scholarly journals The last outbreak of bovine tuberculosis in cattle in the CzechRepublic in 1995 was caused by Mycobacterium bovis subspecies caprae

2012 ◽  
Vol 47 (No. 9) ◽  
pp. 251-263 ◽  
Author(s):  
I. Pavlik ◽  
F. Bures ◽  
P. Janovsky ◽  
P. Pecinka ◽  
M. Bartos ◽  
...  
Keyword(s):  
Great Britain ◽  
Mycobacterium Bovis ◽  
Cervus Elaphus ◽  
Bovine Tuberculosis ◽  
Red Deer ◽  
Post Mortem ◽  
Biochemical Tests ◽  
Source Of Infection ◽  
Three Samples ◽  
Green Fodder

The last outbreak of bovine tuberculosis in cattle in the CzechRepublic was detected in 1995. Signs of diarrhoea, weight loss and occasional coughing appeared in one 14-year-old cow after giving birth for the thirteenth time. Two months after these symptoms had been observed, it had to be slaughtered and numerous tuberculous lesions were found in its lung tissue, including the pleura. Within three months after the confirmation of the infection and consecutive intra-vitam and post-mortem diagnostics, all 28 remaining head of cattle from the herd (nine cows, seven bulls, six heifers and six calves) and five pigs were slaughtered. Patho-anatomical lesions were detected in all animals indicative of tuberculosis, from which Mycobacterium bovis was cultured and identified on the basis of biochemical tests and virulence test in a guinea-pig. The culture of 33 samples of other biological material than tissues (milk and urine of cows, feeding water, scrapings from the shed, fodder and others) resulted in M. bovis being detected in three samples (scrapings from shed walls). By the spoligotyping method M. bovis subsp. caprae was found in six selected isolates originating from two cows, two heifers and two bulls. It may therefore be assumed that there was one source of infection in the herd, which was the first infected old cow. In comparison with 3 176 spoligotypes in the existing database RIVM (National Institute of Public Health and the Environment, Bilthoven, The Netherlands) and literary data it was found that this spoligotype was also found in Sweden, Belgium, Great Britain, Spain, Poland, Germany and the CzechRepublic. It was impossible to determine the source of M. bovis subsp. caprae of the first infected cow on the basis of results from database and from anamnestic data. Green fodder coming from the farmer’s pastures near a forest could be considered as a possible source of M. bovis from wild ruminants like red deer (Cervus elaphus), which was found infected with bovine tuberculosis in another district of the CzechRepublic in 1991.

scholarly journals Use of ethanol extract of Mycobacterium bovis for detection of specific antibodies in sera of farmed red deer (Cervus elaphus) with bovine tuberculosis

2013 ◽  
Vol 9 (1) ◽  
pp. 256 ◽  
Author(s):  
Ashutosh Wadhwa ◽  
Rachel E Johnson ◽  
Colin G Mackintosh ◽  
J Frank T Griffin ◽  
W Waters ◽  
...  
Keyword(s):  
Mycobacterium Bovis ◽  
Cervus Elaphus ◽  
Bovine Tuberculosis ◽  
Red Deer ◽  
Ethanol Extract ◽  
Specific Antibodies

scholarly journals Molecular epidemiology of bovine tuberculosis in the CzechRepublic and Slovakia in the period 1965–2001 studied by spoligotyping

2012 ◽  
Vol 47 (No. 7) ◽  
pp. 181-194 ◽  
Author(s):  
I. Pavlik ◽  
L. Dvorska ◽  
M. Bartos ◽  
I. Parmova ◽  
I. Melicharek ◽  
...  
Keyword(s):  
Czech Republic ◽  
Cervus Elaphus ◽  
Bovine Tuberculosis ◽  
Red Deer ◽  
Effective Control ◽  
Biochemical Tests ◽  
The Czech Republic ◽  
Hydrochoerus Hydrochaeris ◽  
The Usa ◽  
Cattle Herds

