First record of antibodies to the bluetongue virus in ewe (Ovis aries) in the state of Amazonas, Brazil / Primeiro registro de anticorpos para o vírus da língua azul em ovino (Ovis aries) no estado do Amazonas, Brasil

The objective of this work was to describe the first record of antibodies to the Bluetongue Virus (BTV) in ewe, in the state of Amazonas. The ewe, which was in twin pregnancy, gave birth on May 9, 2015, but a lamb died hours after delivery. Veterinary service was then requested by the owner, where emaciation, loss of wool, pyrexia, apathy, dyspnea, mucoid nasal secretion, facial, lingual and submandibular edema were observed. There was a visit by the Agricultural Defense Agency of the State of Amazonas to the property and blood samples were collected from the animal. The whole blood and serum were sent to the National Agricultural Laboratory, where it was possible to detect the presence of specific antibodies to BTV, through the Agar Gel Double Immunodiffusion. The ewe was submitted to a new blood collection, following the same protocols and the samples were sent to the Biological Institute of São Paulo, confirmed diagnosis. The animal in a serious clinical condition, could not resist and died in July 2015. The occurrence of an allochthonous case, in an area where vector insects occur, can trigger an endemic process in the Amazon region. With this, the epidemiological control of these occurrences is necessary, in order to avoid the spread of the disease in the country.

O objetivo do trabalho foi descrever o primeiro registro de anticorpos para o Vírus da Língua Azul (VLA) em ovino, no estado do Amazonas. A ovelha, que se encontrava em gestação gemelar, pariu no dia 9 de maio de 2015, porém um cordeiro faleceu horas após o parto. Foi então solicitado serviço veterinário por parte do proprietário, onde foi observado emaciação, perda de lã, pirexia, apatia, dispneia, secreção nasal mucoide, edema facial, lingual e submandibular. Houve visita da Agência de Defesa Agropecuária do Estado do Amazonas na propriedade e coletadas amostras de sangue do animal. O sangue total e soro foram enviados ao Laboratório Nacional Agropecuário, no qual foi possível detectar a presença de anticorpos específicos para VLA, através do teste de Imunodifusão Dupla em Gel de Ágar. A ovelha foi submetida a uma nova coleta de sangue, seguindo os mesmos protocolos e as amostras foram enviadas ao Instituto Biológico de São Paulo, confirmando diagnóstico. O animal em estado clínico grave, não resistiu e veio a óbito em julho de 2015. A ocorrência de um caso alóctone, em uma área de ocorrência de insetos vetores, pode desencadear um processo de endemia na região amazônica. Com isso, o controle epidemiológico destas ocorrências, se fazem necessários, afim de se evitar a disseminação da doença no país.

Ocorrência e fatores de risco associados à infecção por lentivírus de pequenos ruminantes no Estado de Sergipe / Occorrence and risk factors associated with small ruminant lentivirus infection in the State of Sergipe, Brazil

Os lentiviros de pequenos ruminantes (LVPR) são responsáveis por enfermidades infecciosas e multissistêmicas causadas pelo Vírus da Artrite Encefalite Caprina (CAEV) e o Vírus da Maedi-Visna (MVV), e se apresentam sob as formas clínicas: articular, mamária, respiratória e nervosa. Desta forma esse trabalho objetivou determinar a ocorrência e avaliar os fatores de risco associados à infecção por LVPR no Estado de Sergipe, Brasil. Foram coletadas amostras sanguíneas de 1200 ovinos e 675 caprinos oriundos respectivamente de 60 e 41 propriedades localizadas em 25 municípios sergipanos no período de 2011 a 2014. Os diagnósticos dos LVPR foram determinados pela técnica sorológica de Imunodifusão em Gel Ágar (IDGA) usando o kit comercial da marca Biovetech®. Os dados das variáveis associadas aos fatores de risco foram obtidos a partir de questionários aplicados aos proprietários dos rebanhos e analisados estatisticamente. As frequências absolutas e relativas foram determinadas por análise estatística descritiva e os fatores de risco por análise univariada das variáveis de interesse pelo Teste de Qui-quadrado de Pearson e Exato de Fisher, quando necessário, e em seguida submetidos à análise de regressão logística. Foi evidenciada uma soropositividade de 5,03% (34/675) em caprinos e 1,50% em ovinos com 26,82% (11/41) e 28,33% (17/60) das propriedades apresentando ao menos um animal positivo respectivamente. Na análise dos fatores de risco, não foram observadas diferenças significantes para os ovinos, enquanto que, para os caprinos, rebanhos acima de 100 animais, que pastejam em áreas comuns com outros rebanhos, em uma distância ≤500 metros entre as propriedades, que adotam medidas biotecnológicas da reprodução e não utilizam agulhas estéreis, são mais susceptíveis à infecção por LVPR. Sendo assim, conclui-se que, há a presença dos LVPR em rebanhos sergipanos, e mesmo que em baixas frequências faz-se necessário a implementação de medidas profiláticas devido a possibilidade de expansão e desenvolvimento da caprinocultura do estado, e o alto padrão genético da raça Santa Inês.(AU)

