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Tick salivary gland transcriptomics and proteomics
LA. Martins, C. Bensaoud, J. Kotál, J. Chmelař, M. Kotsyfakis
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
NLK
Free Medical Journals
from 1997 to 1 year ago
Medline Complete (EBSCOhost)
from 1998-01-01 to 1 year ago
Wiley Free Content
from 1997 to 1 year ago
PubMed
33135186
DOI
10.1111/pim.12807
Knihovny.cz E-resources
- MeSH
- Genome physiology MeSH
- Host-Pathogen Interactions MeSH
- Ticks genetics physiology MeSH
- Humans MeSH
- Proteomics * MeSH
- Salivary Glands physiology MeSH
- Transcriptome physiology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
'Omics' technologies have facilitated the identification of hundreds to thousands of tick molecules that mediate tick feeding and play a role in the transmission of tick-borne diseases. Deep sequencing methodologies have played a key role in this knowledge accumulation, profoundly facilitating the study of the biology of disease vectors lacking reference genomes. For example, the nucleotide sequences of the entire set of tick salivary effectors, the so-called tick 'sialome', now contain at least one order of magnitude more transcript sequences compared to similar projects based on Sanger sequencing. Tick feeding is a complex and dynamic process, and while the dynamic 'sialome' is thought to mediate tick feeding success, exactly how transcriptome dynamics relate to tick-host-pathogen interactions is still largely unknown. The identification and, importantly, the functional analysis of the tick 'sialome' is expected to shed light on this 'black box'. This information will be crucial for developing strategies to block pathogen transmission, not only for anti-tick vaccine development but also the discovery and development of new, pharmacologically active compounds for human diseases.
References provided by Crossref.org
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