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      Detecção molecular de Brucella canis em cães do Município de Cuiabá, Estado de Mato Grosso Translated title: Molecular detection of Brucella canis in dogs of Cuiabá city, Mato Grosso State

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          Abstract

          Este estudo teve como objetivo investigar a ocorrência da brucelose causada por Brucella canis em cães no município de Cuiabá, MT, e os possíveis fatores de risco associados durante o período de 2007 a 2008. Foram analisadas 327 amostras baseadas numa amostragem aleatória simples, abrangendo os quatro distritos do município. A ocorrência da B. canis foi de 24,1% (I.C. 95%: 19,7 - 29,0%). A análise estatística dos sinais clínicos demonstrou associação de conjuntivite e ceratite com a positividade por B. canis, com um valor de odds ratio de 4,72 (I.C.95%=1,30-17,76) e Exato de Fisher de 0,0103; e 16,69 (I.C.95%=1,86-385,55) e Exato de Fisher de 0,0036, respectivamente. Os resultados obtidos neste estudo demonstraram a ocorrência da B. canis no município de Cuiabá e sugerem novas pesquisas e monitoramento, além de propor, como diagnóstico molecular para B. canis, a técnica de PCR.

          Translated abstract

          This study aimed to investigate the occurrence of brucellosis caused by Brucella canis in dogs in Cuiabá, State of Mato Grosso, and possible risk factors associated during the period of 2007 to 2008. Three hundred twenty seven samples were analized based on simple random sampling, covering the 04(four) districts of the municipality. The occurrence of B. canis was 24.1% (95% CI: 19.7-29.0%). The statiscal analysis showed association of conjunctivitis and keratitis with the positivity of B. canis, with an odds ratio of 4.72(95% CI=1.30-17.76) and 0.0103 for Fisher's Exact, and 16.69(95% CI=1.86-385.55) and 0.0036 for Fisher's Exact, respectively. The results of this study demonstrate the occurrence of B. canis in this city of Cuiabá, and suggest and new research and monitoring and proposes a molecular diagnostics to B. canis, the PCR techinique.

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          Biostatistical Analysis

          Designed for one/two-semester, junior/graduate-level courses in Biostatistics, Biometry, Quantitative Biology, or Statistics, the latest edition of this best-selling biostatistics text is both comprehensive and easy to read. It provides a broad and practical overview of the statistical analysis methods used by researchers to collect, summarize, analyze, and draw conclusions from biological research data. The Fourth Edition can serve as either an introduction to the discipline for beginning students or a comprehensive procedural reference for today's practitioners.
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            PCR as a diagnostic tool for brucellosis.

            Numerous PCR-based assays have been developed for the identification of Brucella to improve diagnostic capabilities. Collectively, the repertoire of assays addresses several aspects of the diagnostic process. For some purposes, the simple identification of Brucella is adequate (e.g. diagnosis of human brucellosis or contamination of food products). In these cases, a genus-specific PCR assay is sufficient. Genus-specific assays tend to be simple, robust, and somewhat permissive of environmental influences. The main genetic targets utilized for these applications are the Brucella BCSP31 gene and the 16S-23S rRNA operon. Other instances require identification of the Brucella species involved. For example, most government-sponsored brucellosis eradication programs include regulations that stipulate a species-specific response. For epidemiological trace back, strain-specific identification is helpful. Typically, differential PCR-based assays tend to be more complex and consequently more difficult to perform. Several strategies have been explored to differentiate among Brucella species and strains, including locus specific multiplexing (e.g. AMOS-PCR based on IS711), PCR-RFLP (e.g. the omp2 locus), arbitrary-primed PCR, and ERIC-PCR to name a few. This paper reviews some of the major advancements in molecular diagnostics for Brucella including the development of procedures designed for the direct analysis of a variety of clinical samples. While the progress to date is impressive, there is still room for improvement. Copyright 2002 Elsevier Science B.V.
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              Comparison of agar gel immunodiffusion test, rapid slide agglutination test, microbiological culture and PCR for the diagnosis of canine brucellosis.

              The performance of the rapid slide agglutination test, with and without 2-mercaptoethanol (RSAT and 2ME-RSAT) and agar gel immunodiffusion test (AGID) was evaluated for the diagnosis of brucellosis in naturally infected dogs. The microbiological culture, PCR and clinical parameters were used as reference. A total of 167 dogs were clinically examined and tested by blood culture, culture of semen/vaginal swab and PCR in blood and semen/vaginal swab. According to the results observed the 167 dogs were divided into three groups: Brucella canis infected dogs (Group 1), B. canis non-infected dogs (Group 2) and dogs with suspected brucellosis (Group 3). The dogs were then tested by RSAT, 2ME-RSAT and AGID. Groups 1 and 2 were used to calculate the diagnostic sensitivity and specificity of the serological tests and the results observed in Group 3 were also discussed. The diagnostic sensitivity of RSAT, 2ME-RSAT and AGID was respectively 70.58%, 31.76%, and 52.94%. The diagnostic specificity of RSAT, 2ME-RSAT and AGID was respectively 83.34%, 100%, and 100%. In dogs with suspected brucellosis 15% were RSAT positive, none was 2ME-RSAT positive and 5% were AGID positive. Although the serological tests are the most commonly used methods for brucellosis diagnosis, a significant proportion of false-negative results were observed highlighting the importance of the direct methods of diagnosis, like blood culture and PCR to improve the diagnosis of canine brucellosis.
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                Author and article information

                Journal
                cr
                Ciência Rural
                Cienc. Rural
                Universidade Federal de Santa Maria (Santa Maria, RS, Brazil )
                0103-8478
                1678-4596
                June 2012
                : 42
                : 6
                : 1051-1056
                Affiliations
                [02] Cuiabá MT orgnameUFMT Brasil
                [01] Cuiabá MT orgnameUniversidade Federal de Mato Grosso (UFMT) Brasil valdutra@ 123456ufmt.br
                Article
                S0103-84782012000600016 S0103-8478(12)04200600016
                f8dd807d-3d0d-4527-91c7-cfda98cf4d8d

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 23 August 2011
                : 08 February 2012
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 33, Pages: 6
                Product

                SciELO Brazil

                Categories
                Microbiologia

                brucellosis,PCR,Brucella canis,dogs,Cuiabá,brucelose,cães
                brucellosis, PCR, Brucella canis, dogs, Cuiabá, brucelose, cães

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