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Insights about echinostomiasis by paleomolecular diagnosis
Institution:1. Universidade Federal Fluminense, Instituto Biomédico, Departamento de Microbiologia e Parasitologia, Laboratório de Biologia Molecular de Parasitos, Rua Professor Hernani Melo 101, São Domingos, Niterói, RJ, CEP 24.210-130, Brazil;2. Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Laboratório de Biologia e Parasitologia de Mamíferos Silvestres Reservatórios, Av. Brasil, 4365, Rio de Janeiro, RJ, CEP 21.045-900, Brazil;3. Laboratório de Paleoparasitologia, Escola Nacional de Saúde Pública-Fundação Oswaldo Cruz, Rua Leopoldo Bulhões 1480, Rio de Janeiro, RJ, CEP 21.041-210, Brazil;1. Semiconductor Physics, Technische Universität Chemnitz, D-09107 Chemnitz, Germany;2. Institute for Print and Media Technology, Technische Universität Chemnitz, D-09107 Chemnitz, Germany;3. Coordination Chemistry, Technische Universität Chemnitz, D-09107 Chemnitz, Germany;4. Inorganic Chemistry, Technische Universität Chemnitz, D-09107 Chemnitz,Germany;5. Solid Surface Analysis, Technische Universität Chemnitz, D-09107 Chemnitz, Germany
Abstract:Echinostomiasis is a zoonosis caused by intestinal trematodes and transmitted by the ingestion of mollusks, crustaceans, fish, amphibians, and reptiles, either raw or poorly cooked. Today human infection is endemic in Southeast Asia and the Far East, but has been reported more recently in other regions of the world. Interestingly eggs identified as Echinostoma sp. were found in coprolites from a mummified body human in Brazil, dated 560 ± 40 BP (before present). However, the specific diagnosis based on morphology of the eggs has not been resolved at the species level. As a follow-up to the previous finding, the current study now aims to standardize the methodology for molecular diagnosis and apply it to the coprolite, using current Echinostoma paraensei-positive feces as the reference, and also the same fecal material dried in a stove as an experimental coprolite model. Isolated eggs of E. paraensei and adult worm were included to verify the sensibility and as positive control, respectively. An adult worm of E. luisreyi was used for comparison. PCR using primers in-house for ITS1 region (126 bp) and cox1 (123 bp) of Echinostoma spp. and subsequent nucleotide sequencing were performed. This is the first molecular paleoparasitological diagnosis for echinostomiasis. The methodology was able to amplify specific DNA fragments for the genus Echinostoma sp. in all samples: adult worm, feces, and a single egg of the parasite, in both the experimental coprolite and archaeological sample. Additionally we observed that ancient DNA can also be retrieved without rehydrating the material. The nucleotide sequences from E. paraensei and E. luisreyi are very similar in the fragment analyzed that difficult the differentiation these species, but DNA sequence analysis recovered in the parasite found in the mummy showed more similarity with the species E. paraensei.
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