G. Rodríguez, Ricardo Piñeros, Germán Alonso Prada, C. Diaz, C. Venegas, C. Salazar, Carlos Trujillo, Laura Camila Nossa
{"title":"哥伦比亚昆迪纳马卡省克里奥尔马精液和阴道前液中钩端螺旋体的分子测定和血清学研究","authors":"G. Rodríguez, Ricardo Piñeros, Germán Alonso Prada, C. Diaz, C. Venegas, C. Salazar, Carlos Trujillo, Laura Camila Nossa","doi":"10.19052/MV.4258","DOIUrl":null,"url":null,"abstract":"The objective of this study was to serologically (microagglutination test) and molecularly— Leptospira spp. DNA by conventional polymerase chain reaction (PCR)—detect the exposition or presence of Leptospira spp. from blood, pre-ejaculatory fluid, and semen samples in Colombian Creole horses representative of this breed, in 44 breeding centers in the department of Cundinamarca. In Colombia, there are no studies related to the presence of leptospires in equine semen, and according to health plans designed for this species they are not vaccinated against this disease. Samples were collected from a total of 107 animals, selected by convenience sampling; after serum analysis, 35 were seroreactive (32.7%), corresponding to the Leptospira interrogans serogroup, serovars canicola, pomona, and grippotyphosa. Leptospira spp. DNA was detected by conventional PCR in two semen samples that represented 1.9% of the total samples. Using the dark-field technique, different bacterial forms were found in most of the pre-ejaculatory fluid samples, some of them compatible with Leptospira . Desquamated cells, crystals, and urates were also found. In addition, the bacterium was not isolated in the EMJH medium and no DNA was detected by the conventional PCR technique from the preejaculatory fluid.","PeriodicalId":21407,"journal":{"name":"Revue De Medecine Veterinaire","volume":"26 1","pages":"93-100"},"PeriodicalIF":0.0000,"publicationDate":"2017-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Determinación molecular de Leptospira spp. en semen y líquido preseminal y estudio serológico de caballos criollos en el departamento de Cundinamarca (Colombia)\",\"authors\":\"G. Rodríguez, Ricardo Piñeros, Germán Alonso Prada, C. Diaz, C. Venegas, C. Salazar, Carlos Trujillo, Laura Camila Nossa\",\"doi\":\"10.19052/MV.4258\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The objective of this study was to serologically (microagglutination test) and molecularly— Leptospira spp. DNA by conventional polymerase chain reaction (PCR)—detect the exposition or presence of Leptospira spp. from blood, pre-ejaculatory fluid, and semen samples in Colombian Creole horses representative of this breed, in 44 breeding centers in the department of Cundinamarca. In Colombia, there are no studies related to the presence of leptospires in equine semen, and according to health plans designed for this species they are not vaccinated against this disease. Samples were collected from a total of 107 animals, selected by convenience sampling; after serum analysis, 35 were seroreactive (32.7%), corresponding to the Leptospira interrogans serogroup, serovars canicola, pomona, and grippotyphosa. Leptospira spp. DNA was detected by conventional PCR in two semen samples that represented 1.9% of the total samples. Using the dark-field technique, different bacterial forms were found in most of the pre-ejaculatory fluid samples, some of them compatible with Leptospira . Desquamated cells, crystals, and urates were also found. In addition, the bacterium was not isolated in the EMJH medium and no DNA was detected by the conventional PCR technique from the preejaculatory fluid.\",\"PeriodicalId\":21407,\"journal\":{\"name\":\"Revue De Medecine Veterinaire\",\"volume\":\"26 1\",\"pages\":\"93-100\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-07-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revue De Medecine Veterinaire\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.19052/MV.4258\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Veterinary\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revue De Medecine Veterinaire","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19052/MV.4258","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Veterinary","Score":null,"Total":0}
Determinación molecular de Leptospira spp. en semen y líquido preseminal y estudio serológico de caballos criollos en el departamento de Cundinamarca (Colombia)
The objective of this study was to serologically (microagglutination test) and molecularly— Leptospira spp. DNA by conventional polymerase chain reaction (PCR)—detect the exposition or presence of Leptospira spp. from blood, pre-ejaculatory fluid, and semen samples in Colombian Creole horses representative of this breed, in 44 breeding centers in the department of Cundinamarca. In Colombia, there are no studies related to the presence of leptospires in equine semen, and according to health plans designed for this species they are not vaccinated against this disease. Samples were collected from a total of 107 animals, selected by convenience sampling; after serum analysis, 35 were seroreactive (32.7%), corresponding to the Leptospira interrogans serogroup, serovars canicola, pomona, and grippotyphosa. Leptospira spp. DNA was detected by conventional PCR in two semen samples that represented 1.9% of the total samples. Using the dark-field technique, different bacterial forms were found in most of the pre-ejaculatory fluid samples, some of them compatible with Leptospira . Desquamated cells, crystals, and urates were also found. In addition, the bacterium was not isolated in the EMJH medium and no DNA was detected by the conventional PCR technique from the preejaculatory fluid.
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