ABSTRACT
Abstract Occurrence of Ureaplasma diversum (U. diversum) has been associated with repro-ductive failures in cattle and detected in pigs with and without pneumonia. However, its rolein the porcine respiratory disease complex (PRDC) is unclear. A cross-sectional study was con-ducted in abattoirs, inspecting 280 pig lungs from eight herds. All the lungs were inspected,processed and classified according to the histopathological analysis. Moreover, bronchoalveolarlavage (BAL) specimens were collected and processed by PCR for detection of U. diversum andMycoplasma hyopneumoniae (M. hyopneumoniae). Ureaplasma sp.---U. diversum and M. hyop-neumoniae were detected in 17.1% and 29.3% of the analyzed BAL specimens, respectively. Theconcomitant presence of both microorganisms was detected in 12.5% of the inspected lungs.Both agents were found in lungs with and without pneumonia. M. hyopneumoniae was detectedin 31.8% of pig lungs with enzootic pneumonia-like lesions, while Ureaplasma sp.---U. diversumwas detected in 27.5% of lungs with these lesions. This descriptive exploratory study providesinformation for future experimental and field-based studies to better define the pathogenicrole of this organism within the PRDC.
Resumen La presencia de Ureaplasma diversum se ha asociado a fallas reproductivas en el ganado bovino y se ha detectado en cerdos con y sin neumonía. Sin embargo, su participación en el complejo de enfermedades respiratorias porcinas (CERP) no es clara. Se llevó a cabo un estudio transversal en matadero, inspeccionando 280 pulmones de cerdo provenientes de ocho piaras. Todos los pulmones fueron inspeccionados, procesados y clasificados según el análisis histopatológico. También se colectaron muestras de lavado broncoalveolar (LBA) y se procesaron mediante PCR para la detección de U. diversum y Mycoplasma hyopneumoniae. Ureaplasma sp.-U. diversum y M. hyopneumoniae se detectaron en el 17,1% y en el 29,3% de los LBA analizados, respectivamente. La presencia concomitante de ambos microorganismos se detectó en el 12,5% de los pulmones inspeccionados. Ambos agentes se encontraron en pulmones con y sin neumonía. M. hyopneumoniae se detectó en el 31,8% de los pulmones con lesiones compatibles con neumonía enzoótica, mientras que Ureaplasma sp.-U. diversum se detectó en el 27,5% de los pulmones con estas lesiones. Este estudio exploratorio descriptivo proporciona información para futuros estudios experimentales y de campo tendentes a definir mejor el papel patógeno de este organismo dentro del CERP.
ABSTRACT
Abstract The aim of this short communication is to describe a case of subfertility and otheranomalies associated with the presence of Mycoplasma spumans and Mycoplasma maculosumin a Bernese Mountain Dog kennel. After the arrival of two dogs from abroad, some fertilitydisorders, such as unsuccessful mating, pregnancy losses and abnormal sperm analysis results,were observed. Two consecutive samplings (vaginal swabs) of three and two bitches with prob-lems, respectively, were performed and M. spumans and M. maculosum were identified by PCRand sequencing. After treatment for 15 days with doxycycline and 9 days with azithromycin,successful pregnancies were achieved and the results of the sperm analyses were reversed.Considering that no other infectious agents causing subfertility problems were detected andthat no management measures or other medication apart from these antibiotics were applied,it was concluded that fertility problems were due to the presence of these two Mycoplasmaspecies.
ABSTRACT
ABSTRACT: To assess the success of a segregated medicated early weaning protocol for elimination of Actinobacillus pleuropneumoniae, ten consecutive batches of 100 pigs per batch weaned at 7-9 days of age were monitored at 21-22 weeks of age looking for presence of productive cough, presence of antibodies against the agent and pleuropneumonia-compatible lung lesions at slaughter. Also, whole tonsils were processed for A. pleuropneumoniae identification by both bacteriological isolation and nested-PCR using a direct method. Positive serological test (1.4%) and PCR (3.5%) results, suggested that A. pleuropneumoniae could not be eradicated in all batches, even using segregated medicated early weaning protocol.
RESUMO: Para avaliar o sucesso de um protocolo de desmame precoce segregado medicado para a eliminação de Actinobacillus pleuropneumoniae, dez lotes consecutivos de 100 suínos por lote desmamados aos 7-9 dias de idade foram monitorados às 21-22 semanas de idade procurando a presença de tosse produtiva, presença de anticorpos contra o agente e lesões pulmonares compatíveis com pleuropneumonia no abate. Além disso, as tonsilas inteiras foram processadas para a identificação de A. pleuropneumoniae por isolamento bacteriológico e nested PCR usando um método direto. Os resultados serológicos (1,4%) e PCR (3,5%) positivos sugerem que não foi possível erradicar em todos os lotes, mesmo usando um protocolo de desmame precoce segregado medicado.
