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Isolation and propagation of leptospires at 37 °C directly from the mammalian host
The causative agent of leptospirosis includes multiple serovars and species of pathogenic leptospires that are excreted via urine from reservoir hosts of infection. Primary isolation takes weeks to months, and is limited to semi-solid media at 28–30 °C. Here we present an alternative media formulati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296004/ https://www.ncbi.nlm.nih.gov/pubmed/32541841 http://dx.doi.org/10.1038/s41598-020-66526-4 |
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author | Hornsby, Richard L. Alt, David P. Nally, Jarlath E. |
author_facet | Hornsby, Richard L. Alt, David P. Nally, Jarlath E. |
author_sort | Hornsby, Richard L. |
collection | PubMed |
description | The causative agent of leptospirosis includes multiple serovars and species of pathogenic leptospires that are excreted via urine from reservoir hosts of infection. Primary isolation takes weeks to months, and is limited to semi-solid media at 28–30 °C. Here we present an alternative media formulation, HAN, compared to commercially available EMJH and the more specialized T80/40/LH media formulations, in semi-solid and liquid compositions, for the primary isolation of two diverse species and serovars of pathogenic leptospires directly from host kidney tissue. All three media types supported the isolation and propagation of L. interrogans serovar Copenhageni strain IC:20:001 in semi-solid media at 29 °C. However, only HAN and T80/40/LH supported the growth of L. borgpetersenii serovar Hardjo strain HB15B203 at 29 °C. In addition, HAN supported primary isolation at 37 °C. Both T80/40/LH and HAN supported primary isolation of strain IC:20:001 in liquid media at 29 °C but only HAN supported growth of strain HB15B203 in liquid media, at both 29 and 37 °C. HAN media supports the primary isolation of fastidious pathogenic leptospires directly from infected host tissue at either 29 or 37 °C: this formulation represents a more defined media for the continued optimization of growth factors required to support the primary isolation of the large and diverse range of species and serovars within the genus Leptospira circulating within domestic and wild animal populations. |
format | Online Article Text |
id | pubmed-7296004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72960042020-06-17 Isolation and propagation of leptospires at 37 °C directly from the mammalian host Hornsby, Richard L. Alt, David P. Nally, Jarlath E. Sci Rep Article The causative agent of leptospirosis includes multiple serovars and species of pathogenic leptospires that are excreted via urine from reservoir hosts of infection. Primary isolation takes weeks to months, and is limited to semi-solid media at 28–30 °C. Here we present an alternative media formulation, HAN, compared to commercially available EMJH and the more specialized T80/40/LH media formulations, in semi-solid and liquid compositions, for the primary isolation of two diverse species and serovars of pathogenic leptospires directly from host kidney tissue. All three media types supported the isolation and propagation of L. interrogans serovar Copenhageni strain IC:20:001 in semi-solid media at 29 °C. However, only HAN and T80/40/LH supported the growth of L. borgpetersenii serovar Hardjo strain HB15B203 at 29 °C. In addition, HAN supported primary isolation at 37 °C. Both T80/40/LH and HAN supported primary isolation of strain IC:20:001 in liquid media at 29 °C but only HAN supported growth of strain HB15B203 in liquid media, at both 29 and 37 °C. HAN media supports the primary isolation of fastidious pathogenic leptospires directly from infected host tissue at either 29 or 37 °C: this formulation represents a more defined media for the continued optimization of growth factors required to support the primary isolation of the large and diverse range of species and serovars within the genus Leptospira circulating within domestic and wild animal populations. Nature Publishing Group UK 2020-06-15 /pmc/articles/PMC7296004/ /pubmed/32541841 http://dx.doi.org/10.1038/s41598-020-66526-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hornsby, Richard L. Alt, David P. Nally, Jarlath E. Isolation and propagation of leptospires at 37 °C directly from the mammalian host |
title | Isolation and propagation of leptospires at 37 °C directly from the mammalian host |
title_full | Isolation and propagation of leptospires at 37 °C directly from the mammalian host |
title_fullStr | Isolation and propagation of leptospires at 37 °C directly from the mammalian host |
title_full_unstemmed | Isolation and propagation of leptospires at 37 °C directly from the mammalian host |
title_short | Isolation and propagation of leptospires at 37 °C directly from the mammalian host |
title_sort | isolation and propagation of leptospires at 37 °c directly from the mammalian host |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296004/ https://www.ncbi.nlm.nih.gov/pubmed/32541841 http://dx.doi.org/10.1038/s41598-020-66526-4 |
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