chouljenko, Konstantin G. Kousoulas, Frederick M. Enright, William C. Gilmore, Robert E. Briggs, and Raymond W. Loan. "Coronavirus and Pasteurella Infections in Bovine Shipping Fever Pneumonia and Evans' Criteria for Causation." Journal of Clinical Microbiology 38, no. 9 (2000): 3291–98. http://dx.doi.org/10.1128/jcm.38.9.3291-3298.2000.
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Respiratory tract infections with viruses andPasteurella spp. were determined sequentially among 26 cattle that died during two severe epizootics of shipping fever pneumonia. Nasal swab and serum samples were collected prior to onset of the epizootics, during disease progression, and after death, when necropsies were performed and lung samples were collected. Eighteen normal control cattle also were sampled at the beginning of the epizootics as well as at weekly intervals for 4 weeks. Respiratory bovine coronaviruses (RBCV) were isolated from nasal secretions of 21 and 25 cattle before and after transport. Two and 17 cattle nasally shed Pasteurella spp. before and after transport, respectively. RBCV were isolated at titers of 1 × 103to 1.2 × 107 PFU per g of lung tissue from 18 cattle that died within 7 days of the epizootics, but not from the lungs of the remaining cattle that died on days 9 to 36. Twenty-five of the 26 lung samples were positive for Pasteurella spp., and their CFU ranged between 4.0 × 105 and 2.3 × 109 per g. Acute and subacute exudative, necrotizing lobar pneumonia characterized the lung lesions of these cattle with a majority of pneumonic lung lobes exhibiting fibronecrotic and exudative changes typical of pneumonic pasteurellosis, but other lung lobules had histological changes consisting of bronchiolitis and alveolitis typical of virus-induced changes. These cattle were immunologically naive to both infectious agents at the onset of the epizootics, but those that died after day 7 had rising antibody titers against RBCV andPasteurella haemolytica. In contrast, the 18 clinically normal and RBCV isolation-negative cattle had high hemagglutinin inhibition antibody titers to RBCV from the beginning, while their antibody responses to P. haemolytica antigens were delayed. Evans' criteria for causation were applied to our findings because of the multifactorial nature of shipping fever pneumonia. This analysis identified RBCV as the primary inciting cause in these two epizootics. These viruses were previously not recognized as a causative agent in this complex respiratory tract disease of cattle.
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Lin, Xiaoqing, Kathy L. O'Reilly, Mamie L. Burrell, and Johannes Storz. "Infectivity-Neutralizing and Hemagglutinin-Inhibiting Antibody Responses to Respiratory Coronavirus Infections of Cattle in Pathogenesis of Shipping Fever Pneumonia." Clinical Diagnostic Laboratory Immunology 8, no. 2 (March 1, 2001): 357–62. http://dx.doi.org/10.1128/cdli.8.2.357-362.2001.
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ABSTRACT Respiratory bovine coronaviruses (RBCV) emerged as an infectious agent most frequently isolated from respiratory tract samples of cattle with acute respiratory tract diseases. Infectivity-neutralizing (IN) and hemagglutinin-inhibiting (HAI) antibodies induced by RBCV infections were monitored in sequential serum samples collected from cattle during a naturally evolving and experimentally monitored epizootic of shipping fever pneumonia (SFP). Cattle nasally shedding RBCV at the beginning of the epizootic started with low levels of serum IN and HAI antibodies. An increase in serum IN antibody after day 7 led to reduction of virus shedding in nasal secretions by the majority of the cattle between days 7 and 14. A substantial rise in the serum HAI antibody was observed during the initial phase among the sick but not the clinically normal cattle which were infected with RBCV. The RBCV isolation-positive cattle that developed fatal SFP had minimal serum IN and HAI antibodies during the course of disease development. Cattle that remained negative in RBCV isolation tests entered this epizootic with high levels of serum IN and HAI antibodies, which dramatically increased during the next two weeks. Protection against SFP was apparently associated with significantly higher levels of serum IN antibodies at the beginning of the epizootic. The RBCV-neutralizing activity is associated with serum immunoglobulin G (IgG), particularly the IgG2 subclass, while RBCV-specific HAI antibody is related to both serum IgG and IgM fractions.