ABSTRACT
Algunas especies del género Brachyspira, como Brachyspira pilosicoli, Brachyspira intermedia y Brachyspira alvinipulli, son especies patógenas capaces de producir enfermedad en gallinas ponedoras. En nuestro país, la presencia de B. pilosicoli y otras especies de Brachyspira ha sido informada en cerdos y en perros, pero no existen antecedentes de su presencia en aves de corral. En este estudio se analizaron muestras de materia fecal y de contenido de ciego de 34 gallinas ponedoras de 4, 12 y 24 meses provenientes de 2 establecimientos por medio del aislamiento, la realización de pruebas bioquímicas y reacción en cadena de la polimerasa. B. pilosicoli y Brachyspira spp. fueron identificadas en muestras tomadas de aves de 12 y 24 meses de edad
Some species of the genus Brachyspira such as Brachyspira pilosicoli, Brachyspira intermedia and Brachyspira alvinipulli are pathogenic species capable of producing disease in laying hens. In our country, the presence of B. pilosicoli and other species of Brachyspira has been reported in pigs and dogs but there is no record of their presence in poultry. Fecal and cecal content samples from 34 laying hens of 4, 12 and 24 months of age from two farms were analyzed by isolation, biochemical tests and PCR. B. pilosicoli and Brachyspira spp. were identified in samples taken from laying hens of 12 and 24 months of age
Subject(s)
Animals , Poultry/microbiology , Brachyspira/isolation & purification , Brachyspira/classification , Bacterial Infections/veterinary , Polymerase Chain Reaction/methods , Feces/microbiologyABSTRACT
Diferentes especies del género Mycoplasma pueden afectar al ganado bovino y causar varias enfermedades. La técnica de PCR, secuenciación y posterior análisis de la región ITS 16S-23S ARNr ha mostrado que existe una importante variabilidad interespecies entre Mollicutes. Se realizó la amplificación (región ITS 16S-23S ARNr) de 16 aislamientos sospechosos de corresponder a alguna especie de Mycoplasma, que habían sido obtenidos de muestras de leche provenientes de rodeos lecheros. Catorce de esos aislamientos fueron PCR positivos. Para confirmar la identidad de Mycoplasma bovis, dichos aislamientos fueron evaluados por otra PCR especie-específica. Siete aislamientos dieron un resultado positivo. Los productos de la PCR de la ITS 16S-23S ARNr de un aislamiento identificado como M. bovis y de otros dos aislamientos identificados como no-M. bovis fueron seleccionados al azar, secuenciados y analizados. Las tres secuencias (A, B y C) mostraron 100 % de similitud con cepas de M. bovis, Mycoplasma canadense y Mycoplasma californicum, respectivamente
Different species of Mycoplasma can affect bovine cattle, causing several diseases. PCR sequencing and further analysis of the 16S-23S rRNA ITS region have shown a significant interspecies variability among Mollicutes. Sixteen suspected isolates of Mycoplasma spp. obtained from milk samples from dairy herds were amplified (16S-23S rRNA ITS region). Fourteen out of those 16 suspected Mycoplasma spp. isolates were PCR-positive. To confirm the identity of Mycoplasma bovis, these 14 isolates were tested by another species-specific PCR. Seven of the isolates rendered a positive result. The products of 16S-23S rRNA ITS PCR from one isolate that was identified as M. bovis and from two other isolates, identified as non- M. bovis were randomly selected, sequenced and analyzed. The three sequences (A, B and C) showed 100% similarity with M. bovis, Mycoplasma canadense and Mycoplasma californicum respectively
Subject(s)
Animals , Cattle , Argentina/epidemiology , Cattle Diseases/diagnosis , Mycoplasma Infections/diagnosis , RNA, Ribosomal, 16S/analysis , RNA, Ribosomal, 23S/analysis , Bacterial Typing Techniques/methods , Tenericutes/isolation & purification , Mycoplasma bovis/isolation & purificationABSTRACT
O objetivo deste estudo foi monitorar a presença de M. hyopneumoniae em granjas suínas durante a implementação de programas de erradicação utilizando diferentes técnicas de diagnóstico focalizando no PCR. Trabalhou-se com uma empresa que possuía três granjas, uma parto-terminação (390 matrizes), uma múltiplo-sítio (4100 matrizes) e uma nova granja que povoava suas novas instalações. Nas duas primeiras, foi desenvolvido um programa de despovoamento parcial para erradicar a pneumonia enzoótica suína, a última foi povoada pelos suínos dos anteriores após a erradicação. Nos três rebanhos, os suínos foram monitorados por: sorologia (ELISA), PCR, lesões pulmonares macro e microscópicas e a presença de tosse não produtiva. A ausência de tosse, a baixa porcentagem de suínos soropositivos na fase de terminação e a baixa proporção de lesões pulmonares no abate sugerem que a pneumonia enzoótica suína foi erradicada, mas não o agente causativo -M. hyopneumoniae- cujo DNA foi detectado pela PCR, mostrando diferentes comportamentos de acordo com o rebanho.
The aim of this study was to monitor the presence of M. hyopneumoniae in pig farms during the implementation of eradication programs using different diagnostic techniques focusing on PCR. They worked with a company owner of three farms, a farrow-to-finish (390 sows), a multiple-site (4100 sows) and a new one that was populated its new facility. In the first two were developed a partial depopulation program to eradicate swine enzootic pneumonia, the latter one was populated with pigs after the previous eradication. In the three farms, the pigs were monitored by: serology (ELISA), PCR, macroscopic and microscopic lung lesions and the presence of non-productive cough. The absence of cough, low percentage of seropositive pigs in the finishing stage and the low proportion of lung lesions at slaughter suggest that swine enzootic pneumonia was eradicated, but not the causative agent -M. hyopneumoniae- whose DNA was detected by PCR showing different behaviors according to the herd.