Genetic diversity and differentiation of 12 eastern Adriatic and western Dinaric native sheep breeds using microsatellites.

Nuclear genetic diversity and differentiation of 341 sheep belonging to 12 sheep breeds from Croatia and Bosnia and Herzegovina were examined. The aim of the study was to provide the understanding of the genetic structure and variability of the analysed pramenka sheep populations, and to give indications for conservation strategies based on the population diversity and structure information. The genetic variation of the sheep populations, examined at the nuclear level using 27 microsatellite loci, revealed considerable levels of genetic diversity, similar to the diversity found in other European indigenous low-production sheep breeds. Population-specific alleles were detected at most loci and in breeds analysed. The observed heterozygosity ranged from 0.643 (in Lika pramenka) to 0.743 (in Vlasic pramenka), and the expected heterozygosity ranged from 0.646 (in Lika pramenka) to 0.756 (in Dalmatian pramenka). Significant inbreeding coefficients were found for half of the populations studied and ranged from 0.040 (Pag island sheep) to 0.091 (Kupres pramenka). Moderate genetic differentiation was found between the studied sheep populations. The total genetic variability observed between different populations was 5.29%, whereas 94.71% of the variation was found within populations. Cres island sheep, Lika pramenka and Istrian sheep were identified as the most distinct populations, which was confirmed by the factorial analysis of correspondence and supported through a bootstrapping adjustment to correct for the difference in the sample sizes. The population structure analysis distinguished 12 clusters for the 12 sheep breeds analysed. However, the cluster differentiation was low for Dalmatian, Vlasic, Stolac and Krk pramenka. This systematic study identified Lika pramenka and Rab island sheep as those with the lowest diversity, whereas Istrian sheep and Pag island sheep had the highest. Conservation actions are proposed for Istrian, Rab and Cres island sheep, Lika and Kupres pramenka because of high estimated coefficients of inbreeding.

Analysis of genetic diversity in Bolivian llama populations using microsatellites.

South American camelids (SACs) have a major role in the maintenance and potential future of rural Andean human populations. More than 60% of the 3.7 million llamas living worldwide are found in Bolivia. Due to the lack of studies focusing on genetic diversity in Bolivian llamas, this analysis investigates both the genetic diversity and structure of 12 regional groups of llamas that span the greater part of the range of distribution for this species in Bolivia. The analysis of 42 microsatellite markers in the considered regional groups showed that, in general, there were high levels of polymorphism (a total of 506 detected alleles; average PIC across per marker: 0.66), which are comparable with those reported for other populations of domestic SACs. The estimated diversity parameters indicated that there was high intrapopulational genetic variation (average number of alleles and average expected heterozygosity per marker: 12.04 and 0.68, respectively) and weak genetic differentiation among populations (FST range: 0.003-0.052). In agreement with these estimates, Bolivian llamas showed a weak genetic structure and an intense gene flow between all the studied regional groups, which is due to the exchange of reproductive males between the different flocks. Interestingly, the groups for which the largest pairwise FST estimates were observed, Sud Lípez and Nor Lípez, showed a certain level of genetic differentiation that is probably due to the pattern of geographic isolation and limited communication infrastructures of these southern localities. Overall, the population parameters reported here may serve as a reference when establishing conservation policies that address Bolivian llama populations.

Analysis of mitochondrial DNA in Bolivian llama, alpaca and vicuna populations: a contribution to the phylogeny of the South American camelids.

The objectives of this work were to assess the mtDNA diversity of Bolivian South American camelid (SAC) populations and to shed light on the evolutionary relationships between the Bolivian camelids and other populations of SACs. We have analysed two different mtDNA regions: the complete coding region of the MT-CYB gene and 513 bp of the D-loop region. The populations sampled included Bolivian llamas, alpacas and vicunas, and Chilean guanacos. High levels of genetic diversity were observed in the studied populations. In general, MT-CYB was more variable than D-loop. On a species level, the vicunas showed the lowest genetic variability, followed by the guanacos, alpacas and llamas. Phylogenetic analyses performed by including additional available mtDNA sequences from the studied species confirmed the existence of the two monophyletic clades previously described by other authors for guanacos (G) and vicunas (V). Significant levels of mtDNA hybridization were found in the domestic species. Our sequence analyses revealed significant sequence divergence within clade G, and some of the Bolivian llamas grouped with the majority of the southern guanacos. This finding supports the existence of more than the one llama domestication centre in South America previously suggested on the basis of archaeozoological evidence. Additionally, analysis of D-loop sequences revealed two new matrilineal lineages that are distinct from the previously reported G and V clades. The results presented here represent the first report on the population structure and genetic variability of Bolivian camelids and may help to elucidate the complex and dynamic domestication process of SAC populations.

Utilización de un modelo animal para entrenamiento, en oxigenación por membrana extracorporea (ECMO) / The use of an animal model for extracorporeal membrane oxygenation (ECMO) training

ECMO es un procedimiento de rescate de recién nacidos (RN) con fallo respiratorio hipoxémico severo que no responde al tratamiento convencional. Previo a la instrumentación de esta técnica en pacientes, se realizó el entrenamiento experimental en animales. Existe escasa bibliografía sobre la utilización de porcinos como modelo animal en ECMO. Se reportan, en cambio, la implementación de otros animales, tales como el cordero. Objetivo: determinar la utilidad y el comportamiento modelo animal eligido, su respuesta al procedimiento de ECMO, describir la técnica utilizada y sus resultados. Método: se utilizaron dos porcinos de la raza Landrace, de 30 y 45 días de vida. Se canularon la vena yugular interna y la arteria carótida interna derechas; se realizó el ensamblado y purgado del circuito. El bypass se inició con un flujo de bomba de 20 mL/K/min, aumentandose hasta 100-120 mL/K/min; logrado un flujo de 80 mL/K/min se disminuyeron los parámetros de Asistencia Respiratoria Mecánica (ARM) a nivel de reposo. Durante el curso de ECMO se practicaron diferentes acciones relacionadas con el manejo del sistema de perfusión y evaluación del comportamiento clínico del modelo. Finalmente se suspendió electivamente el procedimiento; luego el animal fue dacanulado y recuperado. Resultados: tiempo promedio de ECMO: 24.5 horas. Signos vitales del animal estables. No hubo complicaciones relacionadas con el circito, ni presencia de sangrado sistémico. Se lograron tasas deseadas de hemofiltración. Ambos animales sobrevivieron. Como complicación se registró hematuria en un caso. Conclusión: El modelo animal elegido, para el entrenamiento en el manejo de ECMO, fue satisfactorio.