RESUMO

A cross-sectional study was conducted to determine individual cow seroprevalence of Babesia bovis in adult lactating dairy cattle of Puerto Rico (PR), to assess the associations of farm management factors on herd seroprevalence, and to document the species of ticks infesting cattle within these farms. Antibody activity against B. bovis was determined using an indirect fluorescent antibody test (IFAT). Serum samples were obtained from 2,414 adult lactating dairy cattle from 76 randomly selected commercial dairy farms. Herd seroprevalence ranged from 0 to 51% with an overall individual cow seroprevalence for B. bovis of 26%. Ticks were collected from animals on 7 (9%) of the 76 participating commercial dairy farms. All collected ticks (n = 87) were Rhipicephalus (Boophilus) microplus. Factors associated with high herd seropositivity were dairy farms with calf but not heifer raising facilities (OR = 16, 95% CI = 3.0-86), having more than 4 neighbors with cattle (OR = 17, 95% CI = 1.6-178), same producer owning more than one farm (OR = 7.2, 95% CI = 1.6-32), and use of government services to apply amitraz on cattle (OR = 5.5, 95% CI = 1.5-20).

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RESUMO

A cross-sectional study was conducted to determine individual cow seroprevalence of Anaplasma marginale in adult lactating dairy cattle of Puerto Rico (PR) and to assess the associations of farm management factors on herd seroprevalence. Antibody activity against A. marginale was determined using the MSP-5 competitive enzyme-linked immunosorbent assay. Serum samples were obtained from 2,414 adult lactating dairy cattle from 76 randomly selected commercial dairy farms. Herd seroprevalence ranged from 3 to 100% with an overall individual cow seroprevalence for A. marginale of 27.4%. Factors associated with high herd seropositivity were pasture grazing as the main feed source (OR = 6.5, 95% CI = 1.2-34), observed monkeys on the premises (OR = 13, 95% CI = 1.2-138), use of 11% permethrin (OR = 17, 95% CI = 2.2-129), farmers who attended an acaricide certification program (OR = 0.18, 95% CI = 0.04-0.74), and lack of a fly control program (OR = 5.6, 95% CI = 1.3-24).

Assuntos

RESUMO

The likelihood ratio (LR) is a measure of association that quantifies how many more times likely a particular test result is from an infected animal compared to one that is uninfected. They are ratios of conditional probabilities and cannot be interpreted at the individual animal level without information concerning pretest probabilities. Their usefulness is that they can be used to update the prior belief that the individual has the outcome of interest through a modification of Bayes' theorem. Bayesian analytic techniques can be used for the evaluation of diagnostic tests and estimation of LRs when information concerning a gold standard is not available. As an example, these techniques were applied to the estimation of LRs for a competitive ELISA (c-ELISA) for diagnosis of Brucella abortus infection in cattle and water buffalo in Trinidad.Sera from four herds of cattle (n = 391) and four herds of water buffalo (n = 381) in Trinidad were evaluated for Brucella-specific antibodies using a c-ELISA. On the basis of previous serologic (agglutination) test results in the same animals, iterative simulation modeling was used to classify animals as positive or negative for Brucella infection. LRs were calculated for six categories of the c-ELISA proportion inhibition (PI) results pooled for cattle and water buffalo and yielded the following estimations (95% probability intervals): <0.10 PI, 0.05 (0ùC0.13); 0.10ùC0.249 PI, 0.11 (0.04ùC0.20); 0.25ùC0.349 PI, 0.77 (0.23ùC1.63); 0.35-0.499 PI, 3.22 (1.39ùC6.84); 0.50ùC0.749 PI, 17.9 (6.39ùC77.4); ­í0.75 PI, 423 (129ùC­è). LRs are important for calculation of post-test probabilities and maintaining the quantitative nature of diagnostic test results.

