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SNR analysis: molecular investigation of an anthrax epidemic

BACKGROUND: In Italy, anthrax is endemic but occurs sporadically. During the summer of 2004, in the Pollino National Park, Basilicata, Southern Italy, an anthrax epidemic consisting of 41 outbreaks occurred; it claimed the lives of 124 animals belonging to different mammal species. This study is a r...

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Autores principales: Garofolo, Giuliano, Ciammaruconi, Andrea, Fasanella, Antonio, Scasciamacchia, Silvia, Adone, Rosanna, Pittiglio, Valentina, Lista, Florigio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837646/
https://www.ncbi.nlm.nih.gov/pubmed/20187980
http://dx.doi.org/10.1186/1746-6148-6-11
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author Garofolo, Giuliano
Ciammaruconi, Andrea
Fasanella, Antonio
Scasciamacchia, Silvia
Adone, Rosanna
Pittiglio, Valentina
Lista, Florigio
author_facet Garofolo, Giuliano
Ciammaruconi, Andrea
Fasanella, Antonio
Scasciamacchia, Silvia
Adone, Rosanna
Pittiglio, Valentina
Lista, Florigio
author_sort Garofolo, Giuliano
collection PubMed
description BACKGROUND: In Italy, anthrax is endemic but occurs sporadically. During the summer of 2004, in the Pollino National Park, Basilicata, Southern Italy, an anthrax epidemic consisting of 41 outbreaks occurred; it claimed the lives of 124 animals belonging to different mammal species. This study is a retrospective molecular epidemiological investigation carried out on 53 isolates collected during the epidemic. A 25-loci Multiple Locus VNTR Analysis (MLVA) MLVA was initially performed to define genetic relationships, followed by an investigation of genetic diversity between epidemic strains through Single Nucleotide Repeat (SNR) analysis. RESULTS: 53 Bacillus anthracis strains were isolated. The 25-loci MLVA analysis identified all of them as belonging to a single genotype, while the SNR analysis was able to detect the existence of five subgenotypes (SGTs), allowing a detailed epidemic investigation. SGT-1 was the most frequent (46/53); SGTs 2 (4/53), 3 (1/53) 4 (1/53) and 5 (1/53) were detected in the remaining seven isolates. CONCLUSIONS: The analysis revealed the prevalent spread, during this epidemic, of a single anthrax clone. SGT-1 - widely distributed across the epidemic area and present throughout the period in question - may, thus, be the ancestral form. SGTs 2, 3 and 4 differed from SGT-1 at only one locus, suggesting that they could have evolved directly from the latter during the course of this epidemic. SGT-5 differed from the other SGTs at 2-3 loci. This isolate, thus, appears to be more distantly related to SGT-1 and may not be a direct descendant of the lineage responsible for the majority of cases in this epidemic. These data confirm the importance of molecular typing and subtyping methods for in-depth epidemiological analyses of anthrax epidemics.
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spelling pubmed-28376462010-03-13 SNR analysis: molecular investigation of an anthrax epidemic Garofolo, Giuliano Ciammaruconi, Andrea Fasanella, Antonio Scasciamacchia, Silvia Adone, Rosanna Pittiglio, Valentina Lista, Florigio BMC Vet Res Research article BACKGROUND: In Italy, anthrax is endemic but occurs sporadically. During the summer of 2004, in the Pollino National Park, Basilicata, Southern Italy, an anthrax epidemic consisting of 41 outbreaks occurred; it claimed the lives of 124 animals belonging to different mammal species. This study is a retrospective molecular epidemiological investigation carried out on 53 isolates collected during the epidemic. A 25-loci Multiple Locus VNTR Analysis (MLVA) MLVA was initially performed to define genetic relationships, followed by an investigation of genetic diversity between epidemic strains through Single Nucleotide Repeat (SNR) analysis. RESULTS: 53 Bacillus anthracis strains were isolated. The 25-loci MLVA analysis identified all of them as belonging to a single genotype, while the SNR analysis was able to detect the existence of five subgenotypes (SGTs), allowing a detailed epidemic investigation. SGT-1 was the most frequent (46/53); SGTs 2 (4/53), 3 (1/53) 4 (1/53) and 5 (1/53) were detected in the remaining seven isolates. CONCLUSIONS: The analysis revealed the prevalent spread, during this epidemic, of a single anthrax clone. SGT-1 - widely distributed across the epidemic area and present throughout the period in question - may, thus, be the ancestral form. SGTs 2, 3 and 4 differed from SGT-1 at only one locus, suggesting that they could have evolved directly from the latter during the course of this epidemic. SGT-5 differed from the other SGTs at 2-3 loci. This isolate, thus, appears to be more distantly related to SGT-1 and may not be a direct descendant of the lineage responsible for the majority of cases in this epidemic. These data confirm the importance of molecular typing and subtyping methods for in-depth epidemiological analyses of anthrax epidemics. BioMed Central 2010-02-28 /pmc/articles/PMC2837646/ /pubmed/20187980 http://dx.doi.org/10.1186/1746-6148-6-11 Text en Copyright ©2010 Garofolo et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Garofolo, Giuliano
Ciammaruconi, Andrea
Fasanella, Antonio
Scasciamacchia, Silvia
Adone, Rosanna
Pittiglio, Valentina
Lista, Florigio
SNR analysis: molecular investigation of an anthrax epidemic
title SNR analysis: molecular investigation of an anthrax epidemic
title_full SNR analysis: molecular investigation of an anthrax epidemic
title_fullStr SNR analysis: molecular investigation of an anthrax epidemic
title_full_unstemmed SNR analysis: molecular investigation of an anthrax epidemic
title_short SNR analysis: molecular investigation of an anthrax epidemic
title_sort snr analysis: molecular investigation of an anthrax epidemic
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837646/
https://www.ncbi.nlm.nih.gov/pubmed/20187980
http://dx.doi.org/10.1186/1746-6148-6-11
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