PUBLICATION
Molecular characterization and expression analysis of two peptidoglycan recognition proteins (CcPGRP5, CcPGRP6) in larvae ontogeny of common carp Cyprinus carpio L. and upon immune stimulation by bacteria
- Authors
- Zhang, F., Shan, S., Xu, X., Wang, Y., Zhang, Y., Yin, M., Yang, G.
- ID
- ZDB-PUB-190108-1
- Date
- 2019
- Source
- BMC veterinary research 15: 10 (Journal)
- Registered Authors
- Keywords
- Aeromonas hydrophila, Common carp, Larva, PGRP
- MeSH Terms
-
- Aeromonas hydrophila/immunology
- Animals
- Carps/genetics
- Carps/immunology*
- Carps/microbiology
- Carrier Proteins/genetics*
- Carrier Proteins/immunology
- Carrier Proteins/metabolism
- Fish Proteins/genetics*
- Fish Proteins/immunology
- Fish Proteins/metabolism
- Immunity, Innate/genetics
- Immunity, Innate/immunology
- Larva/immunology
- Larva/metabolism
- Phylogeny
- Sequence Alignment/veterinary
- Sequence Analysis, DNA/veterinary
- Transcriptome
- PubMed
- 30612570 Full text @ BMC Vet. Res.
Citation
Zhang, F., Shan, S., Xu, X., Wang, Y., Zhang, Y., Yin, M., Yang, G. (2019) Molecular characterization and expression analysis of two peptidoglycan recognition proteins (CcPGRP5, CcPGRP6) in larvae ontogeny of common carp Cyprinus carpio L. and upon immune stimulation by bacteria. BMC veterinary research. 15:10.
Abstract
Background Although teleost fish developed acquired immunity firstly in evolution, innate immunity is still very important for them. Innate immunity depends on pattern recognition receptors (PRRs) to distinguish "self" and "non-self", Peptidoglycan (PGN) recognition protein (PGRP) is one of the receptors and it can bind to multiple components of bacterial envelope.
Results We report the cloning and expression analysis of two PGRPs (Ccpgrp5 and Ccpgrp6) from common carp (Cyprinus carpio L). The Ccpgrp5 gene encodes a protein of 199 amino acid (aa) with PGRP domain, Ami_2 domain and four Zn2+ binding sites required for amidase activity, but without signal peptide and transmembrane domain. The Ccpgrp6 gene encodes a protein of 446 aa with PGRP domain, Ami_2 domain, signal peptide, five Zn2+ binding sites required for amidase activity and two sites for N-glycosylation. The phylogenetic analysis revealed that the CcPGRP5 and CcPGRP6 are closely related to Ctenopharyngodon idella and Danio rerio. Ccpgrp5 and Ccpgrp6 were expressed in all tissues examined including liver, spleen, muscle, oral epithelium, head kidney, gill, skin, gonad, brain, foregut and hindgut and showed different distribution characteristics. During the embryonic and early larval developmental stages of common carp, Ccpgrp6 was detected to be highly expressed at 10 days post fertilization(dpf) and 36 dpf, while Ccpgrp5 were hardly detected using Real-time quantitative PCR. After being challenged with Aeromonas hydrophila, Ccpgrp5 in adult common carp was induced and up-regulated in all the tissues, especially in gill and spleen, but not in head kidney, while Ccpgrp6 was up-regulated in all the tissues, especially in liver, head kidney and gill. The varied expression profiling of Ccpgrp5 and Ccpgrp6 indicated they had different roles in the host immune response.
Conclusions These results indicated the two PGRPs, especially Ccpgrp6, played an important role in the immune defense of common carp during larva development and against Aeromonas hydrophila, providing insight to further exploration of protecting fish against bacteria infectious disease.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping