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  • 1
    In: Veterinary Microbiology, Elsevier BV, Vol. 170, No. 3-4 ( 2014-06), p. 246-257
    Type of Medium: Online Resource
    ISSN: 0378-1135
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2014
    detail.hit.zdb_id: 1498996-7
    SSG: 22
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  • 2
    In: Journal of Veterinary Diagnostic Investigation, SAGE Publications, Vol. 23, No. 4 ( 2011-07), p. 817-820
    Abstract: A 7.5-year-old raccoon dog ( Nyctereutes procyonoides) from the Henry Doorly Zoo (Omaha, Nebraska) presented to the veterinary hospital for lethargy and weight loss. On physical examination, splenomegaly and hepatomegaly were noted on palpation and were confirmed by radiographic evaluation. Radiography also demonstrated a mass in the cranial mediastinum. A complete blood cell count revealed marked leukocytosis (115,200 cells/µl), with a predominance of lymphoid cells. The animal was euthanized due to a poor prognosis. Necropsy revealed splenomegaly, hepatomegaly, and a large multiloculated mass in the cranial mediastinum. The histologic and immunohistochemical diagnosis was multicentric T-cell lymphoma with a leukemic phase.
    Type of Medium: Online Resource
    ISSN: 1040-6387 , 1943-4936
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2011
    detail.hit.zdb_id: 2265211-5
    SSG: 22
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  • 3
    In: Veterinary Research, Springer Science and Business Media LLC, Vol. 45, No. 1 ( 2014), p. 38-
    Type of Medium: Online Resource
    ISSN: 1297-9716
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2014
    detail.hit.zdb_id: 2012391-7
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  • 4
    Online Resource
    Online Resource
    Frontiers Media SA ; 2023
    In:  Frontiers in Veterinary Science Vol. 10 ( 2023-3-30)
    In: Frontiers in Veterinary Science, Frontiers Media SA, Vol. 10 ( 2023-3-30)
    Abstract: Tritrichomonas foetus (TF) is a significant reproductive pathogen of cattle, and sample collection, handling, transport, and testing are significant hurdles to surveillance programs. Recent methods have been developed that allow for the direct detection of TF using a reverse transcription real-time PCR (direct RT-qPCR) approach. To evaluate these methods, a comparative analysis was conducted to assess the technical performance of this assay with a commercially available real-time PCR (qPCR) assay. In addition, the evaluation of two types of collection media (PBS and TF transport tube) was conducted that evaluated sample stability from 0 to 3 days when stored at 4°C or 25°C. Extended incubation times for PBS media were also evaluated (5, 7, and 14 days) at both refrigeration and frozen temperatures to evaluate the effect of extended transport time on samples. Limits of detection (LODs), dynamic range, and RNA stability were assessed using lab-cultured TF spiked into samples of normal bovine smegma collected in PBS or TF transport media, and performance was assessed on field samples collected in parallel. 100% agreement was found between direct RT-qPCR and qPCR at 10 parasites/extraction and a LOD of 1 parasite/extraction. Differences in detection were not observed in either collection media when incubated at either temperatures for up to 3 days of incubation. In addition, the extended incubation experiments indicate that samples containing 10 parasites/extraction can be detected at 4°C for 5 days with a mean Cq 26.34 (95% CI: 23.11–29.58) and detected at −20°C for 7 or 14 days, with a mean Cq 29.55 (95% CI: 27.73–31.37). A significant decrease in detectable RNA was observed in samples containing & lt;10 parasites/extraction at −20°C for 14 days, which should be considered for long-term storage. In summary, direct RT-qPCR was found to be equivalent or superior to qPCR and PBS was not significantly different from TF transport media. The findings of the current study allows for more flexibility during sample collection and transport and ultimately enhancement of TF surveillance programs.
