Abstract Leptospirosis is a worldwide zoonose and is endemic in many countries. This disease is maintained in nature by chronic renal infection of carrier animals, being rodents and other small mammals the most important reservoirs. Also, significant sources of human infection are domestic animals, such as livestock and dogs. The wild boar (Sus scrofa) is an introduced species from Europe which is widespread in America and particularly in the Center and South of Argentina. This species is highly valued by hunters in the region and their meat is consumed more often. In many countries of the world (Europe, USA and Australia) studies of seroprevalence have been carried out, the seroreactivity does not mean that the wild boar has clinical symptoms of leptospirosis or that wild boars are maintenance host of this pathogen. However, these animals have been in contact to leptospiras in their environment in the past. This study has the objective to molecularly genotype the pathogenic Leptospira sp. isolated strain obtained from fetuses of wild boars from Patagonia Argentina. Four fetuses were aborted from a wild boar (Sus scrofa) in Patagonia, the southern region of Argentina. Necropsy was performed of the 4 fetuses and samples of kidneys, liver, spleen and lung were cultivated in Fletcher and EMJH mediums. Also, samples of liver, spleen, lung and kidney of fetuses were processed and analyzed by direct immunofluorescence. Multiple Locus Variable number tandem repeats Analysis (MLVA) was used to characterize the isolated strain. The genetic profile of the isolated pathogenic Leptospira sp. strain was identical to the profile of Leptospira borgpetersenii serovar Castellonis Castellon 3, serogroup Ballum. To the best of our knowledge this is the first isolation of Leptospira spp. from a wild boar fetus.

Resumen La leptospirosis es una zoonosis mundial y es endémica en muchos países. Esta enfermedad se mantiene en la naturaleza por la infección renal crónica de los animales portadores; los roedores y otros mamíferos pequeños son los reservorios más importantes. Además, otras fuentes importantes de infección para el humano son los animales domésticos, como el ganado y los perros. El jabalí (Sus scrofa) es una especie introducida de Europa que está muy extendida en América y particularmente en el centro y sur de Argentina. Esta especie es muy valorada por los cazadores de la región y su carne se consume con mayor frecuencia. En muchos países del mundo (Europa, EE. UU. y Australia) se han realizado estudios sobre seroprevalencia, la seroreactividad no significa que el jabalí manifieste síntomas clínicos de leptospirosis o que los jabalíes sean reservorios de este patógeno bacteriano. Sin embargo, estos animales han estado en contacto con leptospiras en su entorno en el pasado. Este estudio tiene el objetivo de tipificar molecularmente la cepa aislada obtenida a partir de 4 fetos de jabalíes (Sus scrofa) provenientes de la Patagonia argentina. Se realizaron necropsias de los 4 fetos y se cultivaron muestras de riñones, hígado, bazo y pulmón en medios Fletcher y EMJH. Además, las muestras de hígado, bazo, pulmón y riñón de los fetos se procesaron y analizaron por inmunofluorescencia directa. Se utilizó el análisis de repeticiones en tándem de número variable de locus múltiple (MLVA) para caracterizar la cepa aislada. El perfil genético de la cepa de leptospira fue idéntica al perfil de Leptospira borgpetersenii serovar Castellonis Castellon 3 perteneciente al serogrupo Ballum. Hasta donde sabemos, este es el primer aislamiento de Leptospira spp. de un feto de jabalí.

Abstract We here describe the first isolation and molecular typing of Leptospira borgpe-tersenii serovar Hardjo Bovis in Argentina, obtained from urine of aborted cows from abreeding herd located in Saladillo, Buenos Aires Province. The abortions occurred in coincidence with important floods with many cows presenting suspicious serological titers and subsequentseroconversion. The percentage of abortions was 3.5% of a herd of 1700 cows and the microor-ganism was isolated from 7 of the 20 urine samples obtained.

Resumen Se describe el primer aislamiento y la tipificación molecular de Leptospira borgpetersenii serovar Hardjo Bovis en Argentina, obtenido a partir de orina de vacas abortadas de unrodeo de cría ubicado en Saladillo, provincia de Buenos Aires. Los abortos coincidieron con unperíodo de importantes inundaciones, en el que varios animales presentaron títulos serológicossospechosos y posterior seroconversión. El porcentaje de abortos alcanzó el 3,5% del total delrodeo, compuesto por 1700 vacas, y se aisló el microorganismo en 7 de 20 muestras de orinaobtenidas.

Leptospirosis is a zoonosis having worldwide distribution. The objective of this work was to develop a molecular technique to differentiate pathogenic Leptospira spp. A region of adhesin ligB, present only in the pathogenic species was amplified by PCR and sequenced. ligBRpet and ligBFpet primers were used, which amplified the target DNA from pathogenic L. interrogans reference strains serovars Pomona strain Pomona, Canicola strain Hond Utrecht IV, Copenhageni strain M 20, Wolffi strain 3705, Pyrogenes strain Salinem, Hardjo strain Hardjoprajitmo, L. borgpetersenii serovar Castellonis strain Castellon 3 and 4 pathogenic strains isolated from bovines, pigs, rats and opossums. L. biflexa serovars Patoc strain Patoc i and Andamana strain Andamana were not amplified. Sequencing of the amplified products exhibited sufficient variation among serovars, which differentiates them.