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Tsao, Kimberly, Stefan Sellman, Lindsay M. Beck-Johnson, Deedra J. Murrieta, Clayton Hallman, Tom Lindström, Ryan S. Miller, Katie Portacci, Michael J. Tildesley, and Colleen T. Webb. "Effects of regional differences and demography in modelling foot-and-mouth disease in cattle at the national scale." Interface Focus 10, no. 1 (December 13, 2019): 20190054. http://dx.doi.org/10.1098/rsfs.2019.0054.
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Foot-and-mouth disease (FMD) is a fast-spreading viral infection that can produce large and costly outbreaks in livestock populations. Transmission occurs at multiple spatial scales, as can the actions used to control outbreaks. The US cattle industry is spatially expansive, with heterogeneous distributions of animals and infrastructure. We have developed a model that incorporates the effects of scale for both disease transmission and control actions, applied here in simulating FMD outbreaks in US cattle. We simulated infection initiating in each of the 3049 counties in the contiguous US, 100 times per county. When initial infection was located in specific regions, large outbreaks were more likely to occur, driven by infrastructure and other demographic attributes such as premises clustering and number of cattle on premises. Sensitivity analyses suggest these attributes had more impact on outbreak metrics than the ranges of estimated disease parameter values. Additionally, although shipping accounted for a small percentage of overall transmission, areas receiving the most animal shipments tended to have other attributes that increase the probability of large outbreaks. The importance of including spatial and demographic heterogeneity in modelling outbreak trajectories and control actions is illustrated by specific regions consistently producing larger outbreaks than others.
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Amer, Haitham Mohamed. "Bovine-like coronaviruses in domestic and wild ruminants." Animal Health Research Reviews 19, no. 2 (December 2018): 113–24. http://dx.doi.org/10.1017/s1466252318000117.
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AbstractCoronaviruses (CoVs) produce a wide spectrum of disease syndromes in different mammalian and avian host species. These viruses are well-recognized for their ability to change tissue tropism, to hurdle the interspecies barriers and to adapt ecological variations. It is predicted that the inherent genetic diversity of CoVs caused by accumulation of point mutations and high frequency of homologous recombination is the principal determinant of these competences. Several CoVs (e.g. Severe acute respiratory syndrome-CoV, Middle East respiratory syndrome-CoV) have been recorded to cross the interspecies barrier, inducing different disease conditions in variable animal hosts. Bovine CoV (BCoV) is a primary cause of gastroenteritis and respiratory disease in cattle calves, winter dysentery in lactating cows and shipping fever pneumonia in feedlot cattle. Although it has long been known as a restrictive cattle pathogen, CoVs that are closely related to BCoV have been recognized in dogs, humans and in other ruminant species. Biologic, antigenic and genetic analyses of the so-called ‘bovine-like CoVs’ proposed classification of these viruses as host-range variants rather than distinct virus species. In this review, the different bovine-like CoVs that have been identified in domesticated ruminants (water buffalo, sheep, goat, dromedary camel, llama and alpaca) and wild ruminants (deer, wild cattle, antelopes, giraffes and wild goats) are discussed in terms of epidemiology, transmission and virus characteristics. The presented data denote the importance of these viruses in the persistence of BCoV in nature, spread to new geographical zones, and continuous emergence of disease epidemics in cattle farms.
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Johnson, Bradley J., and Zachary K. Smith. "219 Managing Beef Cattle Growth Amidst a Global Pandemic: Lessons Learned from 2020 and Strategies for the Future." Journal of Animal Science 99, Supplement_1 (May 1, 2021): 38. http://dx.doi.org/10.1093/jas/skab054.066.