The lentiviruses of small ruminants are infectious and multisystemic diseases caused by the Caprine Arthritis Encephalitis Virus (CAEV) and the Maedi-Visna Virus (MVV), and present the clinical forms: articular, mammary, respiratory and nervous. This work aimed to determine the occurrence and to evaluate the risk factors associated with lentivirus infection of small ruminants in the State of Sergipe, Brazil. Blood samples were collected from 1200 sheep and 675 goats from 60 and 41 farms respectively, located in 25 Sergipe municipalities from 2011 to 2014. The diagnosis of small ruminant lentiviruses (LVPR) was determined by the serological technique of Immunodiffusion in Gel Agar (IDGA) using the commercial kit of the brand Biovetech®. Data from the variables associated with risk factors were obtained from questionnaires applied to the owners of the herds and analyzed statistically. Absolute and relative frequencies were determined by descriptive statistical analysis and risk factors by univariate analysis of the variables of interest by Pearson's Chi-square test and Fisher's exact test, when necessary. A logistic regression analysis was used, considering as a dependent variable for LVPR infection the reactive or non-reactive result observed in the IDGA. A seropositivity of 5.03% (34/675) was observed in goats and 1.50% in sheep with 26.82% (11/41) and 28.33% (17/60) of the properties had at least one animal positive respectively. The analysis of the risk factors, no significant differences were observed for sheep, while for goats, herds above 100 animals grazing in common areas with other herds, at a distance ≤ 500 meters between the properties, that adopt Biotechnological measures of reproduction and do not use sterile needles, are more susceptible to LVPR infection. Therefore, it´s concluded there is presence of lentiviruses of small ruminants in sergipan herds, and even if at low frequencies it is necessary to implement prophylactic measures due to the possibility of expansion and development of goat breeding of the state and the high genetic standard of the Santa Inês breed.(AU)

Investigação sorológica das lentiviroses de pequenos ruminantes nas microrregiões homogêneas do Alto Médio Canindé, Picos e Floriano, Piauí, Brasil / Serological investigation of lentiviruses of small ruminants in the microregions of Alto Médio Canindé, Picos and Floriano, Piauí state, Brazil

