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1.
PLoS One ; 11(3): e0151921, 2016.
Article in English | MEDLINE | ID: mdl-26986573

ABSTRACT

The Brazilian South coast seasonally hosts numerous marine species, observed particularly during winter months. Some animals, including fur seals, are found dead or debilitated along the shore and may harbor potential pathogens within their microbiota. In the present study, a metagenomic approach was performed to evaluate the viral diversity in feces of fur seals found deceased along the coast of the state of Rio Grande do Sul. The fecal virome of two fur seal species was characterized: the South American fur seal (Arctocephalus australis) and the Subantarctic fur seal (Arctocephalus tropicalis). Fecal samples from 10 specimens (A. australis, n = 5; A. tropicalis, n = 5) were collected and viral particles were purified, extracted and amplified with a random PCR. The products were sequenced through Ion Torrent and Illumina platforms and assembled reads were submitted to BLASTx searches. Both viromes were dominated by bacteriophages and included a number of potentially novel virus genomes. Sequences of picobirnaviruses, picornaviruses and a hepevirus-like were identified in A. australis. A rotavirus related to group C, a novel member of the Sakobuvirus and a sapovirus very similar to California sea lion sapovirus 1 were found in A. tropicalis. Additionally, sequences of members of the Anelloviridae and Parvoviridae families were detected in both fur seal species. This is the first metagenomic study to screen the fecal virome of fur seals, contributing to a better understanding of the complexity of the viral community present in the intestinal microbiota of these animals.


Subject(s)
Fur Seals/virology , Metagenomics , Viruses/genetics , Anelloviridae/genetics , Animals , Bacteriophages/genetics , Base Sequence , Feces/virology , Genome, Viral/genetics , Genomic Library , Herpesviridae/genetics , Molecular Sequence Data , Parvoviridae/genetics , Phylogeny , Picobirnavirus/genetics , Picornaviridae/genetics , Rotavirus/genetics , Sapovirus/genetics
2.
J Hered ; 106 Suppl 1: 503-11, 2015.
Article in English | MEDLINE | ID: mdl-26245785

ABSTRACT

Habitat loss and fragmentation are important threats to carnivores worldwide, and can be especially intense for large predators. Jaguars have already been extirpated from over half of their original area of distribution, and few regions still maintain large populations. For these, detailed understanding is crucial for setting appropriate recovery targets in impacted areas. The Pantanal is among the best examples of a region with a large jaguar population in a healthy environment. Here, we analyzed 12 microsatellite loci to characterize genetic diversity and population structure of 52 jaguars sampled in 4 localities of the southern Pantanal, and compared them with prior studies of heavily fragmented populations of the Atlantic Forest. Although we observed some internal structure among the Pantanal localities, our results indicated that this area comprises a single population with high genetic variability. Moreover, our comparative analyses supported the hypothesis that the strong population structure observed in the Atlantic Forest derives from recent, anthropogenic fragmentation. We also observed significant but low levels of genetic differentiation between the Pantanal and Atlantic Forest populations, indicating recent connectivity between jaguars occurring in these biomes. Evidence for admixture between the Pantanal and a population on the western boundary of the Atlantic Forest corroborates the transitional nature of the latter area, where the jaguar population has already been extirpated. Our results can be used to understand jaguar population dynamics in a region that is less disturbed than the Atlantic forest, and to support the design of conservation strategies that maintain and restore natural connectivity among currently isolated areas.


Subject(s)
Genetic Variation , Genetics, Population , Panthera/genetics , Animals , Bayes Theorem , Brazil , Conservation of Natural Resources , Ecosystem , Genotype , Microsatellite Repeats , Population Dynamics , Sequence Analysis, DNA
3.
Acta Trop ; 131: 1-10, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24291677

ABSTRACT

A 3-year ecological study of small mammals was carried out in an endemic area for hantavirus pulmonary syndrome in the state of Santa Catarina in Southern Brazil. A total of 994 rodents of 14 different species corresponding to the subfamilies of Sigmodontinae, Murinae, Eumysopinae, and Caviinae were captured during 2004-2006. Oligoryzomys nigripes and Akodon montensis were the most abundant species and showed a clear seasonal pattern with higher population sizes during the winter. Rodent population outbreaks, associated within bamboo mast seeding events, were detected predominantly in areas where hantavirus pulmonary syndrome cases were notified in the state. Antibody reactivity to Hantavirus was detected in five sigmodontine species: O. nigripes (39/435), A. montensis (15/318), Akodon paranaensis (4/37), Thaptomys nigrita (1/86) and Sooretamys angouya (1/12). The highest hantavirus antibody prevalence occurred during the period of highest population size in A. montensis. For O. nigripes, hantavirus prevalence was higher in late spring, when reproduction was more frequent. Co-circulation of Juquitiba (JUQV) and Jabora (JABV) viruses was observed - JABV in A. paranaensis and A. montensis; JUQV in O. nigripes and T. nigrita. JABV occurrence was associated to gender and population size of the rodent while JUQV was related to gender, season, temperature, and locality.


Subject(s)
Antibodies, Viral/blood , Hantavirus Infections/veterinary , Hantavirus Pulmonary Syndrome/epidemiology , Orthohantavirus/isolation & purification , Rodent Diseases , Rodentia/virology , Animals , Brazil/epidemiology , Female , Orthohantavirus/classification , Orthohantavirus/immunology , Hantavirus Infections/epidemiology , Hantavirus Infections/virology , Hantavirus Pulmonary Syndrome/virology , Humans , Male , Population Dynamics , Prevalence , Seasons , Sex Factors
4.
Mol Ecol Resour ; 11(5): 862-71, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21676206

ABSTRACT

The use of scat surveys to obtain DNA has been well documented in temperate areas, where DNA preservation may be more effective than in tropical forests. Samples obtained in the tropics are often exposed to high humidity, warm temperatures, frequent rain and intense sunlight, all of which can rapidly degrade DNA. Despite these potential problems, we demonstrate successful mtDNA amplification and sequencing for faeces of carnivores collected in tropical conditions and quantify how sample condition and environmental variables influence the success of PCR amplification and species identification. Additionally, the feasibility of genotyping nuclear microsatellites from jaguar (Panthera onca) faeces was investigated. From October 2007 to December 2008, 93 faecal samples were collected in the southern Brazilian Amazon. A total of eight carnivore species was successfully identified from 71% of all samples obtained. Information theoretic analysis revealed that the number of PCR attempts before a successful sequence was an important negative predictor across all three responses (success of species identification, success of species identification from the first sequence and PCR amplification success), whereas the relative importance of the other three predictors (sample condition, season and distance from forest edge) varied between the three responses. Nuclear microsatellite amplification from jaguar faeces had lower success rates (15-44%) compared with those of the mtDNA marker. Our results show that DNA obtained from faecal samples works efficiently for carnivore species identification in the Amazon forest and also shows potential for nuclear DNA analysis, thus providing a valuable tool for genetic, ecological and conservation studies.


Subject(s)
Carnivora/genetics , DNA, Mitochondrial/isolation & purification , Feces/chemistry , Nucleic Acid Amplification Techniques/methods , Animals , Brazil , Cluster Analysis , DNA Primers/genetics , DNA, Mitochondrial/genetics , Genetic Markers/genetics , Microsatellite Repeats/genetics , Phylogeny , Sequence Analysis, DNA/methods , Species Specificity , Tropical Climate
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