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Genomic analysis of the population structure of Paenibacillus larvae in New Zealand
New Zealand is a remote country in the South Pacific Ocean. The isolation and relatively late arrival of humans into New Zealand has meant there is a recorded history of the introduction of domestic species. Honey bees (Apis mellifera) were introduced to New Zealand in 1839, and the disease American...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157257/ https://www.ncbi.nlm.nih.gov/pubmed/37152741 http://dx.doi.org/10.3389/fmicb.2023.1161926 |
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author | Binney, Barbara M. Pragert, Hayley Foxwell, Jonathan Gias, Edna Birrell, Meredith L. Phiri, Bernard J. Quinn, Oliver Taylor, Michael Ha, Hye Jeong Hall, Richard J. |
author_facet | Binney, Barbara M. Pragert, Hayley Foxwell, Jonathan Gias, Edna Birrell, Meredith L. Phiri, Bernard J. Quinn, Oliver Taylor, Michael Ha, Hye Jeong Hall, Richard J. |
author_sort | Binney, Barbara M. |
collection | PubMed |
description | New Zealand is a remote country in the South Pacific Ocean. The isolation and relatively late arrival of humans into New Zealand has meant there is a recorded history of the introduction of domestic species. Honey bees (Apis mellifera) were introduced to New Zealand in 1839, and the disease American foulbrood was subsequently found in the 1870s. Paenibacillus larvae, the causative agent of American foulbrood, has been genome sequenced in other countries. We sequenced the genomes of P. larvae obtained from 164 New Zealand apiaries where American foulbrood was identified in symptomatic hives during visual inspection. Multi-locus sequencing typing (MLST) revealed the dominant sequence type to be ST18, with this clonal cluster accounting for 90.2% of isolates. Only two other sequence types (with variants) were identified, ST5 and ST23. ST23 was only observed in the Otago area, whereas ST5 was limited to two geographically non-contiguous areas. The sequence types are all from the enterobacterial repetitive intergenic consensus I (ERIC I) genogroup. The ST18 and ST5 from New Zealand and international P. larvae all clustered by sequence type. Based on core genome MLST and SNP analysis, localized regional clusters were observed within New Zealand, but some closely related genomes were also geographically dispersed, presumably due to hive movements by beekeepers. |
format | Online Article Text |
id | pubmed-10157257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101572572023-05-05 Genomic analysis of the population structure of Paenibacillus larvae in New Zealand Binney, Barbara M. Pragert, Hayley Foxwell, Jonathan Gias, Edna Birrell, Meredith L. Phiri, Bernard J. Quinn, Oliver Taylor, Michael Ha, Hye Jeong Hall, Richard J. Front Microbiol Microbiology New Zealand is a remote country in the South Pacific Ocean. The isolation and relatively late arrival of humans into New Zealand has meant there is a recorded history of the introduction of domestic species. Honey bees (Apis mellifera) were introduced to New Zealand in 1839, and the disease American foulbrood was subsequently found in the 1870s. Paenibacillus larvae, the causative agent of American foulbrood, has been genome sequenced in other countries. We sequenced the genomes of P. larvae obtained from 164 New Zealand apiaries where American foulbrood was identified in symptomatic hives during visual inspection. Multi-locus sequencing typing (MLST) revealed the dominant sequence type to be ST18, with this clonal cluster accounting for 90.2% of isolates. Only two other sequence types (with variants) were identified, ST5 and ST23. ST23 was only observed in the Otago area, whereas ST5 was limited to two geographically non-contiguous areas. The sequence types are all from the enterobacterial repetitive intergenic consensus I (ERIC I) genogroup. The ST18 and ST5 from New Zealand and international P. larvae all clustered by sequence type. Based on core genome MLST and SNP analysis, localized regional clusters were observed within New Zealand, but some closely related genomes were also geographically dispersed, presumably due to hive movements by beekeepers. Frontiers Media S.A. 2023-04-20 /pmc/articles/PMC10157257/ /pubmed/37152741 http://dx.doi.org/10.3389/fmicb.2023.1161926 Text en Copyright © 2023 Binney, Pragert, Foxwell, Gias, Birrell, Phiri, Quinn, Taylor, Ha and Hall. https://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 Binney, Barbara M. Pragert, Hayley Foxwell, Jonathan Gias, Edna Birrell, Meredith L. Phiri, Bernard J. Quinn, Oliver Taylor, Michael Ha, Hye Jeong Hall, Richard J. Genomic analysis of the population structure of Paenibacillus larvae in New Zealand |
title | Genomic analysis of the population structure of Paenibacillus larvae in New Zealand |
title_full | Genomic analysis of the population structure of Paenibacillus larvae in New Zealand |
title_fullStr | Genomic analysis of the population structure of Paenibacillus larvae in New Zealand |
title_full_unstemmed | Genomic analysis of the population structure of Paenibacillus larvae in New Zealand |
title_short | Genomic analysis of the population structure of Paenibacillus larvae in New Zealand |
title_sort | genomic analysis of the population structure of paenibacillus larvae in new zealand |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157257/ https://www.ncbi.nlm.nih.gov/pubmed/37152741 http://dx.doi.org/10.3389/fmicb.2023.1161926 |
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