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Abstract The coronavirus disease-19 related events of 2020 had severe detrimental effects on meat animal production in the United State. Due to harvest facility slowdowns and shutdowns, many market animals, including beef cattle, were on feed greater than 60 d past their optimal endpoint. These dramatic changes caused many changes in feeding and growth technologies management. The two major growth enhancing compounds used in feedlot cattle production are steroidal implants (IMP) and β-adrenergic agonists (β-AA). Implementation of β-AA during the pandemic was extremely difficult due to the lack of knowledge on exact shipping dates. The β-AA are fed the last 28 to 42 d on feed. Ractopamine was approved for cattle with essential a 12-h withdrawal. Many questions arose about the maximum length of withdrawal on ractopamine before losing any of the added growth response in both the live animal and carcass. Many feedlot operators relied on IMP administration to achieve added growth response in cattle held for longer days on feed. With zero-day withdrawal on implants, it was a cost-effective means to hold cattle in an efficient manner. Many producers simply could not manage β-AA feeding during the pandemic period and used other management technologies to enhance growth and efficiency during the end of the feeding period.
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Mackenzie, A. M., M. Drennan, T. G. Rowan, S. D. Carter, J. B. Dixon, and J. Tebble. "Effect of Transportation and Husbandry on Humoral Immune Responses in Suckler Calves." Proceedings of the British Society of Animal Production (1972) 1993 (March 1993): 77. http://dx.doi.org/10.1017/s030822960002403x.
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The trade between European community (EC) countries involving the transportation of live calves has, with the advent of 1993, considerably increased. In the UK alone, thousands of calves are transported on lorries and ferries and exported to other EC countries each year. An increase in the incidence of ‘shipping fever’, the general classification in American feedlots for bacterial or viral respiratory infections in cattle, has been observed following transportation. Further observations have shown an increased disease susceptibility following transportation and research has suggested that this is due to immunosuppression. An experiment was designed to investigate the effects of transportation and other normal husbandry variables on their ability to mount antibody responses to a specific antigen in suckler calves.
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Shouldice, Stephen R., Robert J. Skene, Douglas R. Dougan, Gyorgy Snell, Duncan E. McRee, Anthony B. Schryvers, and Leslie W. Tari. "Structural Basis for Iron Binding and Release by a Novel Class of Periplasmic Iron-Binding Proteins Found in Gram-Negative Pathogens." Journal of Bacteriology 186, no. 12 (June 15, 2004): 3903–10. http://dx.doi.org/10.1128/jb.186.12.3903-3910.2004.
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ABSTRACT We have determined the 1.35- and 1.45-Å structures, respectively, of closed and open iron-loaded forms of Mannheimia haemolytica ferric ion-binding protein A. M. haemolytica is the causative agent in the economically important and fatal disease of cattle termed shipping fever. The periplasmic iron-binding protein of this gram-negative bacterium, which has homologous counterparts in many other pathogenic species, performs a key role in iron acquisition from mammalian host serum iron transport proteins and is essential for the survival of the pathogen within the host. The ferric (Fe3+) ion in the closed structure is bound by a novel asymmetric constellation of four ligands, including a synergistic carbonate anion. The open structure is ligated by three tyrosyl residues and a dynamically disordered solvent-exposed anion. Our results clearly implicate the synergistic anion as the primary mediator of global protein conformation and provide detailed insights into the molecular mechanisms of iron binding and release in the periplasm.
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Ayalew, Sahlu, Anthony W. Confer, and Emily R. Blackwood. "Characterization of Immunodominant and Potentially Protective Epitopes of Mannheimia haemolytica Serotype 1 Outer Membrane Lipoprotein PlpE." Infection and Immunity 72, no. 12 (December 2004): 7265–74. http://dx.doi.org/10.1128/iai.72.12.7265-7274.2004.