Lentivírus de pequenos ruminantes (LV) é o termo genérico utilizado para designar os vírus da artrite encefalite caprina e Maedi-Visna, os quais pertencem à família Retroviridae, subfamília Orthoretrovirinae, gênero Lentivirus. Tais vírus infectam caprinos e ovinos, causando enfermidades de curso lento com lesões inflamatórias, crônicas e degenerativas que podem atingir vários órgãos, provocando caquexia e morte. Os animais infectados eliminam o vírus sobretudo por meio de secreções e excreções e transmitem-no especialmente em situações de estreito contato. Não há tratamento até o momento. O controle é baseado na criação segregada, no manejo e no sacrifício dos positivos. Esse agente infeccioso já foi relatado em várias partes do mundo, sendo responsável por perdas econômicas significativas. Por o agente ter sido verificado em vários estados do Brasil e por não existirem dados soroepidemiológicos nas mesorregiões sudeste e sudoeste piauiense, esta pesquisa teve por objetivo realizar inquérito sorológico para investigar a ocorrência de anticorpos para o LV em ovinos e caprinos nas microrregiões do Alto Médio Canindé, Picos e Floriano, no Piauí. Para tanto, foram coletadas 1.280 e 1.360 amostras de soro caprino e ovino, respectivamente, oriundos de 20 municípios, distribuídos nas três microrregiões, sendo o número de amostras proporcional ao rebanho efetivo de cada município. As amostras de soro foram analisadas utilizando o teste de imunodifusão em gel de agarose (IDGA). Nenhum dos soros pesquisados reagiu positivamente, constatando-se soroprevalência nula. Ressalta-se a importância da implantação de um rigoroso programa de controle para que se possa evitar a introdução e/ou a disseminação desse agente infeccioso nessas microrregiões.(AU)

Small ruminant lentiviruses (LV) is the generic term for the caprine arthritis-encephalitis and ­­Maedi-Visna viruses, which belong to the Retroviridae family, Orthoretrovirinae subfamily, Lentivirus genus. The virus infects goats and sheep, causing slow course of disease with inflammatory, chronic and degenerative lesions, which can reach several organs, provoking cachexia and death. Infected animals eliminate the virus mainly through secretions and excretions and transmit it especially in close contact situations. There is no treatment to date. The control is based on segregated creation, management and sacrifice of the positive. This infectious agent has been reported in various parts of the world and is responsible for significant economic losses. It was verified in several states of Brazil and there are seroepidemiological data in southeast and southwest mesoregions of Piauí, Brazil. This research aimed to perform serological survey to investigate the occurrence of antibodies to LV in sheep and goats, in the regions of Alto Médio Canindé, Picos and Floriano. So, 1,280 and 1,360 serum goats and sheep samples, respectively, were collected, coming from 20 municipalities, distributed in the 3 microregions. The number of samples was proportional to the actual herd of each municipality. The samples were analyzed using the agar gel immunodiffusion test. None of the surveyed sera reacted positively, though there is a null seroprevalence. It was emphasized the importance of implementing a rigorous control program in order to prevent the introduction and spread of this infectious agent in these microregions.(AU)

Investigação sorológica das lentiviroses de pequenos ruminantes nas microrregiões homogêneas do Alto Médio Canindé, Picos e Floriano, Piauí, Brasil / Serological investigation of lentiviruses of small ruminants in the microregions of Alto Médio Canindé, Picos and Floriano, Piauí state, Brazil

Small ruminant lentiviruses (LV) is the generic term for the caprine arthritis-encephalitis and ­­Maedi-Visna viruses, which belong to the Retroviridae family, Orthoretrovirinae subfamily, Lentivirus genus. The virus infects goats and sheep, causing slow course of disease with inflammatory, chronic and degenerative lesions, which can reach several organs, provoking cachexia and death. Infected animals eliminate the virus mainly through secretions and excretions and transmit it especially in close contact situations. There is no treatment to date. The control is based on segregated creation, management and sacrifice of the positive. This infectious agent has been reported in various parts of the world and is responsible for significant economic losses. It was verified in several states of Brazil and there are seroepidemiological data in southeast and southwest mesoregions of Piauí, Brazil. This research aimed to perform serological survey to investigate the occurrence of antibodies to LV in sheep and goats, in the regions of Alto Médio Canindé, Picos and Floriano. So, 1,280 and 1,360 serum goats and sheep samples, respectively, were collected, coming from 20 municipalities, distributed in the 3 microregions. The number of samples was proportional to the actual herd of each municipality. The samples were analyzed using the agar gel immunodiffusion test. None of the surveyed sera reacted positively, though there is a null seroprevalence. It was emphasized the importance of implementing a rigorous control program in order to prevent the introduction and spread of this infectious agent in these microregions.