    Type of Medium: Online Resource
    ISSN: 2297-1769
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2023
    detail.hit.zdb_id: 2834243-4
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  • 5
    In: JMM Case Reports, Microbiology Society, Vol. 2, No. 5 ( 2015-10-09)
    Type of Medium: Online Resource
    ISSN: 2053-3721
    Language: English
    Publisher: Microbiology Society
    Publication Date: 2015
    detail.hit.zdb_id: 2755673-6
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  • 6
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 1999
    In:  Viral Immunology Vol. 12, No. 4 ( 1999-01), p. 323-334
    In: Viral Immunology, Mary Ann Liebert Inc, Vol. 12, No. 4 ( 1999-01), p. 323-334
    Type of Medium: Online Resource
    ISSN: 0882-8245 , 1557-8976
    RVK:
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 1999
    detail.hit.zdb_id: 2030616-7
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  • 7
    Online Resource
    Online Resource
    Texas A&M University Libraries ; 2019
    In:  The Bovine Practitioner ( 2019-08-15), p. 13-22
    In: The Bovine Practitioner, Texas A&M University Libraries, ( 2019-08-15), p. 13-22
    Abstract: Elements of a bovine viral diarrhea virus (BVDV) biosecurity program, associated costs and benefits, and criteria veterinarians and producers can use in considering whether to adopt a program are described in this report. Protection against BVDV infections includes proper immunization, identification and elimination of persistently infected (PI) carrier cattle, and prevention of exposure of cattle at risk to BVDV. The decision to implement a BVDV biosecurity program must be based on a herd-by-herd cost-benefit analysis. Costs include diagnostic testing as well as costs imposed by constraints on production practices, which are necessary to implement the program. Benefits include reduced disease loss, potential added value of replacement breeding animals which can be marketed as test-negative for PI infection, and pregnant females at low risk of carrying a PI fetus. Various herd-level diagnostic strategies have been devised to screen herds for the presence ofBVDV, identify and eliminate PI carrier cattle, or help prevent new exposure of the herd to BVDV. No universally applicable protocol exists for herd level BVDV biosecurity. The specific biosecurity methods used in each herd depend on the type of livestock production system involved. Important variables to consider are the number of animals in the herd, livestock concentration, distribution of animal groups, and desired level of biosecurity assurance. When BVDV virus is known to exist in a herd, control of new infections must take into account the possible presence of PI animals. A single PI animal can serve as the source of virus for a herd, and a stringent herd testing program may be required to identify and eliminate PI animals. Producers must understand the risks of re-exposure occurring in a BVDV-free herd and the importance of continuous management to prevent contact with cattle from other herds. In BVDV-free herds, it is essential to annually test and confirm the BVDV PI-free status of all calves born. Purchased animals should be isolated and tested before being added to the herd to avoid introduction of transiently infected animals. It is strongly recommended that bred heifers from outside sources not be added to the BVDV-free herd. Purchasing tested, non-pregnant replacement heifers is less risky than buying tested pregnant females. If tested, pregnant cattle are purchased, then the offspring must also be tested to confirm their BVDV PI-free status before introduction into the herd.
    Type of Medium: Online Resource
    ISSN: 0524-1685
    Language: Unknown
    Publisher: Texas A&M University Libraries
    Publication Date: 2019
    detail.hit.zdb_id: 3112158-5
    SSG: 22
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  • 8
    In: The Bovine Practitioner, Texas A&M University Libraries, ( 1997-01-01), p. 32-38
    Abstract: The potential synergistic effects of BVDV and BRSV infections were investigated. Single virus infections often produce mild, if any, clinical disease in controlled animal challenge studies. The multi-etiologic nature of bovine respiratory disease is well-documented, and the potential effects of dual infection more closely reproduces natural disease and the significance of pathogenic viruses. This is important in designing vaccination programs for disease control. Fourteen Hereford beef calves weighing approximately 205 kilograms were obtained from a ranch in western Nebraska. The calves were seronegative to IBR, BVD, PI3, and BRSV, and were confirmed to be free of persistent BVD infection through repeated negative virus isolation. Random assignment to form treatment groups allotted four calves to a BVD challenge alone, four calves to a BRSV challenge alone, four calves to dual BVD, BRSV challenge, and two calves to a negative control group. Evaluation methods included pre- mortem clinical scoring, hematology, and virus isolation. Euthanatized calves were evaluated by virus isolation, gross pathologic, and histopathologic evaluation. Severity of clinical signs (depression, serous to mucopurulent nasal discharge, and dyspnea) and extent of lung injury was greater in calves inoculated with dual BRSV/ BVDV than in calves inoculated with either virus alone. Potentiation of BVDV infection of the digestive tract by BRSV was indicated by augmentation of clinical diarrhea in calves dually-infected with BRSV and BVDV compared to calves infected only with BVDV. Gross and histopathologic lesions correlated to pre-mortem clinical observations. BVDV and BRSV potentiate each other in dual virus infection, causing more severe clinical signs and lesions than in infection with either virus alone. This more closely mimics natural infections, and better establishes the clinical significance of these pathogens than single virus controlled challenges studies.