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ABSTRACT Mannheimia haemolytica serotype 1 (S1) is the most common bacterial isolate found in shipping fever pneumonia in beef cattle. Currently used vaccines against M. haemolytica do not provide complete protection against the disease. Research with M. haemolytica outer membrane proteins (OMPs) has shown that antibodies to one particular OMP from S1, PlpE, may be important in immunity. In a recently published work, members of our laboratory showed that recombinant PlpE (rPlpE) is highly immunogenic when injected subcutaneously into cattle and that the acquired immunity markedly enhanced resistance to experimental challenge (A. W. Confer, S. Ayalew, R. J. Panciera, M. Montelongo, L. C. Whitworth, and J. D. Hammer, Vaccine 21:2821-2829, 2003). The objective of this work was to identify epitopes of PlpE that are responsible for inducing the immune response. Western blot analysis of a series of rPlpE with nested deletions on both termini with bovine anti-PlpE hyperimmune sera showed that the immunodominant region is located close to the N terminus of PlpE. Fine epitope mapping, in which an array of overlapping 13-mer synthetic peptides attached to a derivatized cellulose membrane was probed with various affinity-purified anti-PlpE antibodies, identified eight highly reactive regions, of which region 2 (R2) was identified as the specific epitope. The R2 region is comprised of eight imperfect repeats of a hexapeptide (QAQNAP) and is located between residues 26 and 76. Complement-mediated bactericidal activity of affinity-purified anti-PlpE bovine antibodies confirmed that antibodies directed against the R2 region are effective in killing M. haemolytica.
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Schubach, Kelsey, Reinaldo F. Cooke, Alice Brandão, Thiago Schumaher, Osvaldo Souza, David Bohnert, and Rodrigo Marques. "105 Altering the time of vaccination against respiratory pathogens enhanced antibody response and health of feedlot cattle." Journal of Animal Science 97, Supplement_1 (July 2019): 39–40. http://dx.doi.org/10.1093/jas/skz053.089.
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Abstract Angus × Hereford calves (n = 159; 87 heifers and 72 steers) were ranked by sex, body weight (BW), and age, and assigned to 1 of 3 vaccination schemes against the bovine respiratory disease (BRD) complex: 1) vaccination at weaning (d 0) and booster at feedyard entry (d 30; CON, n = 53), 2) vaccination 15 d before weaning (d -15) and booster 15 d before feedyard entry (d 15; EARLY, n = 53), and 3) vaccination 15 d after weaning (d 15) and booster 15 d after feedyard entry (d 45; DELAYED, n = 53). Calves were maintained on pasture from d -15 to 30, transported (d 30) for 480 km to a commercial growing yard, and moved (d 180) to an adjacent finishing lot where they remained until slaughter (d 306). Calves were assessed for BRD signs daily from d 0 to 306 according to the DART system. Blood samples were collected and BW recorded on d -15, 0, 15, 30, 45, 60, 75, and 180. Hot carcass weight was recorded upon slaughter, and carcass quality assessed after a 24-h chill. No treatment effects were detected (P ≥ 0.49) for BW gain and carcass traits (P ≥ 0.32). Incidence of BRD (d 0 to 306) was lessened (P < 0.01) in EARLY vs. CON and DELAYED, and similar (P = 0.17) between CON and DELAYED. Treatment × day interactions were detected (P ≤ 0.02) for serum antibody titers against bovine herpesvirus-1, bovine viral diarrhea virus-1, parainfluenza3, and bovine respiratory syncytial virus, which were greater (P ≤ 0.05) in EARLY vs. CON and DELAYED upon feedyard entry. Hence, anticipating initial and booster vaccination against respiratory pathogens to provide both doses prior to shipping appears to be a valid strategy to enhance cattle health responses and mitigate BRD in feedyards.
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Pandher, Karamjeet, Anthony W. Confer, and George L. Murphy. "Genetic and Immunologic Analyses of PlpE, a Lipoprotein Important in Complement-Mediated Killing of Pasteurella haemolytica Serotype 1." Infection and Immunity 66, no. 12 (December 1, 1998): 5613–19. http://dx.doi.org/10.1128/iai.66.12.5613-5619.1998.