Lentivírus de pequenos ruminantes (LV) é o termo genérico utilizado para designar os vírus da artrite encefalite caprina e Maedi-Visna, os quais pertencem à família Retroviridae, subfamília Orthoretrovirinae, gênero Lentivirus. Tais vírus infectam caprinos e ovinos, causando enfermidades de curso lento com lesões inflamatórias, crônicas e degenerativas que podem atingir vários órgãos, provocando caquexia e morte. Os animais infectados eliminam o vírus sobretudo por meio de secreções e excreções e transmitem-no especialmente em situações de estreito contato. Não há tratamento até o momento. O controle é baseado na criação segregada, no manejo e no sacrifício dos positivos. Esse agente infeccioso já foi relatado em várias partes do mundo, sendo responsável por perdas econômicas significativas. Por o agente ter sido verificado em vários estados do Brasil e por não existirem dados soroepidemiológicos nas mesorregiões sudeste e sudoeste piauiense, esta pesquisa teve por objetivo realizar inquérito sorológico para investigar a ocorrência de anticorpos para o LV em ovinos e caprinos nas microrregiões do Alto Médio Canindé, Picos e Floriano, no Piauí. Para tanto, foram coletadas 1.280 e 1.360 amostras de soro caprino e ovino, respectivamente, oriundos de 20 municípios, distribuídos nas três microrregiões, sendo o número de amostras proporcional ao rebanho efetivo de cada município. As amostras de soro foram analisadas utilizando o teste de imunodifusão em gel de agarose (IDGA). Nenhum dos soros pesquisados reagiu positivamente, constatando-se soroprevalência nula. Ressalta-se a importância da implantação de um rigoroso programa de controle para que se possa evitar a introdução e/ou a disseminação desse agente infeccioso nessas microrregiões.

Soroprevalência de Maedi-visna em rebanhos ovinos do estado do Maranhão, Brasil / Seroprevalence of Maedi-Visna in sheep flocks State of Maranhão, Brazil

Apesar de ter sido relatada em vários estados, não há informação sobre o Vírus da Maedi Visna (MVV) no Maranhão, e com o crescimento de sua ovinocultura, aumenta o fluxo de animais de outras regiões. Com isso objetivou-se determinar a soroprevalência do MVV em rebanhos ovinos das três principais mesorregiões produtoras do estado do Maranhão, através da pesquisa das 1.495 amostras sanguíneas de ovinos, com idade superior a seis meses, pertencentes a 83 rebanhos de 23 municípios das mesorregiões Cento, Leste e Norte. O diagnóstico sorológico da infecção pelo vírus MVV foi realizado por meio do teste de imunodifusão em gel de ágar (micro-IDGA). Constatou-se uma prevalência geral de 0,7% (IC95%:0,4-1,3%) de ovinos soropositivos e prevalências nas mesorregiões Centro, Leste e Norte de 0,5% (IC95%:0,1-1,4%), 0,7% (IC95%:0,2-1,8%) e 1% (IC95%:0,3-2,4%) respectivamente. Em relação à variável sexo, não foi observada diferença significativa (P>0,05) entre machos (0,5%, IC95%:0-2,7%) e fêmeas (0,8%, IC95%:0,4-1,4%), assim como quanto a genética comparando-se ovinos de raças puras (1,5%, IC95%: 0,4-8,1%), mestiços (1%, IC95%:0,4-2,0%) e SRD (0,3%, IC95%:0,04-1,1%). A análise quanto à idade não demonstrou diferença significante (P>0,05). Conclui-se que a infecção pelo MVV está presente em ovinos das mesorregiões estudadas, sendo este o primeiro registro desta enfermidade no estado do Maranhão. Considerando a baixa prevalência, é necessário evitar a introdução e a propagação do vírus entre os rebanhos, através da exigência de testes negativos para MVV e descarte dos ovinos positivos.

