Abstract

Background: Neospora caninum is an apicomplexan parasite that infects many mammals and particularly causes abortion in cattle. The key factors in its wide distribution are its virulence and ability to transform between tachyzoite and bradyzoite forms. However, the factors are not well understood. Although Puf protein (named after Pumilio from Drosophila melanogaster and fem-3 binding factor from Caenorhabditis elegans) have a functionally conserved role in promoting proliferation and inhibiting differentiation in many eukaryotes, the function of the Puf proteins in N. caninum is poorly understood. Methods: The CRISPR/CAS9 system was used to identify and study the function of the Puf protein in N. caninum. Results: We showed that N. caninum encodes a Puf protein, which was designated NcPuf1. NcPuf1 is found in the cytoplasm in intracellular parasites and in processing bodies (P-bodies), which are reported for the first time in N. caninum in extracellular parasites. NcPuf1 is not needed for the formation of P-bodies in N. caninum. The deletion of NcPuf1 (ΔNcPuf1) does not affect the differentiation in vitro and tissue cysts formation in the mouse brain. However, ΔNcPuf1 resulted in decreases in the proliferative capacity of N. caninum in vitro and virulence in mice. Conclusions: Altogether, the disruption of NcPuf1 does not affect bradyzoites differentiation, but seriously impairs tachyzoite proliferation in vitro and virulence in mice. These results can provide a theoretical basis for the development of attenuated vaccines to prevent the infection of N. caninum.

Highlights

  • Neospora caninum is an apicomplexan protozoan parasite that is closely related to Toxoplasma gondii.N. caninum does not infect humans [1]

  • Similar to T. gondii, N. caninum tachyzoites can differentiate into bradyzoites that cause chronic infections, which is asymptomatic in immunocompetent hosts

  • NcPuf1 is found in the cytoplasm in intracellular parasites and in P-bodies, which are reported for the first time in N. caninum in extracellular parasites

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Summary

Introduction

Neospora caninum is an apicomplexan protozoan parasite that is closely related to Toxoplasma gondii. Similar to T. gondii, N. caninum tachyzoites can differentiate into bradyzoites that cause chronic infections, which is asymptomatic in immunocompetent hosts. The expression of many genes is altered in the tachyzoite-to-bradyzoite differentiation [6,7]. RNA-binding protein (RBP) is vital for posttranscriptional gene regulation by RNA metabolism [8]. Some Puf proteins can be recruited into ribonucleoprotein (RNP) granules to control target mRNA’s fate under stress. Puf proteins have various functions, they play a functionally conserved role in promoting proliferation and inhibiting differentiation [9]. We showed that N. caninum encodes a Puf protein named NcPuf. The deletion of NcPuf1(∆NcPuf1) does not affect the formation of P-bodies in N. caninum and the differentiation in vitro and tissue cysts formation in the mouse brain. ∆NcPuf resulted in decreases in the proliferative capacity of N. caninum in vitro and virulence in mice

Cell and Parasite Culture
Western Blotting Assay and Immunofluorescence Assays
Quantitative Real-Time PCR
Plaque Assay and Parasite Intracellular Replication Assay
Bradyzoite Differentiation Assay In Vitro
Animal Infection Experiments
Statistical
NcPuf1
NcPuf1 Knockout and Complementary Strains
Identification
NcPuf1 Is Vital for Parasite Growth in Vitro and Virulence in Mice
Conclusions
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