Spoligotyping was used to examine IS6110-positive DNA of 26 Mycobacterium bovis, M. bovis BCG and M. bovis subsp. caprae non-viable isolates stored up to 10 years. All of these isolates were previously identified by biochemical tests and all 17/17 tested isolates were earlier found virulent for guinea pigs. In total seven spoligotypes, designated S1–S7, were detected and compared with the spoligotypes of 3 176 isolates in the database of the National Institute of Public Health and the Environment (RIVM) in Bilthoven, the Netherlands. A Neotype M. bovis strain, isolated in 1965 in the USA and thereafter stored in The Czechoslovak National Collection of Type Cultures (My 310/87) since 1987 was of an identical spoligotype S4 with the original reference M. bovis strain from the USA. The M. bovis isolates from capybara’s (Hydrochoerus hydrochaeris) imported from Germany to the Czech Republic in 1989, as well as cattle isolates from 1966, 1991 and 1994, were of the most common type S1. Also a human isolate from 1981, a M. bovis BCG vaccine strain and clinical M. bovis BCG isolates from three children with post-vaccinal complications were of this most predominant spoligotype. e four unique spoligotypes S2, S3, S5 and S6 were identified in M. bovis isolates from cattle in the years 1965, 1996 and 1967 in the CzechRepublic, respectively, but also in isolates from farmed red deer (Cervus elaphus) from 1991 and in cattle isolates from Slovakia from the year 1992. The scarcely occurring spoligotype S7, which is typical for M. b. caprae was detected in the Czech Republic from farmed red deer (1999), cattle isolates (1966, 1991, 1995) and in a strain isolated from an 80-year-old man (1999). Several strains isolated in each of three outbreaks in cattle herds were examined. Identical spoligotypes were detected in two outbreaks and different causal agents (M. bovis of spoligotype S1 and M. b. caprae of spoligotype S7) were identified in two cows from the third outbreak. e results confirm an effective control of bovine tuberculosis in the CzechRepublic and Slovakia during 1959–1968, because previously circulating spoligotypes were successfully eradicated. e data also suggest other reservoirs of bovine tuberculosis may exist among free-living wild animals.

Importance and mitigation of the risk of spillback transmission of Mycobacterium bovis infection for eradication of bovine tuberculosis from wildlife in New Zealand

2012 ◽  
Vol 141 (7) ◽  
pp. 1394-1406 ◽  
Author(s):  
M. C. BARRON ◽  
G. NUGENT ◽  
M. L. CROSS
Keyword(s):  
New Zealand ◽  
Mycobacterium Bovis ◽  
Cervus Elaphus ◽  
Bovine Tuberculosis ◽  
Red Deer ◽  
Population Control ◽  
Generic Model ◽  
Risk Period ◽  
Wild Deer ◽  
Intensive Control

SUMMARYIntroduced brushtail possums (Trichosurus vulpecula) are wildlife maintenance hosts for Mycobacterium bovis in New Zealand, often living sympatrically with other potential hosts, including wild red deer (Cervus elaphus scoticus). Population control of possums has been predicted to eradicate tuberculosis (TB) from New Zealand wildlife; however, there is concern that long-lived M. bovis-infected deer could represent a ‘spillback’ risk for TB re-establishment (particularly when possum populations recover after cessation of intensive control). We constructed a time-, age- and sex-structured, deer/TB population generic model and simulated the outcomes of deer control on this potential spillback risk. Maintaining intensive possum control on a 5-year cycle, the predicted spillback risk period after TB eradication from possums is ∼7 years, while the probability of TB re-establishing in possums over that period is ∼6%. Additional targeted control of deer would reduce the risk period and probability of spillback; however, even with high population reductions (up to 80%) only modest decreases in risk and risk period would be achieved. We conclude that possum control alone remains the best strategy for achieving TB eradication from New Zealand habitats in which possums and wild deer are the main M. bovis hosts.

scholarly journals Lesion Distribution and Epidemiology ofMycobacterium bovisin Elk and White-Tailed Deer in South-Western Manitoba, Canada

2011 ◽  
Vol 2011 ◽  
pp. 1-11 ◽  
Author(s):  
Todd K. Shury ◽  
Doug Bergeson
Keyword(s):  
Mycobacterium Bovis ◽  
Geographic Distribution ◽  
Cervus Elaphus ◽  
Red Deer ◽  
Core Area ◽  
Age Classes ◽  
Small Core ◽  
The Core ◽  
Free Ranging ◽  
Culture Positive