Although it has been reported in several states, no information about Maedi-Visna (MV) in the state of Maranhão is available. The aim of the present study was to determine the seroprevalence of Maedi Visna Virus (MVV) in sheep flocks of the three most important sheep rearing areas from Maranhão State, Brazil. We surveyed 1.495 blood samples from sheep older than six months, of both sexes and various breeds. The samples were collected from 83 herds of 23 municipalities present in the Central, East and North regions of Maranhão. The immunodifusion agar gel (micro-AGID) performed serological diagnosis of infection MVV. The statistical analysis was performed by Fisher's test, using Epi Info. It was found an overall prevalence of MVV infection of 0,7% (CI95%:0,4-1,3%) the ovines and prevalence of 0,5% (CI95%:0,1-1,4%), 0,7% (CI95%:0,2-1,8%) e 1% (CI95%:0,3-2,4%) in the Central, East and North regions, respectively. In relation to sex, there wasn't a significant difference (P>0.05) between males (0,5,%, CI95%:0-2,7%) and females (0,8%, CI95%:0,4-1,4%), as well as in relation to genetic comparing sheep purebreds (1,5%, CI95%:0,4-8,1%), crossbred (1%, CI95%:0,4-2,0%) and SRD (0,3%, IC95%:0,04-1,1%). In relation to age wasn't observed significant difference. It has concluded that infection with MVV is present in the studied population in low prevalence. This is the first record of MVV in sheep in the State of Maranhão. Considering the low prevalence is necessary to prevent the introduction and spread of the virus between flocks by requiring negative tests for MVV and disposal of positive sheep.

Seperation and purification of daidzein by agar gel microspheres bonded β-cyclodextrin study on and its chromatographic mechanism / 中草药

Objective: Daidzein was efficiently purified by agar gel microspheres bonded β-cyclodextrin (AG-β-CD). Methods: Using agar as raw material, after emulsification, crosslinking, and bonding β-CD as functional group, AG-β-CD was synthesized for the purification of daidzein, and the purification process was determined and proved with mobile phase, flow rate, and loading capacity of microspheres. The structure of daidzein was identified by MS and NMR, AG-β-CD was chromatographically evaluated with daidzein, EGCG, and puerarin as the following tripartition such as difference of retention behavior on C18 reversed phase column chromatography, molecular simulation by autoDOCK4.0, and retention time curves on AG-β-CD with different contents of acetonitrile. Results: The main component of soybean isoflavone was daidzein (57.14%). The loading quantity of AG-β-CD was 1.33 mg/mL, flow rate was 2 BV/h, eluted by 2 BV of 20% ethanol, 1.33 BV of 40% ethanol, and 6-7 BV of 70% ethanol, the content was ≥ 95%, purity of daidzein (96.98%) was obtained with 97.86% yield. Chromatographic mechanism research showed that AG-β-CD had hydrophilic interaction chromatography and reversed-phase chromatography. Conclusion: AG-β-CD is capable of highly efficient purification of daidzein.

Purification technology of puerarin by agar gel microspheres / 中国中药杂志

Puerarin is the main active component of flavonoids in Puerariae Lobatae Radix. In this study, agar gel microspheres bonded with β-cyclodextrin (AG-β-CD) were synthesized by using economical agar, and then high-purity puerarin was obtained with AB-8 through high-yield separation. With purity and yield of puerarin, and chromatographic purity of related impurities as indexes, four macroporous resins of different properties, namely ADS-7 (high polarity), ADS-17 (medium polarity), ADS-21 (polarity) and AB-8 (weak polarity), were selected for separation of puerarin and technological optimization. In addition, the AG-β-CD purification process was optimized and verified. The results showed that, AB-8 resins showed the best effect and selected as the pre-treatment resins for crude puerarin, and puerarin with the purity of 87.68% showed a recovery rate of 89.66%. The optimized purification process parameters of AG-β-CD included mobile phase (15% ethanol), loading capacity (the ratio of loading amount to column volume) (1.33 g•L⁻¹), sample concentration (8 g•L⁻¹) and flow rate (1 mL•min⁻¹), puerarin with the purity of 95% showed a recovery rate of more than 97%.