    Type of Medium: Online Resource
    ISSN: 0524-1685
    Language: Unknown
    Publisher: Texas A&M University Libraries
    Publication Date: 1997
    detail.hit.zdb_id: 3112158-5
    SSG: 22
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  • 9
    Online Resource
    Online Resource
    American Veterinary Medical Association (AVMA) ; 2003
    In:  American Journal of Veterinary Research Vol. 64, No. 4 ( 2003-04-01), p. 428-434
    In: American Journal of Veterinary Research, American Veterinary Medical Association (AVMA), Vol. 64, No. 4 ( 2003-04-01), p. 428-434
    Abstract: Objective —To evaluate persistence of bovine viral diarrhea virus (BVDV) in semen after inoculation of postpubertal bulls. Animals —Three 2-year-old bulls and five 6-month-old calves. Procedure —3 seronegative 2-year-old bulls were inoculated intranasally with BVDV. Serum and semen samples were obtained at regular intervals until 7 months after inoculation. Serum samples were tested for BVDV by use of virus isolation (VI) and reverse transcription-nested polymerase chain reaction (RTnPCR) tests. Semen samples were tested for virus by use of VI and RT-nPCR tests. Testicular biopsy specimens were obtained 7 months after inoculation and tested for BVDV by use of immunohistochemical analysis and VI and RT-nPCR tests. Semen samples collected from 1 bull immediately before and 5 and 7 months after inoculation were administered IV to seronegative calves, which were monitored for subsequent viremia and seroconversion. Results —Use of VI and RT-nPCR tests detected transient virus in serum of all bulls. The VI test detected BVDV in semen of 2 bulls for 〈 21 days after inoculation, whereas RT-nPCR assay detected BVDV until 7 months after inoculation. Virus was detected in testicular biopsy specimens of these 2 bulls by use of immunohistochemical analysis and RT-nPCR assay but could only be isolated from the biopsy specimen of 1 bull. Of the calves administered semen IV to detect infectious virus, only the recipient of semen collected 5 months after inoculation of the adult bull was viremic and seroconverted. Conclusions and Clinical Relevance —Bovine viral diarrhea virus can persist in semen of acutely infected bulls for several months after exposure. ( Am J Vet Res 2003;64:428–434)
    Type of Medium: Online Resource
    ISSN: 0002-9645
    Language: Unknown
    Publisher: American Veterinary Medical Association (AVMA)
    Publication Date: 2003
    detail.hit.zdb_id: 2056942-7
    SSG: 22
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  • 10
    Online Resource
    Online Resource
    American Veterinary Medical Association (AVMA) ; 2009
    In:  Journal of the American Veterinary Medical Association Vol. 234, No. 4 ( 2009-02-15), p. 519-529
    In: Journal of the American Veterinary Medical Association, American Veterinary Medical Association (AVMA), Vol. 234, No. 4 ( 2009-02-15), p. 519-529
    Abstract: Objective —To determine the prevalence of bovine viral diarrhea virus (BVDV)–infected alpaca herds in the United States and investigate factors associated with seropositive herd status and, subsequently, determine the proportion of animals within seropositive alpaca herds that are persistently infected (PI) carriers for BVDV, obtain information regarding previous herd exposure to BVDV, determine titers of anti-BVDV antibodies of dams, and ascertain whether individual seropositive crias had received supplemental colostrum at birth. Design —Prevalence study. Animals —63 alpaca herds with ≥ 12 registered female alpacas. Procedures —250 alpaca breeders were randomly selected from 562 eligible herds listed in the Alpaca Owner and Breeders Association membership directory and mailed a voluntary participation request. Sixty-three alpaca breeders participated in the study. From each herd, blood samples from ≥ 4 crias were tested for BVDV, BVDV RNA, and serum neutralizing antibodies against BVDV. A region of the genome of BVDV recovered from PI crias was sequenced to determine genetic homology. Results —Among the 63 herds, 16 (25.4%) had seropositive crias and 4 (6.3%) had PI crias. Infections in 3 of the 4 herds with PI crias were linked as evidence by the genetic homologies of viruses. In addition to PI crias, feeding supplemental colostrum was associated with herd seropositivity. Conclusions and Clinical Relevance —Results confirmed the importance of BVDV infections in alpacas in the United States and highlighted the importance of determining the BVDV infection status of animals before they are commingled to limit exposure of herds to BVDV infection.
    Type of Medium: Online Resource
    ISSN: 0003-1488
    Language: Unknown
    Publisher: American Veterinary Medical Association (AVMA)
    Publication Date: 2009
    detail.hit.zdb_id: 2904887-4
    SSG: 22
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