| Literature DB >> 33510735 |
Qiang Zhang1, Qian Shao1, Yaqiong Guo2, Na Li2, Yu Li3, Jiayuan Su1, Rui Xu1, Ziding Zhang3, Lihua Xiao2, Yaoyu Feng1,2.
Abstract
In Cryptosporidium spp., calcium-dependent protein kinases (CDPKs) are considered promising targets for the development of pharmaceutical interventions. Whole-genome sequencing has revealed the presence of 11 CDPKs in Cryptosporidium parvum (CpCDPKs). In this study, we expressed recombinant CpCDPK4, CpCDPK5, and CpCDPK6 in Escherichia coli. The biological characteristics and functions of these CpCDPKs were examined by using quantitative reverse transcription PCR (qRT-PCR), immunofluorescence microscopy, and an in vitro neutralization assay. The expression of the CpCDPK4 gene peaked at 12 h post-infection, the CpCDPK5 gene peaked at 12 and 48 h, and the CpCDPK6 gene peaked at 2-6 h. CpCDPK4 protein was located in the anterior and mid-anterior regions of sporozoites, and CpCDPK5 protein was located over the entire sporozoites, while CpCDPK6 protein was expressed in a spotty pattern. Immune sera of CpCDPK4 and CpCDPK6 exhibited significant inhibitory effects on host cell invasion, while the immune sera of CpCDPK5 had no effects. These differences in protein localization, gene expressions, and neutralizing capacities indicated that the CpCDPK proteins may have different roles during the lifecycle of Cryptosporidium spp.Entities:
Keywords: Cryptosporidium parvum; calcium-dependent protein kinase; inhibitor; intracellular development; invasion
Year: 2021 PMID: 33510735 PMCID: PMC7835281 DOI: 10.3389/fmicb.2020.622203
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640