A rapid detection method for single nucleotide polymorphisms based on ligase-agarose gel electrophoresis / 重庆医学

Objective To establish a simple,rapid and sensitive nucleotide polymorphisms genotyping method in order to conduct the routine clinical detections under the simple laboratory condition by this method.Methods Based on the ligase-agarose gel electrophoresis,the oligonucleotide detection probes of mutational sites was designed.The detection underwent the detection probe connecting,purification and universal amplification,finally the mutation genotypes of detection sites were judged by the ap-peared bands in the agarose gel electrophoresis(AGE).With the 3 SNP sites EGFR,c.2573T>G(L858R),EGFR,c.2582T> A (L861Q)and EGFR,c.2155 G>T(G719C)in epidermal growth factor receptor(EGFR)gene as the detection objects,the plasmid template and plasma circulating DNA sample in lung cancer were performed the detection.Results The established method was easy to operate with higher specificity and sensitivity.After 20-30 cycles of PCR amplification,the genotype of detection sites was clearly estimated according to the amplification band.When detecting the mixed alleles in the heterogeneous sample,minimal 2.5%mutation alleles could be detected out.This method and the direct sequencing method could respectively detect 6 cases and 2 cases of heterozygotes mutation in the SNP site of L858R among 62 samples of lung cancer.Conclusion The established detection method for SNP genotyping is suitable to the routine mutation detection on the heterogeneous samples under the simple laboratory condi-tion.

Evaluation of major methods of hemoglobin analysis / 中华检验医学杂志

Hemoglobinopathy is a kind of hereditary hematonosis caused by the disproportion among normal hemoglobins or formation of abnormal hemoglobins.Hemoglobin analysis plays an important role in screening and diagnosing hemoglobinopathy.Emerging methods have been applied continuously to hemoglobinometry since the early 20th century.Nowadays,agarose gel electrophoresis,high performance liquid chromatography and capillary electrophoresis are widely used with mass spectrometry as the latest applied method.All these methods have their own features.Appropriate combination of these methods will lead to more scientific and reliable results.

Enzootic bovine leucosis ­ a case report / Leucose enzoótica bovina ­ relato de caso

Enzootic bovine leucosis is an infectious disease of cattle caused by the bovine leukemia virus that results in lymphoma within target tissues. Cattle might demonstrate four clinicopathological age-related manifestations of the disease: juvenile, adult, thymic, and cutaneous form. This article describes the unusual manifestation of this disease in a 4-yr-old cow. Regional lymph nodes were enlarged during clinical examination. Peripheral and internal lymph nodes, as well as the vagina, uterus, spleen, liver, heart, thoracic vertebrae, eye and the thoracic and abdominal cavities demonstrated lymphoma at necropsy. Bovine enzootic leucosis was confirmed by histopathology and agar gel immunodifusion.

A leucose enzoótica bovina é uma doença infecciosa de bovinos causada pelo vírus da leucemia bovina que produz linfoma em tecidos alvos. Bovinos podem demonstrar quatro manifestações clínico-patológicas da doença relacionadas à idade: forma juvenil, adulta, tímica e cutânea. Esse artigo descreve a manifestação incomum dessa doença em uma vaca de quatro anos de idade. Os linfonodos regionais apresentaram-se aumentados no exame clínico. Linfoma foi observado nos linfonodos periféricos e internos bem como na vagina, útero, baço, fígado, coração, vértebras torácicas, olho e nas cavidades torácica e abdominal durante a necropsia. A leucose enzoótica bovina foi confirmada na histopatologia e pela imunodifusão em gel de ágar.

