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Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins

Cryptosporidium parvum and Cryptosporidium hominis share highly similar proteomes, with merely ~3% divergence in overall nucleotide sequences. Cryptosporidium-specific MEDLE family is one of the major differences in gene content between the two species. Comparative genomic analysis indicated that ME...

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Autores principales: Su, Jiayuan, Jin, Chanchan, Wu, Haizhen, Fei, Jilan, Li, Na, Guo, Yaqiong, Feng, Yaoyu, Xiao, Lihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549896/
https://www.ncbi.nlm.nih.gov/pubmed/31191495
http://dx.doi.org/10.3389/fmicb.2019.01177
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author Su, Jiayuan
Jin, Chanchan
Wu, Haizhen
Fei, Jilan
Li, Na
Guo, Yaqiong
Feng, Yaoyu
Xiao, Lihua
author_facet Su, Jiayuan
Jin, Chanchan
Wu, Haizhen
Fei, Jilan
Li, Na
Guo, Yaqiong
Feng, Yaoyu
Xiao, Lihua
author_sort Su, Jiayuan
collection PubMed
description Cryptosporidium parvum and Cryptosporidium hominis share highly similar proteomes, with merely ~3% divergence in overall nucleotide sequences. Cryptosporidium-specific MEDLE family is one of the major differences in gene content between the two species. Comparative genomic analysis indicated that MEDLE family may contribute to differences in host range among Cryptosporidium spp. Previous studies have suggested that CpMEDLE-1 encoded by cgd5_4580 and CpMEDLE-2 encoded by cgd5_4590 are potentially involved in the invasion of C. parvum. In this study, we expressed in Escherichia coli, the C. hominis-specific member of the MEDLE protein family, ChMEDLE-1 encoded by chro.50507, and two C. parvum-specific members, CpMEDLE-3 encoded by cgd5_4600 and CpMEDLE-5 encoded by cgd6_5480. Quantitative PCR, immunofluorescence staining and in vitro neutralization assay were conducted to assess their biologic characteristics. The expression of the cgd5_4600 gene was high during 12–48 h of the in vitro culture, while the expression of cgd6_5480 was the highest at 2 h. ChMEDLE-1 and CpMEDLE-3 proteins were mostly located in the anterior and mid-anterior region of sporozoites and merozoites, whereas CpMEDLE-5 was expressed over the entire surface of these invasive stages. Polyclonal antibodies against MEDLE proteins had different neutralization efficiency, reaching approximately 50% for ChMEDLE-1 and 60% for CpMEDLE-3, but only 20% for CpMEDLE-5. The differences in protein and gene expression and neutralizing capacity indicated the MEDLE proteins may have different roles during Cryptosporidium invasion and growth.
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spelling pubmed-65498962019-06-12 Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins Su, Jiayuan Jin, Chanchan Wu, Haizhen Fei, Jilan Li, Na Guo, Yaqiong Feng, Yaoyu Xiao, Lihua Front Microbiol Microbiology Cryptosporidium parvum and Cryptosporidium hominis share highly similar proteomes, with merely ~3% divergence in overall nucleotide sequences. Cryptosporidium-specific MEDLE family is one of the major differences in gene content between the two species. Comparative genomic analysis indicated that MEDLE family may contribute to differences in host range among Cryptosporidium spp. Previous studies have suggested that CpMEDLE-1 encoded by cgd5_4580 and CpMEDLE-2 encoded by cgd5_4590 are potentially involved in the invasion of C. parvum. In this study, we expressed in Escherichia coli, the C. hominis-specific member of the MEDLE protein family, ChMEDLE-1 encoded by chro.50507, and two C. parvum-specific members, CpMEDLE-3 encoded by cgd5_4600 and CpMEDLE-5 encoded by cgd6_5480. Quantitative PCR, immunofluorescence staining and in vitro neutralization assay were conducted to assess their biologic characteristics. The expression of the cgd5_4600 gene was high during 12–48 h of the in vitro culture, while the expression of cgd6_5480 was the highest at 2 h. ChMEDLE-1 and CpMEDLE-3 proteins were mostly located in the anterior and mid-anterior region of sporozoites and merozoites, whereas CpMEDLE-5 was expressed over the entire surface of these invasive stages. Polyclonal antibodies against MEDLE proteins had different neutralization efficiency, reaching approximately 50% for ChMEDLE-1 and 60% for CpMEDLE-3, but only 20% for CpMEDLE-5. The differences in protein and gene expression and neutralizing capacity indicated the MEDLE proteins may have different roles during Cryptosporidium invasion and growth. Frontiers Media S.A. 2019-05-29 /pmc/articles/PMC6549896/ /pubmed/31191495 http://dx.doi.org/10.3389/fmicb.2019.01177 Text en Copyright © 2019 Su, Jin, Wu, Fei, Li, Guo, Feng and Xiao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Su, Jiayuan
Jin, Chanchan
Wu, Haizhen
Fei, Jilan
Li, Na
Guo, Yaqiong
Feng, Yaoyu
Xiao, Lihua
Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins
title Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins
title_full Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins
title_fullStr Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins
title_full_unstemmed Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins
title_short Differential Expression of Three Cryptosporidium Species-Specific MEDLE Proteins
title_sort differential expression of three cryptosporidium species-specific medle proteins
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549896/
https://www.ncbi.nlm.nih.gov/pubmed/31191495
http://dx.doi.org/10.3389/fmicb.2019.01177
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