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ABSTRACT Pasteurella haemolytica serotype 1 is the bacterium most commonly associated with bovine shipping fever. The presence of antibodies against P. haemolytica outer membrane proteins (OMPs) correlates statistically with resistance to experimentalP. haemolytica challenge in cattle. Until now, specificP. haemolytica OMPs which elicit antibodies that function in host defense mechanisms have not been identified. In this study, we have cloned and sequenced the gene encoding one such protein, PlpE. Analysis of the deduced amino acid sequence revealed that PlpE is a lipoprotein and that it is similar to an Actinobacillus pleuropneumoniae lipoprotein, OmlA. Affinity-purified, anti-PlpE antibodies recognize a protein in all serotypes of P. haemolytica except serotype 11. We found that intact P. haemolytica and recombinant E. coli expressing PlpE are capable of absorbing anti-PlpE antibodies from bovine immune serum, indicating that PlpE is surface exposed in P. haemolyticaand assumes a similar surface-exposed conformation in E. coli. In complement-mediated killing assays, we observed a significant reduction in killing of P. haemolytica when bovine immune serum that was depleted of anti-PlpE antibodies was used as the source of antibody. Our data suggest that PlpE is surface exposed and immunogenic in cattle and that antibodies against PlpE contribute to host defense against P. haemolytica.
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Starr, Amanda E., Tonima Dan, Kanwal Minhas, Patricia E. Shewen, and Brenda L. Coomber. "Potential Involvement of Gelatinases and Their Inhibitors in Mannheimia haemolytica Pneumonia in Cattle." Infection and Immunity 72, no. 8 (August 2004): 4393–400. http://dx.doi.org/10.1128/iai.72.8.4393-4400.2004.
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ABSTRACT Mannheimia haemolytica infection of the lower respiratory tract of cattle results in a bronchofibrinous pneumonia characterized by massive cellular influx and lung tissue remodeling and scarring. Since altered levels of gelatinases and their inhibitors have been detected in a variety of inflammatory conditions and are associated with tissue remodeling, we examined the presence of gelatinases in lesional and nonlesional lung tissue obtained from calves experimentally infected with M. haemolytica. Lesional tissue had elevated levels of progelatinase A and B and active gelatinase A and B when compared with nonlesional tissue obtained from the same lung lobe. In vitro, M. haemolytica products stimulated production of gelatinase B, but not its activation, by bovine monocytes. Alveolar macrophages showed constitutive production of gelatinase B but no change in response to M. haemolytica products. Bovine neutrophils exposed to M. haemolytica products also released gelatinase B, and there was a significant increase in the activated form of this enzyme. These effects were virtually identical when recombinant O-sialoglycoprotease was used to stimulate these cells. M. haemolytica products also enhanced the expression by bovine monocytes and alveolar macrophages of the tissue inhibitor of metalloproteinase 1. Our results provide evidence that matrix metalloproteinases are activated in lung lesions from cattle with shipping fever and that M. haemolytica virulence products induce production, release, and especially activation of gelatinase B by bovine inflammatory cells in vitro.
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Sun, Yude, Kenneth D. Clinkenbeard, Laura A. Cudd, Cyril R. Clarke, and Patricia A. Clinkenbeard. "Correlation of Pasteurella haemolytica Leukotoxin Binding with Susceptibility to Intoxication of Lymphoid Cells from Various Species." Infection and Immunity 67, no. 12 (December 1, 1999): 6264–69. http://dx.doi.org/10.1128/iai.67.12.6264-6269.1999.