Detection of HIV-1 p24 based on gold nanoparticle probe and PCR / 中华检验医学杂志

ObjectiveTo establish a novel assay for HIV-1 p24 ultrasensitive detection based on Gold Nanoparticle Probe (GNP) and PCR.MethodsSandwich ELISA method was established by a pair of anti-p24 monoclonal antibodies (mAbs),1G12 and 1D4,and was used to detect recombinant HIV-1 p24 antigen.The bio-barcode DNA was 47 bp,selected from genome of Arabidopsis,and formed double-stranded DNA by hybridization with the capture DNA (complementary with bio-barcode DNA) modified with sulfhydryl.Then double-stranded DNA were conjugated on the surface of 1D4-modified gold nanoparticles by sulfhydryl,and the Gold Nanoparticle Probe was produced.1G12 was precoated in the micropaltes,and in the presence of target recombinant HIV-1 p24 protein,a sandwich immuno-complex would form by adding GNP.Then the bio-barcode DNA in the immuno-complex were released by heating as detection signal,and consequently characterized by the polymerase chain reaction (PCR) with synthesized special primers and analyzed by 4％ agar gel electrophoresis,so HIV-1 p24 antigen could be evaluated.The sensitivity comparison between the new assay and ELISA can be done.ResultsSandwich ELISA was used to quantify HIV-1 p24 antigen by monoclonal antibodies 1G12 and 1D4,and the limit of detection (LOD) was 1000 pg/ml.The new GNP assay was established by the same pair of antibodies,combined with PCR and agar gel electrophoresis,and was used to indirectly detect HIV-1 p24 antigen.The band intensity of PCR products paralleled with the quantity of HIV-1 p24 antigen,and the limit of detection (LOD) could reach down to 1 pg/ml.ConclusionThe new assay based on GNP and PCR was efficient in the detection of HIV-1 p24,which is at least 3 orders of magnitude more sensitive than traditional ELISA.

Anticorpos anti-Brucella canis e anti-Brucella abortus emcães de Araguaína, Tocantins / Antibodies anti-Brucella canis and anti-Brucella abortus in dogs from Araguaína, Tocantins,Brazil

Os objetivos deste estudo foram determinar a soroprevalência da infecção por Brucella canis e Brucella abortus e avaliaros possíveis fatores de risco associados à infecção em cães no município de Araguaína, Tocantins. Soros de 374 cães,pertencentes à zona urbana do município de Araguaína-Tocantins, foram analisados pelas técnicas de imunodifusãoem ágar gel (IDGA), para pesquisa de anticorpos contra Brucella canis, e antígeno acidificado tamponado (AAT)e polarização fluorescente (FPA) para detecção de anticorpos contra Brucella abortus. Dos 374 soros testados parapresença de anticorpos contra B. abortus, 21 foram reagentes no AAT, entretanto todos foram negativos pela FPA. Àprova do IDGA 167 animais foram reagentes resultando em uma prevalência para B. canis de 44,53% (IC 95%; 39,43 a49,72). A avaliação de possíveis fatores de risco associados à soropositividade para B. canis não revelou a existência derelação entre a infecção e as variáveis individuais estudadas. Assim, o presente estudo permite concluir que não houveanimais infectados por B. abortus e que a infecção por B. canis está disseminada nos cães do município de Araguaína,Tocantins.

The aims of the present study were to determine the seroprevalence of infection by Brucella canis and Brucella abortusand to evaluate possible risk factors for infection in dogs from Araguaína, Tocantins, Brazil. Sera from 374 dogs, of theurban zones of the municipality, from both sexes, were submitted to the agar-gel immunodiffusion for Brucella canisantibodiesand to rose Bengal test (AAT) and fluorescence polarization assay (FPA) for Brucella abortus-antibodies.From the 374 tested dogs, 21 reacted in the AAT, but no one was positive in the FPA. The seroprevalence of B. canisinfection found in Araguaína, Tocantins, Brazil, was 44.53% (95% IC; 39.43 to 49.72). No association was found amongseropositivity for B. canis and the risk factors studied. Thus, data from the present study showed that there was noinfection by B. abortus among dogs in the sample and that infection by B. canis is widespread and at high prevalence inAraguaína, Tocantins, Brazil.