La leptospirosis es la zoonosis de mayor distribución mundial. El objetivo del preReacción en cadena sente trabajo fue desarrollar una técnica molecular que diferencie leptospiras patógenas. Se amplificó mediante PCR y se secuenció una región de la adhesina ligB, presente solo en las especies patógenas. Se utilizaron los iniciadores ligBFpet y ligBRpet. Dichos iniciadores lograron amplificar el ADN blanco de 6 cepas patógenas referenciales de Leptospira interrogans (serovar Pomona cepa Pomona, serovar Canicola cepa Hond Utrecht IV, serovar Copenhageni cepa M 20, serovar Wolffi cepa 3705, serovar Pyrogenes cepa Salinem y serovar Hardjo cepa Hardjoprajitmo) y el de Leptospira borgpetersenii serovar Castellonis cepa Castellon 3; también el de 4 cepas patógenas aisladas de bovino, porcino, rata y comadreja. En las 2 cepas referenciales no patógenas utilizadas, Leptospira biflexa serovar Patoc cepa Patoc i y L. biflexa serovar Andamana cepa Andamana, no hubo amplificación. La secuenciación de los productos amplificados expuso una suficiente variación entre los serovares estudiados, que permite diferenciarlos.

O objetivo do presente estudo foi descrever um caso de isolamento de espécie patogênica de Leptospira interrogans em amostra de urina de um humano morador da zona rural do Município de Cruz Alta, Estado do Rio Grande do Sul. De cada amostra de urina, uma alíquota foi semeada nos meios Fletcher e Ellinghausen - McCullough - Johnson - Harris (EMJH). As amostras, nas quais houve crescimento de espiroquetas, foram encaminhadas para o Laboratório de Leptospirose do Instituto de Patobiologia do Instituto Nacional de Tecnologia Agropecuária, Buenos Aires, Argentina e foram tipificadas pela técnica Multiple Locus of Variable Number Tandem Repeat (MLVA). De um residente do sexo masculino da área rural do município de Cruz Alta, foi isolada Leptospira interrogans sorovariedade Copenhageni cepa Fiocruz L1-130, uma descoberta muito importante e que serve como um alerta por caracterizar uma situação de risco de epidemia de leptospirose por uma cepa patogênica. Os profissionais de saúde precisam ser mais comprometidos com a atenção primária à saúde no Brasil e rotineiramente aplicar ações de medicina preventiva nas comunidades rurais, a fim de obter sucesso no controle da leptospirose e de outras importantes zoonoses

The aim of this study was to describe the isolation of a pathogenic strain of Leptospira interrogans from the urine sample of a male human living in the rural area of the County of Cruz Alta, Rio Grande do Sul. An aliquot of each urine sample was sown in a Fletcher and Ellinghausen - McCullough - Johnson - Harris (EMJH) media. Samples in which there was growth of spirochetes were sent to the Leptospirosis Laboratory of the Institute of Pathobiology in the National Institute of Agricultural Technology, Buenos Aires, Argentina and were typified by the Multiple Locus of Variable Number Tandem Repeat technique (MLVA). Leptospira interrogans serovar Copenhageni strain Fiocruz L1-130 was isolated, and this is a very important finding that serves as a warning to characterize risk situation of leptospirosis epidemic by a pathogenic strain. Health professionals need to be more committed to the primary health care in Brazil and routinely apply actions of preventive medicine in rural communities in order to get success in the control of leptospirosis and other important zoonoses

Leptospirosis is an infectious disease of wide global distribution, which is endemic in Argentina. The objective of this study was to obtain the genetic profiles of Leptospira spp. strains isolated from clinical cases of dogs in the province of Buenos Aires by the multiple-locus variable-number tandem repeat analysis (MLVA). Eight isolated canine strains were genotyped by MLVA, obtaining the identical profile of Leptospira interrogans serovar Canicola Hond Utrecht IV in the strains named Dogy and Mayo. The strains named Bel, Sarmiento, La Plata 4581 and La Plata 5478 were identical to the profile of the genotype of L. interrogans serovar Portlandvere MY 1039.The strain named Avellaneda was identical to the genotype profile of L. interrogans serovar Icterohaemorrhagiae RGA and the strain named SB had the same profile as the L. interrogans serovar Pomona Baires genotype and was similar to the profile of serovar Pomona Pomona genotype. It would be useful to include a larger number of isolates from different dog populations in various provinces of Argentina and to characterize the genetic profiles of the strains circulating in the country. The information obtained will be useful for the control of leptospirosis in the dog population.