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ABSTRACT Pasteurella haemolytica, the causative agent of shipping fever pneumonia in cattle, produces a leukotoxin (LKT) which lyses ruminant leukocytes with high efficiency but is reputed to not affect leukocytes from nonruminant species. In this study, we tested the supposition that LKT binding correlates positively with susceptibility to intoxication of susceptible isolated bovine lymphocytes and lymphoma tissue culture cells (BL3 cells) and negatively with reputed nonsusceptible equine, porcine, and canine lymphocytes and human lymphoid tissue culture cells (Raji cells). Bovine lymphocytes and BL3 cells were highly susceptible to LKT intoxication, exhibiting both substantial increase in intracellular Ca2+ concentration and marked leukolysis. Exposure of reputed LKT-nonsusceptible porcine lymphocytes and Raji cells to LKT caused a slightly increased intracellular Ca2+concentration but no leukolysis. No LKT effect was detected for equine and canine lymphocytes. LKT bound to lymphoid cells from all species tested. Intact 102-kDa LKT was recovered from exposed isolated lymphoid cell membranes. Pro-LKT acylation was not required for LKT binding to BL3 cells. LKT binding was rapid, with maximal binding occurring by 3 min, and was proportional to the LKT concentration in the range 0.04 to 4.0 μg/ml. For this LKT concentration range, BL3 cells bound more LKT than did porcine lymphocytes or Raji cells, suggesting that LKT binds to BL3 cells with higher affinity than to porcine lymphocytes or Raji cells. Above 4.0 μg/ml, LKT demonstrated saturable binding to BL3 cells. Neutralizing anti-LKT monoclonal antibody (MAb) MM601 diminished LKT binding to BL3 by 36% while decreasing leukolysis by 81%. In contrast, MM601 did not diminish LKT binding to Raji cells. Pretreatment of target cells with 120 μg of protease K per ml diminished LKT binding to BL3 cells by 75%, with only a 25% decrease in leukolysis. However, pretreatment with 150 μg of protease K per ml abolished the remaining 25% of LKT binding and 75% leukolysis. Therefore, P. haemolytica LKT binds rapidly to susceptible and to reputed nonsusceptible lymphoid cells. LKT binding resulting in species-specific leukolysis was characterized by high affinity, inhibition by MAb MM601, and relative resistance to protease K pretreatment of lymphoid cells. Two types of LKT binding to lymphoid cells are proposed. High-affinity binding leads to efficient leukolysis. In some lymphoid cells from reputed LKT-nonsusceptible species, low-affinity LKT binding may cause a low-efficiency increase in the intracellular Ca2+ concentration without leading to leukolysis.
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Chitko-McKown, Carol G., Gary L. Bennett, Larry A. Kuehn, Keith D. DeDonder, Michael D. Apley, Gregory P. Harhay, Michael L. Clawson, et al. "Cytokine and Haptoglobin Profiles From Shipping Through Sickness and Recovery in Metaphylaxis- or Un-Treated Cattle." Frontiers in Veterinary Science 8 (March 19, 2021). http://dx.doi.org/10.3389/fvets.2021.611927.
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Fifty-six head of cattle, 28 animals with bovine respiratory disease complex (BRDC), and 28 healthy animals that were matched by treatment, sale barn of origin, day, and interactions among these variables, were identified from a population of 180 animals (60 each purchased at three sale barns located in Missouri, Tennessee, and Kentucky) enrolled in a study comparing animals receiving metaphylaxis to saline-treated controls. Cattle were transported to a feedlot in KS and assigned to treatment group. Blood samples were collected at Day 0 (at sale barn), Day 1, Day 9, and Day 28 (at KS feedlot), and transported to the US Meat Animal Research Center in Clay Center, NE where plasma was harvested and stored at −80°C until assayed for the cytokines IFN-γ, IL-1β, IL-6, and TNF-α, and the acute stress protein haptoglobin (HPT). Our objectives were to determine if cytokine and haptoglobin profiles differed between control and metaphylaxis treatment groups over time, and if profiles differed between animals presenting with BRDC and those that remained healthy. There was no difference between the treated animals and their non-treated counterparts for any of the analytes measured. Sale barn of origin tended to affect TNF-α concentration. Differences for all analytes changed over days, and on specific days was associated with state of origin and treatment. The Treatment by Day by Case interaction was significant for HPT. The analyte most associated with BRDC was HPT on D9, possibly indicating that many of the cattle were not exposed to respiratory pathogens prior to entering the feedlot.
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Vlasova, Anastasia N., and Linda J. Saif. "Bovine Coronavirus and the Associated Diseases." Frontiers in Veterinary Science 8 (March 31, 2021). http://dx.doi.org/10.3389/fvets.2021.643220.
