4.6 Article

Molecular characterization and expression analysis of annexin B3 and B38 as secretory proteins in Echinococcus granulosus

Journal

PARASITES & VECTORS
Volume 14, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13071-021-04596-7

Keywords

Echinococcus granulosus; Annexin; Calcium ion; Western blotting; Immunofluorescence localization; Secretory protein

Funding

  1. National Natural Science Foundation of China [31672547]
  2. Key Technology R&D Program of Sichuan Province, China [2020YFN0030]

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Cystic echinococcosisis a parasitic zoonotic disease that poses a threat to public health and animal husbandry. Annexins are a family of phospholipid-binding proteins with calcium ion-binding activity. The cloned annexin genes have calcium-binding sites and strong immunoreactivity to serum from infected animals. They are expressed in various stages of the parasite and are found near the hydatid cyst in liver tissues.
BackgroundCystic echinococcosis is a parasitic zoonotic disease, which poses a threat to public health and animal husbandry, and causes significant economic losses. Annexins are a family of phospholipid-binding proteins with calcium ion-binding activity, which have many functions.MethodsTwo annexin protein family genes [Echinococcus granulosus annexin B3 (EgAnxB3) and EgAnxB38] were cloned and molecularly characterized using bioinformatic analysis. The immunoreactivity of recombinant EgAnxB3 (rEgAnxB3) and rEgAnxB38 was investigated using western blotting. The distribution of EgAnxB3 and EgAnxB38 in protoscoleces (PSCs), the germinal layer, 18-day strobilated worms and 45-day adult worms was analyzed by immunofluorescence localization, and their secretory characteristics were analyzed preliminarily; in addition, quantitative real-time reverse transcription polymerase chain reaction was used to analyze their transcript levels in PSCs and 28-day strobilated worms stages. The phospholipid-binding activities of rEgAnxB3 and rEgAnxB38 were also analyzed.ResultsEgAnxB3 and EgAnxB38 are conserved and contain calcium-binding sites. Both rEgAnxB3 and rEgAnxB38 could be specifically recognized by the serum samples from E. granulosus-infected sheep, indicating that they had strong immunoreactivity. EgAnxB3 and EgAnxB38 were distributed in all stages of E. granulosus, and their transcript levels were high in the 28-day strobilated worms. They were found in liver tissues near the cysts. In addition, rEgAnxB3 has Ca2+-dependent phospholipid-binding properties.ConclusionsEgAnxB3 and EgAnxB38 contain calcium-binding sites, and rEgAnxB3 has Ca2+-dependent phospholipid-binding properties. EgAnxB3 and EgAnxB38 were transcribed in PSCs and 28-day strobilated worms. They were expressed in all stages of E. granulosus, and distributed in the liver tissues near the hydatid cyst, indicating that they are secreted proteins that play a crucial role in the development of E. granulosus.

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