Leptospirosis is the most widespread zoonosis in the world and significant efforts have been made to determine and classify pathogenic Leptospira strains. This zoonosis is maintained in nature through chronic renal infections of carrier animals, with rodents and other small mammals serving as the most important reservoirs. Additionally, domestic animals, such as livestock and dogs, are significant sources of human infection. In this study, a multiple-locus variable-number tandem repeat analysis (MLVA) was applied to genotype 22 pathogenic Leptospira strains isolated from urban and periurban rodent populations from different regions of Argentina. Three MLVA profiles were identified in strains belonging to the species Leptospira interrogans (serovars Icterohaemorrhagiae and Canicola); one profile was observed in serovar Icterohaemorrhagiae and two MLVA profiles were observed in isolates of serovars Canicola and Portlandvere. All strains belonging to Leptospira borgpetersenii serovar Castellonis exhibited the same MLVA profile. Four different genotypes were isolated from urban populations of rodents, including both mice and rats and two different genotypes were isolated from periurban populations.

Introduction: the Leptospira genus species are causative agents of leptospirosis, a disease that is considered the most widely spread zoonotic disease worldwide. In Argentina, leptospirosis is endemic and Santa Fe province has the highest number of human cases. Since mid-1980's, the pathogenic leptospira species isolated from animals and humans have been differenciated through DNA-DNA hybridization tests, resulting in new species: L. interrogans, L. kirschneri, L. weilii, L. noguchii, L. borgpetersenii, L. santarosai, L. meyeri, L. inadai, L. faineri y L. alexanderi. Objectives: to isolate and to characterize by molecular test leptospiras from water poured into a channel that runs through Casilda City in Santa Fe Province, Argentina. Methods: six samples of water from the channel were cultured after having been filtered through 0.22 µm, Millpore filtres in EMJH and Fletcher media to isolate leptospires. They were incubated at 30 °C for 15 days, and weekly observed through dark field microscopy. Polymerase chain reaction assay was used under specific conditions (Sugathan, 2005), with two sets of primers (Gravekamp, 1993), to determine whether the isolates were pathogenic. The molecular technique for genotyping was Multiple-Locus Variable-number tandem repeats Analysis (MLVA). Results: five Leptospira spp. isolates were obtained of which 2 were positive to PCR, all of which determined that they were pathogenic leptospiras. MLVA genotyping allowed the observation of a pattern similar to that of L. borgpetersenii species in one pathogenic isolates, but the other isolate was not identified. Conclusions: in the City where the study was carried out, with a population of about 40,000 inhabitants, a L. borgpetersenii species was identified for the first time in urban water sources, with the potential risk that it may pose for human and animal populations.

Introducción: las especies del género Leptospira son los agentes causales de la leptospirosis, enfermedad considerada como la zoonosis de mayor distribución en el mundo.En Argentina reviste carácter endémico. La provincia de Santa Fe registra el mayor número de casos humanos. Desde mediados de la década de 1980, las especies patógenas de leptospiras aisladas de animales y humanos fueron diferenciadas sobre la base de estudios de hibridización ADN-ADN, surgiendo nuevas especies: L. interrogans, L. kirschneri, L. weilii, L. noguchii, L. borgpetersenii, L. santarosai, L. meyeri, L. inadai, L. faineri y L. alexanderi. Objetivo: aislar y caracterizar mediante métodos moleculares, leptospiras de fuentes de agua que vierten en un canal que atraviesa la ciudad de Casilda, Santa Fe, en Argentina. Métodos: se sembraron 6 muestras de agua de las vertientes al canal, previa filtración con filtros Millipore de 0,22 µm, en medios EMJH y Fletcher para aislamiento de leptospiras. Se incubaron en estufa a 30 °C durante 15 días, se observaron semanalmente mediante microscopia de campo oscuro. Se implementó la técnica de reacción en cadena de la polimerasa bajo las condiciones específicas (Sugathan, 2005), con dos juegos de cebadores (Gravekamp, 1993), que permiten detectar la presencia de ADN de leptospiras patógenas. La técnica molecular utilizada para genotipificar fue multiple-locus variable-number tandem repeats analysis (MLVA). Resultados: se obtuvieron 5 aislamientos de Leptospira spp., de los cuales 2 resultaron positivos a la reacción en cadena de la polimerasa, determinando que se trataba de leptospiras patógenas. Mediante la genotipificación por MLVA se pudo observar que uno de los aislamientos patógenos mostró un patrón correspondiente a la especie Leptospira borgpetersenii, no siendo identificable la otra cepa. Conclusiones: en la ciudad del estudio, que tiene alrededor de 40 000 habitantes, se logró identificar por primera vez una cepa de Leptospira borgpetersenii de fuentes de aguas urbanas, con el peligro potencial que esto representa para la población humana y animal.