Assuntos

RESUMO

The likelihood ratio (LR) is a measure of association that quantifies how many more times likely a particular test result is from an infected animal compared to one that is uninfected. They are ratios of conditional probabilities and cannot be interpreted at the individual animal level without information concerning pretest probabilities. Their usefulness is that they can be used to update the prior belief that the individual has the outcome of interest through a modification of Bayes' theorem. Bayesian analytic techniques can be used for the evaluation of diagnostic tests and estimation of LRs when information concerning a gold standard is not available. As an example, these techniques were applied to the estimation of LRs for a competitive ELISA (c-ELISA) for diagnosis of Brucella abortus infection in cattle and water buffalo in Trinidad. Sera from four herds of cattle (n=391) and four herds of water buffalo (n=381) in Trinidad were evaluated for Brucella-specific antibodies using a c-ELISA. On the basis of previous serologic (agglutination) test results in the same animals, iterative simulation modeling was used to classify animals as positive or negative for Brucella infection. LRs were calculated for six categories of the c-ELISA proportion inhibition (PI) results pooled for cattle and water buffalo and yielded the following estimations (95% probability intervals): <0.10 PI, 0.05 (0-0.13); 0.10-0.249 PI, 0.11 (0.04-0.20); 0.25-0.349 PI, 0.77 (0.23-1.63); 0.35-0.499 PI, 3.22 (1.39-6.84); 0.50-0.749 PI, 17.9 (6.39-77.4); > or =0.75 PI, 423 (129-infinity). LRs are important for calculation of post-test probabilities and maintaining the quantitative nature of diagnostic test results.

Assuntos

RESUMO

Thirty-two young domestic water buffalo were studied to evaluate ear-tag retention during an epidemiologic field trial. Plastic ear-tags were placed in both ears before the start of the trial, which was implemented in an extensively managed domestic water buffalo herd of approximately 1000 animals in Trinidad from 1999–2001. The presence or absence of ear-tags was recorded at the times of animal handling. The rate of ear-tag loss was modeled using a parametric survival analysis assuming an exponential rate of loss. A gamma distribution was used to estimate the amount of time that each animal would be positively identified based only on the presence or absence of one or more ear-tags. The overall median ear-tag retention was 272 days. The estimated rate of ear-tag loss was 0.0024 ear-tags lost per day. The use of ear-tags alone might not be sufficient for long-term identification of extensively managed animal populations.

Assuntos

RESUMO

Thirty-two young domestic water buffalo were studied to evaluate ear-tag retention during an epidemiologic field trial. Plastic ear-tags were placed in both ears before the start of the trial, which was implemented in an extensively managed domestic water buffalo herd of approximately 1000 animals in Trinidad from 1999-2001. The presence or absence of ear-tags was recorded at the times of animal handling. The rate of ear-tag loss was modeled using a parametric survival analysis assuming an exponential rate of loss. A gamma distribution was used to estimate the amount of time that each animal would be positively identified based only on the presence or absence of one or more ear-tags. The overall median ear-tag retention was 272 days. The estimated rate of ear-tag loss was 0.0024 ear-tags lost per day. The use of ear-tags alone might not be sufficient for long-term identification of extensively managed animal populations.

Assuntos

RESUMO

Thirty-two young domestic water buffalo were studied to evaluate ear-tag retention during an epidemiologic field trial. Plastic ear-tags were placed in both ears before the start of the trial, which was implemented in an extensively managed domestic water buffalo herd of approximately 1000 animals in Trinidad from 1999-2001. The presence or absence of ear-tags was recorded at the times of animal handling. The rate of ear-tag loss was modeled using a parametric survival analysis assuming an exponential rate of loss. A gamma distribution was used to estimate the amount of time that each animal would be positively identified based only on the presence or absence of one or more ear-tags. The overall median ear-tag retention was 272 days. The estimated rate of ear-tag loss was 0.0024 ear-tags lost per day. The use of ear-tags alone might not be sufficient for long-term identification of extensively managed animal populations.

