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Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy
Genital mycoplasmas, including Ureaplasma spp., are among the smallest human pathogenic bacteria and are associated with preterm birth. Electron microscopic observation of U. parvum showed that these prokaryotes have a regular, spherical shape with a mean diameter of 146 nm. U. parvum was internaliz...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458467/ https://www.ncbi.nlm.nih.gov/pubmed/28088841 http://dx.doi.org/10.1002/mbo3.441 |
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author | Nishiumi, Fumiko Ogawa, Michinaga Nakura, Yukiko Hamada, Yusuke Nakayama, Masahiro Mitobe, Jiro Hiraide, Atsushi Sakai, Norio Takeuchi, Makoto Yoshimori, Tamotsu Yanagihara, Itaru |
author_facet | Nishiumi, Fumiko Ogawa, Michinaga Nakura, Yukiko Hamada, Yusuke Nakayama, Masahiro Mitobe, Jiro Hiraide, Atsushi Sakai, Norio Takeuchi, Makoto Yoshimori, Tamotsu Yanagihara, Itaru |
author_sort | Nishiumi, Fumiko |
collection | PubMed |
description | Genital mycoplasmas, including Ureaplasma spp., are among the smallest human pathogenic bacteria and are associated with preterm birth. Electron microscopic observation of U. parvum showed that these prokaryotes have a regular, spherical shape with a mean diameter of 146 nm. U. parvum was internalized into HeLa cells by clathrin‐mediated endocytosis and survived for at least 14 days around the perinuclear region. Intracellular U. parvum reached endosomes in HeLa cells labeled with EEA1, Rab7, and LAMP‐1 within 1 to 3 hr. After 3 hr of infection, U. parvum induced the cytosolic accumulation of galectin‐3 and was subsequently entrapped by the autophagy marker LC3. However, when using atg7 (−/−) MEF cells, autophagy was inadequate for the complete elimination of U. parvum in HeLa cells. U. parvum also colocalized with the recycling endosome marker Rab11. Furthermore, the exosomes purified from infected HeLa cell culture medium included U. parvum. In these purified exosomes ureaplasma lipoprotein multiple banded antigen, host cellular annexin A2, CD9, and CD63 were detected. This research has successfully shown that Ureaplasma spp. utilize the host cellular membrane compartments possibly to evade the host immune system. |
format | Online Article Text |
id | pubmed-5458467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54584672017-06-06 Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy Nishiumi, Fumiko Ogawa, Michinaga Nakura, Yukiko Hamada, Yusuke Nakayama, Masahiro Mitobe, Jiro Hiraide, Atsushi Sakai, Norio Takeuchi, Makoto Yoshimori, Tamotsu Yanagihara, Itaru Microbiologyopen Original Research Genital mycoplasmas, including Ureaplasma spp., are among the smallest human pathogenic bacteria and are associated with preterm birth. Electron microscopic observation of U. parvum showed that these prokaryotes have a regular, spherical shape with a mean diameter of 146 nm. U. parvum was internalized into HeLa cells by clathrin‐mediated endocytosis and survived for at least 14 days around the perinuclear region. Intracellular U. parvum reached endosomes in HeLa cells labeled with EEA1, Rab7, and LAMP‐1 within 1 to 3 hr. After 3 hr of infection, U. parvum induced the cytosolic accumulation of galectin‐3 and was subsequently entrapped by the autophagy marker LC3. However, when using atg7 (−/−) MEF cells, autophagy was inadequate for the complete elimination of U. parvum in HeLa cells. U. parvum also colocalized with the recycling endosome marker Rab11. Furthermore, the exosomes purified from infected HeLa cell culture medium included U. parvum. In these purified exosomes ureaplasma lipoprotein multiple banded antigen, host cellular annexin A2, CD9, and CD63 were detected. This research has successfully shown that Ureaplasma spp. utilize the host cellular membrane compartments possibly to evade the host immune system. John Wiley and Sons Inc. 2017-01-15 /pmc/articles/PMC5458467/ /pubmed/28088841 http://dx.doi.org/10.1002/mbo3.441 Text en © 2017 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Nishiumi, Fumiko Ogawa, Michinaga Nakura, Yukiko Hamada, Yusuke Nakayama, Masahiro Mitobe, Jiro Hiraide, Atsushi Sakai, Norio Takeuchi, Makoto Yoshimori, Tamotsu Yanagihara, Itaru Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy |
title | Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy |
title_full | Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy |
title_fullStr | Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy |
title_full_unstemmed | Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy |
title_short | Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy |
title_sort | intracellular fate of ureaplasma parvum entrapped by host cellular autophagy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458467/ https://www.ncbi.nlm.nih.gov/pubmed/28088841 http://dx.doi.org/10.1002/mbo3.441 |
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