Surveillance forMycobacterium bovisin free-ranging elk (Cervus elaphus) and white-tailed deer (Odocoileus virginianus) from south-western Manitoba was carried out from 1997 to 2010 to describe the lesions, epidemiology, and geographic distribution of disease. Tissues were cultured from animals killed by hunters, culled for management, blood-tested, or found opportunistically. Period prevalence in elk was approximately six times higher than deer, suggesting a significant reservoir role for elk, but that infected deer may also be involved. Prevalence was consistently higher in elk compared to deer in a small core area and prevalence declines since 2003 are likely due to a combination of management factors instituted during that time. Older age classes and animals sampled from the core area were at significantly higher risk of being culture positive. Positive elk and deer were more likely to be found through blood testing, opportunistic surveillance, and culling compared to hunting. No non-lesioned, culture-positive elk were detected in this study compared to previous studies in red deer.

scholarly journals Improvement of bovine tuberculosis diagnosis

2021 ◽  
pp. 261-265
Author(s):  
M. O. Baratov
Keyword(s):  
Red Blood Cells ◽  
Mycobacterium Bovis ◽  
Blood Cells ◽  
Bovine Tuberculosis ◽  
Intradermal Test ◽  
Mycobacterium Fortuitum ◽  
Post Mortem ◽  
Post Mortem Examination ◽  
Antibody Titers ◽  
Specific Reactions

Detection of animals with non-specific reactions to tuberculin is one of the major problems in bovine tuberculosis (TB) diagnosis. There is a need to find and improve methods for detection of the sensitization causes. This paper presents the results of comparative studies of different ways to stabilize red blood cells in order to obtain diagnosticums for indirect hemagglutination (IHA) test. The article describes the stages of red blood cells stabilization and sensitization and demonstrates the diagnostic significance of Fili stabilization method using formaldehyde as a fixative. The highest antibody titers (1:3000 and 1:4000) were received in hyperimmune sera of rabbits immunized with Mycobacterium bovis using a homologous diagnosticum. Practical importance of the sensitins homologous to the infection is shown during testing of 1,911 serum samples collected from animals of different categories (diseased; healthy and reacting to tuberculin; healthy and not reacting to tuberculin) with IHA test using diagnosticums produced from Mycobacterium bovis and Mycobacterium fortuitum. Based on the positive results of the IHA test, TB was diagnosed in 87.5% of animals originating from an infected farm during post-mortem examination. The results of the IHA test agreed with those of the intradermal tuberculin test in 37.7% of cases. Diagnostic antibody titers were found in 206 TB infected animals with no reaction to the intradermal test. However, the post-mortem examination revealed TB changes in internal organs. The obtained data suggest a possibility to use the IHA test to detect TB infected animals with non-specific reactions to tuberculin.

scholarly journals Bovine tuberculosis in one cattle herd in Ibadan in Nigeria

2012 ◽  
Vol 49 (No. 11) ◽  
pp. 406-412 ◽  
Author(s):  
S. I B Cadmus ◽  
N. N Atsanda ◽  
S. O Oni ◽  
E. E U Akang
Keyword(s):  
Mycobacterium Bovis ◽  
Bovine Tuberculosis ◽  
Molecular Typing ◽  
Human Population ◽  
Tuberculin Test ◽  
Cattle Herd ◽  
Post Mortem ◽  
Risk Of Infection ◽  
Cultural Isolation ◽  
Male Animal

Bovine tuberculosis was investigated in one private herd with 171 cattle after five cases were suspected to be tuberculous following post mortem examination. Using the intradermal comparative cervical tuberculin test 18 (10.5%) animals (ages from 2 to 12 years) were positive: 11 animals of N’dama breed and seven animals of White Fulani (i.e. Bunaji) breed; 17 female and one male animal. In all 11 randomly selected positive reactors, a spectrum of tuberculous lesions affecting the lungs, spleen, heart, liver, and the lymph nodes were observed. All the smear samples obtained were positive for acid-fast bacilli; cultural isolation confirmed the growth of mycobacteria on pyruvate-enriched Loewenstein-Jensen medium, which were identified by molecular typing to be Mycobacterium bovis. This study demonstrates widespread infection in this cattle herd and potential risk of infection for the human population with M. bovis.