Assuntos

RESUMO

Thirty water buffalo, obtained from a brucellosis-free farm, were used to evaluate cell-mediated immune responses and bacterial clearance in response to vaccination with Brucella abortus strain RB51 (RB51) in a dose-response study. The animals were randomly divided into five treatment groups. Groups I-V received the recommended dose (RD) of RB51 vaccine once, RD twice 4 weeks apart, double RD once, double RD twice 4 weeks apart and saline once, respectively. Cell-mediated immune response to RB51 was assessed by the histological examination of haematoxylin and eosin (H&E) stained sections of lymph nodes draining the sites of inoculation and by comparison of stimulation indices (SI) derived from gamma interferon (IFN-y)assay. A mixture of cytoplasmic proteins from B. melitensis B115 (brucellergene) was used as a specific antigenic stimulus to peripheral blood mononuclear cells (PBMC) and lymph node mononuclear cells (LNMC) up to 22 post-initial-inoculation week (PIW). Supernatants harvested at 18-24 h after the in vitro antigenic stimulus were assayed for their IFN-y content by using a commercial sandwich enzyme-linked immunosorbent assay (ELISA) kit. Clearance of RB51 was assessed by the sequential immunohistochemical examination of sections of draining lymph nodes post-inoculation. There was no observable expansion of the deep cortex of lymph nodes on H&E sections indicating poor T-cell stimulation. All group V (control) water buffalo PBMC ELISA values were negative (SI<2.2) at all PIW sampling intervals. Overall PBMC-IFN-y assay detected vaccinates from treatment groups' I-IV 67 percent (4/6), 83 percent (5/6), 33 percent (2/6) and 67 percent (4/6), respectively. LNMC IFN-y assay was unimpressive and there was a negative correlation (-0.08) between the results of PBMC and LNMC of IFN-y assay. Clearance of RB51 occurred (AU)

Assuntos

Assuntos

RESUMO

Thirty water buffalo, obtained from a brucellosis-free farm, were used to evaluate cell-mediated immune responses and bacterial clearance in response to vaccination with Brucella abortus strain RB51 (RB51) in a dose-response study. The animals were randomly divided into five treatment groups. Groups I--V received the recommended dose (RD) of RB51 vaccine once, RD twice 4 weeks apart, double RD once, double RD twice 4 weeks apart and saline once, respectively. Cell-mediated immune response to RB51 was assessed by the histological examination of haematoxylin and eosin (H&E) stained sections of lymph nodes draining the sites of inoculation and by comparison of stimulation indices (SI) derived from gamma interferon (IFN-gamma) assay. A mixture of cytoplasmic proteins from B. melitensis B115 (brucellergene) was used as a specific antigenic stimulus to peripheral blood mononuclear cells (PBMC) and lymph node mononuclear cells (LNMC) up to 22 post-initial-inoculation week (PIW). Supernatants harvested at 18-24h after the in vitro antigenic stimulus were assayed for their IFN-gamma content by using a commercial sandwich enzyme-linked immunosorbent assay (ELISA) kit. Clearance of RB51 was assessed by the sequential immunohistochemical examination of sections of draining lymph nodes post-inoculation. There was no observable expansion of the deep cortex of lymph nodes on H&E sections indicating poor T-cell stimulation. All group V (control) water buffalo PBMC ELISA values were negative (SI<2.2) at all PIW sampling intervals. Overall PBMC IFN-gamma assay detected vaccinates from treatment groups' I--IV 67% (4/6), 83% (5/6), 33% (2/6) and 67% (4/6), respectively. LNMC IFN-gamma assay was unimpressive and there was a negative correlation (--.08) between the results of PBMC and LNMC of IFN-gamma assay. Clearance of RB51 occurred between 4 and 6 PIW in treatment groups I and III and between 6 and 12 PIW in groups II and IV. RB51 was not detected in any of the control animals at sampling intervals post-inoculation.

Assuntos

RESUMO

Thirty-two young domestic water buffalo (Bubalus bubalis) were obtained from a brucellosis-free farm to determine effectiveness of RB51 vaccination for prevention of Brucella infection under natural-exposure conditions in Trinidad. Study animals (20 males and 12 females 5-20 months old) were assigned to vaccination or control groups, using a block randomization design ensuring equal sex distributions between groups. The vaccination group received commercially available RB51 at the recommended calfhood dose of (1.0-3.4)x10(10) colony-forming units (CFU) and controls received 2ml sterile saline. Vaccination did not result in positive serologic results as measured by four traditional agglutination tests: standard tube agglutination test (STAT), standard plate agglutination test (SPAT), buffered plate agglutination test (BPAT), and card agglutination. Study animals were maintained in a brucellosis-positive herd in southern Trinidad with an estimated 56% prevalence to allow for natural exposure to B. abortus, which was evaluated using STAT, SPAT, BPAT, and card tests. Animals were sampled seven times over 2 years and were classified as positive if they had persistent agglutination titers or had Brucella isolated from specimens collected at completion of the study. Five of the original 32 study animals were lost to follow-up during the field trial. Six of the 14 (43%) vaccinated animals completing the study were classified as positive for Brucella infection-as were two of the 13 (15%) control animals (P=0.21). Isolates from four vaccinates and one control were confirmed as B. abortus biovar 1.

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