High-throughput metagenome analysis of the Sarcoptes scabiei internal microbiota and in-situ identification of intestinal Streptomyces sp
Multiple parasitic arthropods of medical importance depend on symbiotic bacteria. While the link between scabies and secondary bacterial infections causing post infective complications of Group A streptococcal and staphylococcal pyoderma is increasingly recognized, very little is known about the mic...
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Veröffentlicht in: | Scientific reports 2019-08, Vol.9 (1), p.11744-11, Article 11744 |
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Sprache: | eng |
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Zusammenfassung: | Multiple parasitic arthropods of medical importance depend on symbiotic bacteria. While the link between scabies and secondary bacterial infections causing post infective complications of Group A streptococcal and staphylococcal pyoderma is increasingly recognized, very little is known about the microbiota of
Sarcoptes scabiei
. Here we analyze adult female mite and egg metagenome datasets. The majority of adult mite bacterial reads matched with Enterobacteriaceae (phylum Proteobacteria), followed by Corynebacteriaceae (phylum Actinobacteria).
Klebsiella
was the most dominant genus (78%) and
Corynebacterium
constituted 9% of the assigned sequences. Scabies mite eggs had a more diverse microbial composition with sequences from Proteobacteria being the most dominant (75%), while Actinobacteria, Bacteroidetes and Firmicutes accounted for 23% of the egg microbiome sequences. DNA sequences of a potential endosymbiont, namely
Streptomyces
, were identified in the metagenome sequence data of both life stages. The presence of
Streptomyces
was confirmed by conventional PCR. Digital droplet PCR indicated higher
Streptomyces
numbers in adult mites compared to eggs.
Streptomyces
were localized histologically in the scabies mite gut and faecal pellets by Fluorescent
In Situ
Hybridization (FISH).
Streptomyces
may have essential symbiotic roles in the scabies parasite intestinal system requiring further investigation. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-019-47892-0 |