Diagnosis of Mycobacterium bovis infection in livestock using gamma interferon assay and single intradermal comparative tuberculin test in Assam and Meghalaya

2017 ◽  
Author(s):  
Acheenta G. Barua ◽  
Himangshu Raj ◽  
Ashok Kumar ◽  
Chandana C. Barua ◽  
Arundhati Purkayastha ◽  
...  
Keyword(s):  
Mycobacterium Bovis ◽  
Bovine Tuberculosis ◽  
Screening Method ◽  
Tuberculin Test ◽  
Gamma Interferon ◽  
Tuberculosis Infection ◽  
Specific Detection ◽  
Biochemical Tests ◽  
Diagnostic Potential ◽  
Pcr Targeting

The present study was carried out to investigate the diagnostic potential of gamma interferon (IFN-ã) assay and single intradermal comparative tuberculin test (SICTT), including species specification of bovine tuberculosis infection in different livestock farms of Assam and Meghalaya. A total of 199 animals (cattle and buffalo) were examined for bovine tuberculosis symptoms and swab samples were cultured. Biochemical tests and PCR were used for species specification of bovine tuberculosis. Out of 199 cases examined, 33 (16.58%) showed positive for SICTT, 39 (19.59%) for IFN-ã and 35(17.59%) for PCR. Based on PCR targeting pncA region, the confirmation was done for M. Bovis. IFN-ã thus ensures a sensitive and specific detection of early bovine tuberculosis infection together with SICTT and hence may be considered as a screening method of choice.

scholarly journals Sperm Collection From Shot Red Deer Stags (Cervus Elaphus) and the Utilisation of Sperm Frozen and Subsequently Thawed

1999 ◽  
Vol 47 (2) ◽  
pp. 263-270 ◽  
Author(s):  
Z. Zomborszky ◽  
T. Zubor ◽  
J. Tóth ◽  
P. Horn
Keyword(s):  
New Zealand ◽  
Cervus Elaphus ◽  
Red Deer ◽  
Follicle Stimulating Hormone ◽  
Genetic Material ◽  
Post Mortem ◽  
Bovine Semen ◽  
Progressive Motility ◽  
Intravaginal Device ◽  
Plastic Products

Sperm samples were collected from the epididymides of 11 hunter-killed stags (Cervus elaphus hippelaphus) within 2 to 17 h post mortem in September 1991. Progressively motile spermatozoa were diluted and deep-frozen in tris-yolk extender by a procedure routinely used for bovine semen. The pre-freezing motility of spermatozoa from 6 stags was higher than 80%, while the sperm of 5 animals was found to be unsuitable for dilution. In the post-thawed sperm of six stags 40-50% of the spermatozoa showed progressive motility and the number of viable spermatozoa ranged from 8.6 to 26.7 × 106 per 0.25 ml straw. Two years later, three hinds were superovulated by the use of a progesterone-releasing intravaginal device (CIDR type G, Carter, Holt Harvey Plastic Products Group Ltd., Hamilton, New Zealand) for a period of 14 days and with follicle stimulating hormone (Folicotropin inj., Spofa, Prague). Each hind was inseminated artificially 60 h after the withdrawal of CIDR with thawed sperm injected into the uterus via the vagina. Seven days later the uteri were flushed out, as a result of which 3 early blastocysts + 1 ovum, 3 morulae + 4 ova, and 1 morula + 7 ova, respectively, were recovered from the three hinds. Deer embryos were frozen according to a glycerolbased freezing protocol. A further two years later two hinds were oestrussynchronised with CIDR type G and 300 IU PMSG (Folligon inj., Intervet, NL), and two of the thawed embryos were transplanted into two recipient hinds 7 days after heat. One of these gave birth to a normal stag fawn in June 1996. This was the first deer born in Hungary from embryo transfer. The results obtained indicate that sperm from top stags shot in the course of hunting can prove useful for the preservation of genetic material or in the development of the farmed deer system.

scholarly journals A novel multiplex-PCR for the rapid identification of Mycobacterium bovis in clinical isolates of both veterinary and human origin