Prueba de sensibilidad antimicrobiana de cepasde Salmonella grupo D (móviles e inmóviles) aisladasde ponedoras comerciales en Colombia / Antimicrobial susceptibility test of isolates of Salmonella group D (mobile and non mobile) from commercial laying hens in Colombia

Las infecciones originadas por bacterias del género Salmonella son una de las principalescausas de pérdidas económicas en la industria avícola, se caracterizan generalmentepor la presentación de cuadros diarreicos y septicémicos que llevan a las aves a unamarcada disminución en la producción y a la muerte. En Colombia, debido al efectonegativo que produce Salmonella spp. en las aves, y con el objetivo de poder controlarla enfermedad, se utiliza una gran variedad de productos antimicrobianos, de los cuales no se posee suficiente información acerca de su comportamiento en cuanto asensibilidad y resistencia frente a las cepas de Salmonella spp. de campo. El objetivo de este estudio fue determinar la respuesta de 20 cepas de Salmonellas grupo D (móviles einmóviles) aisladas de aves ponedoras comerciales en Colombia frente a diferentes antimicrobianos. Para su aislamiento y tipificación se utilizaron técnicas microbiológicas convencionales, pruebas bioquímicas, serológicas y pruebas de susceptibilidad a los antibióticos por difusión en agar. Los resultados revelaron una resistencia total hacia la estreptomicina, seguida de altas resistencias para tetraciclina y florfenicol, y una menor resistencia a productos como fosfomicina y cloramfenicol.

Infections caused by Salmonella bacteria are a major cause of economic losses in thepoultry industry, because caused mainly by the presentation of diarrheas and septicemic birds leading to a marked decrease in the production death. In Colombia due to the negative effect by Salmonella spp. in poultry, and with the aim of controlling the disease, the people have been using a variety of antimicrobials, which do not possess sufficient information about its behavior in terms of sensitivity and resistance againststrains of Salmonella spp. field. The aim of this study was to determine the response of20 strains of Salmonella group D (mobile and non mobile) isolated from commercial laying hens in Colombia against different antimicrobials. For the isolation and characterization are using conventional microbiological techniques, biochemical tests, serological testing and antibiotic susceptibility by agar diffusion. The results revealed a total resistance to streptomycin, followed by tetracycline and Florfenicol and less resistance to products such as Fosfomycin and chloramphenicol.

Study on the Yersinia pestis plasmid along the Qinghai-Tibet Railway / 中国地方病学杂志

Objective To detect the Yersinia pestis plasmid and molecular weight along the Qinghai-Tibet Railway.Methods Yersinia pestis plasmids molecular weight detected and analyzed using alkaline lysis,phenol-chloroform extraction of Yersinia pestis plasmid by agarose gel electrophoresis.Results The 18 Yersinia pestis strains of Qinghai-Tibet Railway contained 6×106,45×106,52×106,65×106,92×106plasmid,varing in the range of the 52×106-92×106.Conclusions The Yersinia pestis of Qinghai-Tibet Railway has a standardplasmid graphics,with the biggest Yersinia pestis plasmid changing in a certain regular degree,which providessignificance in the study of plague natural foci of the spatial structure and the genetic.characteristics of Yersiniapestis.

Electrophoresis of serum proteins in parturient women / 中华检验医学杂志

0.05). Conclusion The changes of serum protein electrophoresis results in the parturient women were mainly presented with the decreased in albumin and ? globin levels, increased percent of ? 1,? 2 and ? globins, increased percent of ? 2 and ? globins markedly related with increased ? and ? lipoprotein. Agarose gel electrophoresis as a screening method for component of serum proteins is valuable.

Clinical application of protein electrophoresis using non-concentrated urine samples / 中华检验医学杂志

Objectives To analyze the various protein components in urine and to define the types of proteinuria. Methods Sodium dodecyl sulfate argarose gel electrophoresis was used to analyze 86 non concentrated urine samples from patients with various renal injury. Results According to the images of urine protein electrophoresis, proteinuria can be classified into five types: glomerular, tubular, mixed, over flow, and physiological. Results from 16 cases of renal biopsy showed glomerular type, in 12 cases mixed type in 3, physiological type in 1. Conclusion This method is highly sensitive, simple, less time consuming and easy for long term preservation of results.