TY - JOUR
T1 - Litopenaeus vannamei stylicins are constitutively produced by hemocytes and intestinal cells and are differentially modulated upon infections
AU - Farias, Natanael Dantas
AU - Falchetti, Marcelo
AU - Matos, Gabriel Machado
AU - Schmitt, Paulina
AU - Barreto, Cairé
AU - Argenta, Nicolas
AU - Rolland, Jean Luc
AU - Bachère, Evelyne
AU - Perazzolo, Luciane Maria
AU - Rosa, Rafael Diego
N1 - Funding Information:
We are grateful to the Laboratory of Marine Shrimp (Federal University of Santa Catarina - UFSC) for providing the shrimp used in this study and to Fabio S Ribeiro for his technical assistance in the whole-mount immunofluorescence experiments. The authors are also thankful to the Electronic Microscopy Central Laboratory (LCME-UFSC) and the Multiuser Laboratory of Biology Studies (LAMEB-UFSC). This work was supported by the Brazilian funding agencies CNPq (MEC/MCTI/CAPES/CNPq/FAPs PVE 401191/2014-1 and MCTI/CNPq Universal 406530/2016-5) and CAPES (CIMAR 1974/2014). P Schmitt was funded by FONDECYT grant 11150009. ND Farias and GM Matos were supported by scholarships provided by FAPESC while N Argenta received a scholarship provided by CNPq. M Falchetti and C Barreto were supported by fellowships provided by CAPES.
Funding Information:
We are grateful to the Laboratory of Marine Shrimp (Federal University of Santa Catarina - UFSC) for providing the shrimp used in this study and to Fabio S Ribeiro for his technical assistance in the whole-mount immunofluorescence experiments. The authors are also thankful to the Electronic Microscopy Central Laboratory (LCME-UFSC) and the Multiuser Laboratory of Biology Studies (LAMEB-UFSC). This work was supported by the Brazilian funding agencies CNPq ( MEC/MCTI/CAPES/CNPq/FAPs PVE 401191/2014-1 and MCTI/CNPq Universal 406530/2016-5 ) and CAPES ( CIMAR 1974/2014 ). P Schmitt was funded by FONDECYT grant 11150009 . ND Farias and GM Matos were supported by scholarships provided by FAPESC while N Argenta received a scholarship provided by CNPq . M Falchetti and C Barreto were supported by fellowships provided by CAPES .
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2019/3
Y1 - 2019/3
N2 - Stylicins are anionic antimicrobial host defense peptides (AAMPs) composed of a proline-rich N-terminal region and a C-terminal portion containing 13 conserved cysteine residues. Here, we have increased our knowledge about these unexplored crustacean AAMPs by the characterization of novel stylicin members in the most cultivated penaeid shrimp, Litopenaeus vannamei. We showed that the L. vannamei stylicin family is composed of two members (Lvan-Stylicin1 and Lvan-Stylicin2) encoded by different loci which vary in gene copy number. Unlike the other three gene-encoded antimicrobial peptide families from penaeid shrimp, the expression of Lvan-Stylicins is not restricted to hemocytes. Indeed, they are also produced by the columnar epithelial cells lining the midgut and its anterior caecum. Interestingly, Lvan-Stylicins are simultaneously transcribed at different transcriptional levels in a single shrimp and are differentially modulated in hemocytes after infections. While the expression of both genes showed to be responsive to damage-associated molecular patterns, only Lvan-Stylicin2 was induced after a Vibrio infection. Besides, Lvan-Stylicins also showed a distinct pattern of gene expression in the three portions of the midgut (anterior, middle and posterior) and during shrimp development. We provide here the first evidence of the diversity of the stylicin antimicrobial peptide family in terms of sequence and gene expression distribution and regulation.
AB - Stylicins are anionic antimicrobial host defense peptides (AAMPs) composed of a proline-rich N-terminal region and a C-terminal portion containing 13 conserved cysteine residues. Here, we have increased our knowledge about these unexplored crustacean AAMPs by the characterization of novel stylicin members in the most cultivated penaeid shrimp, Litopenaeus vannamei. We showed that the L. vannamei stylicin family is composed of two members (Lvan-Stylicin1 and Lvan-Stylicin2) encoded by different loci which vary in gene copy number. Unlike the other three gene-encoded antimicrobial peptide families from penaeid shrimp, the expression of Lvan-Stylicins is not restricted to hemocytes. Indeed, they are also produced by the columnar epithelial cells lining the midgut and its anterior caecum. Interestingly, Lvan-Stylicins are simultaneously transcribed at different transcriptional levels in a single shrimp and are differentially modulated in hemocytes after infections. While the expression of both genes showed to be responsive to damage-associated molecular patterns, only Lvan-Stylicin2 was induced after a Vibrio infection. Besides, Lvan-Stylicins also showed a distinct pattern of gene expression in the three portions of the midgut (anterior, middle and posterior) and during shrimp development. We provide here the first evidence of the diversity of the stylicin antimicrobial peptide family in terms of sequence and gene expression distribution and regulation.
KW - Antimicrobial peptide
KW - Crustacean
KW - Host defense peptide
KW - Invertebrate immunity
KW - Molecular diversity
KW - Penaeid shrimp
UR - http://www.scopus.com/inward/record.url?scp=85056701436&partnerID=8YFLogxK
U2 - 10.1016/j.fsi.2018.11.021
DO - 10.1016/j.fsi.2018.11.021
M3 - Article
C2 - 30439499
AN - SCOPUS:85056701436
SN - 1050-4648
VL - 86
SP - 82
EP - 92
JO - Fish and Shellfish Immunology
JF - Fish and Shellfish Immunology
ER -