2003 ◽  
Vol 130 (3) ◽  
pp. 485-490 ◽  
Author(s):  
L. COBOS-MARÍN ◽  
J. MONTES-VARGAS ◽  
S. RIVERA-GUTIERREZ ◽  
A. LICEA-NAVARRO ◽  
J. A. GONZÁLEZ-Y-MERCHAND ◽  
...  
Keyword(s):  
Multiplex Pcr ◽  
Clinical Isolate ◽  
Mycobacterium Bovis ◽  
Bovine Tuberculosis ◽  
Rapid Identification ◽  
Human Infection ◽  
Economic Losses ◽  
Human Origin ◽  
Biochemical Tests ◽  
Reliable Identification

Bovine tuberculosis is a zoonotic disease that not only causes huge economic losses but also poses an important risk for human infection. The definitive identification of a clinical isolate relies on time-consuming, highly specialized and laborious biochemical tests. We have developed a method for the rapid and reliable identification of Mycobacterium bovis and for its simultaneous differentiation from other members of the M. tuberculosis complex. Furthermore, the technique also allowed us to distinguish M. tuberculosis complex members from other Mycobacterial species. The method comprises both a single PCR and a multiplex-PCR and can be confidently applied to samples of both veterinary and human origin.

Recovery of epididymal spermatozoa from bull and red deer, stored at different times and temperatures before freezing - thawing

2012 ◽  
Vol 52 (8) ◽  
pp. 741 ◽  
Author(s):  
V. Malcotti ◽  
V. Pelufo ◽  
N. Bergamo ◽  
E. Aisen
Keyword(s):  
Cervus Elaphus ◽  
Red Deer ◽  
Treatment Time ◽  
Membrane Integrity ◽  
Sperm Chromatin ◽  
Sperm Cells ◽  
Post Mortem ◽  
Epididymal Spermatozoa ◽  
Motility Rate

In order to preserve male germoplasm, the recovery and cryopreservation of spermatozoa from the epididymides of hunted animals represents an accessible source of gametes. As a first experimental model, epididymal spermatozoa from slaughtered bulls were recovered at 30, 54, 78 and 102 h after death. The scrotal contents were stored at either 5 or 20°C. The sperm cells of each treatment (time + temperature combinations) were frozen with Triladyl (T) or Triladyl + Trehalose (TT) diluents. In order to assess sperm viability and integrity, post-thawing evaluation included individual motility, supravital stain, hyperosmotic swelling test (E+), acrosome status and sperm chromatin structure assay. Both at raw and post-refrigerated states, the sperm motility rate was higher in sperm obtained from epidydmes stored at 5°C, compared with those stored at 20°C for all collection times. Sperm collected at 102 h after death from epididymides stored at 5°C maintained a motility of 20% (120 h, raw state). When comparisons were carried out after thawing, motility was higher in the 5°C group, achieving the best results with TT diluent (7.5%) at 102 h. However, when supravital stain and E+ tests were observed, viability and membrane integrity were well preserved even at 102 h post mortem (30 and 36%, respectively, with TT diluent at 5°C). These results suggest that frozen-thawed epididymal spermatozoa could have a low motility rate while most of them remain alive. Acrosome status was not greatly affected by storage time. In a second experiment, epididymal spermatozoa from hunted red deer stags (Cervus elaphus) were recovered at 4 and 30 h after death. The scrotal contents were stored at 20°C, because that temperature is closer to field and shipment conditions. The sperm cells were frozen with TT diluent. Post-thawing evaluation included the same parameters indicated for bull spermatozoa. The assessment of spermatozoa collected at 30 hours post mortem and then subsequently frozen and thawed indicated that at this time an acceptable motility rate (35%) and viability (39.7%) were achieved. Frozen and subsequently thawed epididymal spermatozoa showed 47.9% of membrane integrity, 59.3% of acrosome integrity and 26.5% of chromatin damage, using TT diluent. A preliminary in vivo trial demonstrated that the pregnancy rate in artificially inseminated deer decreased when sperm were obtained at 30 h post mortem. According to these results, it may be concluded that storage at 5°C is better than 20°C to obtain well preserved epididymal spermatozoa from bulls, and that TT could be a useful cryoprotectant to preserve viable and fertile sperm cells after the freezing–thawing process. Before these results can be applied to assisted reproduction programs in endangered deer species, some adaptations must be developed.

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