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Coronaviruses (CoVs) possess the largest and most complex RNA genome (up to 32 kb) that encodes for 16 non-structural proteins regulating RNA synthesis and modification. Coronaviruses are known to infect a wide range of mammalian and avian species causing remarkably diverse disease syndromes. Variable tissue tropism and the ability to easily cross interspecies barriers are the well-known characteristics of certain CoVs. The 21st century epidemics of severe acute respiratory CoV (SARS-CoV), Middle East respiratory CoV and the ongoing SARS-CoV-2 pandemic further highlight these characteristics and emphasize the relevance of CoVs to the global public health. Bovine CoVs (BCoVs) are betacoronaviruses associated with neonatal calf diarrhea, and with winter dysentery and shipping fever in older cattle. Of interest, no distinct genetic or antigenic markers have been identified in BCoVs associated with these distinct clinical syndromes. In contrast, like other CoVs, BCoVs exist as quasispecies. Besides cattle, BCoVs and bovine-like CoVs were identified in various domestic and wild ruminant species (water buffalo, sheep, goat, dromedary camel, llama, alpaca, deer, wild cattle, antelopes, giraffes, and wild goats), dogs and humans. Surprisingly, bovine-like CoVs also cannot be reliably distinguished from BCoVs using comparative genomics. Additionally, there are historical examples of zoonotic transmission of BCoVs. This article will discuss BCoV pathogenesis, epidemiology, interspecies transmission, immune responses, vaccines, and diagnostics.
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"Vaccine again shipping fever in cattle; contains purified Pasteurella haemolytica native or recombinant antigen of mol. wt. 105 000; monoclonal antibody production for pneumonic pasteurellosis disease diagnosis in cattle." Vaccine 9, no. 7 (July 1991): 525. http://dx.doi.org/10.1016/0264-410x(91)90042-5.
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Carrisoza-Urbina, Jacob, Estela Flores-Velázquez, José A. Gutiérrez-Reyes, and Noé Orlando Juárez-López. "Assessment of the degree of concordance between the results of histopathological examination and bacterial culture in the diagnosis of bovine tuberculosis in Mexico." Veterinaria México OA 2, no. 3 (October 26, 2015). http://dx.doi.org/10.21753/vmoa.2.3.348.
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Bovine tuberculosis is a complex disease that is difficult to diagnose, control and eradicate and negatively impacts many farms. The objective of this study was to assess the degree of concordance between the results of histopathological examination and bacterial culture in the diagnosis of bovine tuberculosis lesions obtained in the laboratories certified by the Secretaría de Agricultura, Ganadería, Desarrollo Rural, Pesca y Alimentación (Ministry of Agriculture, Animal Production, Rural Development, Fisheries and Feeding) at the national level between January 2009 and December 2012 in Mexico. Tissue samples (10,818) from regular slaughter cattle that did not have tuberculin tests but had lesions suspected of having been caused by tuberculosis were sent to 10 authorized laboratories. Using Cohen’s kappa to measure the reliability of the diagnosis, a general concordance was obtained between the histopathological examination and bacterial culture results with a kappa of 0.634 and a 95% (0.618 – 0.650) confidence interval (CI), which shows good concordance between the two techniques at the national level. The laboratory in Chihuahua had the highest kappa [k=0.784, 95% CI (0.754–0.814)] and the laboratory of the La Laguna Region in the state of Coahuila had a low value of global concordance [k= 0.334, 95% CI (0.257–0.412)]. The number of positive samples in bacterial culture was low in Tamaulipas (21 samples), Sonora (41 samples), and Yucatán (45 samples) because tuberculosis prevalence in those states is ≤ 0.04%. The number of positive samples in bacterial culture was low in Tamaulipas (21 samples), Sonora (41 samples), and Yucatán (45 samples) because tuberculosis prevalence in those states is ≤ 0.04%. The reason for the disagreement between the two tests among some laboratories includes factors such as a lack of economic resources, infrastructure or personnel training. Correct sampling procedures, storage facilities, and shipping and sample processes are important in optimizing the bacteriological and histopathological results and obtaining correct diagnoses and differential diagnoses of bovine tuberculosis.