2015
DOI: 10.1590/1519-6984.0313
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Adenoviruses of canine and human origins in stool samples from free-living pampas foxes (<italic>Lycalopex gymnocercus</italic>) and crab-eating foxes (<italic>Cerdocyon thous</italic>) in São Francisco de Paula, Rio dos Sinos basin

Abstract: The spread of enteric viruses of domestic animals and human beings to wild species can be facilitated by the resistance of these viruses on the environment and their ability to be transmitted by water and contaminated food. The health status of the populations of pampas foxes (Lycalopex gymnocercus) and crab-eating foxes (Cerdocyon thous) is largely unknown and the landscapes occupied by these animals in southern Brazil have been threatened by human occupation and expansion of agriculture. In this work, the se… Show more

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Cited by 17 publications
(5 citation statements)
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“…One study by our team has reported these infections in the city of São Francisco de Paula, Rio Grande do Sul. That study detected HAdV DNA in 82.3% (14/17) of stools samples and CAdV in five specimens [20]. In addition, enteric viruses can be easily spread from humans to domestic animals due to the non-enveloped virus environmental resistance and its capacity to spread by contaminated feeds.…”
Section: Discussionmentioning
confidence: 78%
See 1 more Smart Citation
“…One study by our team has reported these infections in the city of São Francisco de Paula, Rio Grande do Sul. That study detected HAdV DNA in 82.3% (14/17) of stools samples and CAdV in five specimens [20]. In addition, enteric viruses can be easily spread from humans to domestic animals due to the non-enveloped virus environmental resistance and its capacity to spread by contaminated feeds.…”
Section: Discussionmentioning
confidence: 78%
“…For detection of CAdV-A a set of primers, which had the hexon protein as the target gene, was used. The forward was CAV-F1 5´-CACGATGT-GACCACTGAGAG-3´ and the reverse was CAV-R1 5´-GGTAGGTATTGTTTGTGACAGC-3' [20]. The final volume of the reaction was 50 µL: 25 µL from Mix at PCR solution 3 , 18 µL of water RNAse and DNAse free, 20 pmol of each primer 3 , and 5 µL of DNA (at approximately 100 ng/µL).…”
Section: Viral Analysismentioning
confidence: 99%
“…Polymerase chain reaction (PCR) was used for detecting viral genomes: reactions were made in a final volume of 50 µL, being 5 µL of DNA sample, 25 µL of the PCR Mix solution (Promega ® , Madison, USA), 18 µL of RNA-DNAse free water and 1 µl of each primer. CAdV-A amplification started with an initial denaturation step of 98 ºC for 7 min, followed by 35 cycles of 1 min at 94 ºC, 1 min at 54 ºC and 1 min at 72 ºC, and a final extension of 7 min at 72 ºC 14 . CPV-1 amplification started with an initial denaturation step started at 95 ºC for 5 min followed by 35 cycles of 30 s at 95 ºC, 30 s at 50 ºC and 1 min at 72 ºC, followed by a final extension step of 7 min at 72 ºC 15 .…”
Section: Methodsmentioning
confidence: 99%
“…The amplicon resulted 300 to 350 bp of the gene encoding a CAV-1 and CAV-2 hexon protein, respectively [30].…”
Section: Polymerase Chain Reactionmentioning
confidence: 99%