2020
DOI: 10.3389/fcimb.2019.00477
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Gene Expression in the Salivary Gland of Rhipicephalus (Boophilus) microplus Fed on Tick-Susceptible and Tick-Resistant Hosts

Abstract: The success of cattle tick fixation largely depends on the secretion of substances that alter the immune response of the host. The majority of these substances are expressed by the parasite salivary gland and secreted in tick saliva. It is known that hosts can mount immune responses against ticks and bovine European breeds, and bovine industrial crossbreeds are more susceptible to infestations than are Bos indicus cattle. To identify candidates for the development of novel control strategies for the cattle tic… Show more

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Cited by 13 publications
(8 citation statements)
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References 129 publications
(171 reference statements)
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“…In ticks, metalloproteases have been found in the midgut, ovary, salivary glands and saliva, where they are particularly abundant and diverse [ 45 , 86 , 97 ]. Tick salivary metalloproteases play functions related to blood-feeding and modulation of the host defensive responses, including degradation of extracellular matrix proteins at the bite site to form the feeding pool and degradation of fibrinogen and fibrin, thereby preventing blood coagulation, degradation of inflammatory mediators and inhibition of host tissue repair via anti-angiogenic activity [ 41 , 92 , 97 99 ]. Not surprisingly, metalloproteases were the enzyme class most abundantly represented in the O. erraticus sialotranscriptome (338 transcripts) (Table 4 ), in parallel with that also reported for other tick sialomes [ 29 , 39 , 41 , 43 , 93 , 98 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In ticks, metalloproteases have been found in the midgut, ovary, salivary glands and saliva, where they are particularly abundant and diverse [ 45 , 86 , 97 ]. Tick salivary metalloproteases play functions related to blood-feeding and modulation of the host defensive responses, including degradation of extracellular matrix proteins at the bite site to form the feeding pool and degradation of fibrinogen and fibrin, thereby preventing blood coagulation, degradation of inflammatory mediators and inhibition of host tissue repair via anti-angiogenic activity [ 41 , 92 , 97 99 ]. Not surprisingly, metalloproteases were the enzyme class most abundantly represented in the O. erraticus sialotranscriptome (338 transcripts) (Table 4 ), in parallel with that also reported for other tick sialomes [ 29 , 39 , 41 , 43 , 93 , 98 ].…”
Section: Resultsmentioning
confidence: 99%
“…The family of TIL-domain inhibitors includes chymotrypsin, elastase and trypsin inhibitors, which are ubiquitous in blood-feeding insects and tick sialomes. Some members of this family are known to interfere with the host inflammatory response and others have been characterised as antimicrobial peptides [ 99 ]. Kazal domain inhibitors are less frequent in tick sialomes and their function remains unknown [ 45 , 109 ].…”
Section: Resultsmentioning
confidence: 99%
“…Giachetto et al ( 2020 ) generated salivary gland transcriptomes for engorged female R. microplus that was fed on tick-resistant or tick-susceptible hosts. The transcriptome was assembled from 74,639,552 reads (holstein cattle) and 63,013,658 reads (crossbreed cattle) resulting in 235,451 contigs.…”
Section: Complexity Measured By Next-generation Sequencing Of Transcrmentioning
confidence: 99%
“…Proteins containing a reeler domain were described in a manifold of studies involved in the tick’s innate immunity. Previous investigations indicate the participation of this protein in the Bombyx mori melanization cascade, and it is also reported as a defense response against the viruses in whiteflies of the Bemisia tabaci species complex [ 49 , 50 ]. Apart from insects, there is a study reporting protein with a reeler domain favoring the colonization of Borrelia burgdorferi in gut cells of Ixodes scapularis [ 51 ].…”
Section: Discussionmentioning
confidence: 99%