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Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene
One of the most important species of the Bartonella genus is B. henselae that causes a zoonotic infection, cat scratch disease (CSD). The main source of the bacteria is cat and the carrier is Ctenocephalides felis flea. One hundred and forty nail and saliva samples were collected from 70 domestic ca...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Urmia University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867040/ https://www.ncbi.nlm.nih.gov/pubmed/27226890 |
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author | Mazaheri Nezhad Fard, Ramin Vahedi, Seyed Milad Ashrafi, Iraj Alipour, Faranak Sharafi, Golnaz Akbarein, Hesam Aldavood, Seyed Javid |
author_facet | Mazaheri Nezhad Fard, Ramin Vahedi, Seyed Milad Ashrafi, Iraj Alipour, Faranak Sharafi, Golnaz Akbarein, Hesam Aldavood, Seyed Javid |
author_sort | Mazaheri Nezhad Fard, Ramin |
collection | PubMed |
description | One of the most important species of the Bartonella genus is B. henselae that causes a zoonotic infection, cat scratch disease (CSD). The main source of the bacteria is cat and the carrier is Ctenocephalides felis flea. One hundred and forty nail and saliva samples were collected from 70 domestic cats. Positive samples for B. henselae were characterized by polymerase chain reaction (PCR) and sequencing. Sequences of gltA gene were trimmed using BioEdit software and then compared with the sequences of the same gene from B. henselae isolated from cats and humans in GenBank database. Phylogenic tree was constructed using CLC Sequence Viewer software and unweighted pair group method with arithmetic mean (UPGMA) method. Molecular assessments showed that five samples out of 70 nail samples (7.14%) and one sample out of 70 saliva samples (1.42%) were genetically positive for B. henselae. At least an 87.00% similarity was seen between the gene sequences from the current study and the reference sequences from the GenBank database. Phylogenic analysis has shown that strains isolated in this study were grouped in a different haplo group, compared to other strains. Among the Asian countries, the prevalence of the bacteria in Iran was close to that in Japan and Turkey. In conclusion, findings of this study showed the prevalence of B. henselae in Iranian cats which is important due to its public health issues, especially for the immunocompromised pet owners. |
format | Online Article Text |
id | pubmed-4867040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Urmia University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48670402016-05-25 Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene Mazaheri Nezhad Fard, Ramin Vahedi, Seyed Milad Ashrafi, Iraj Alipour, Faranak Sharafi, Golnaz Akbarein, Hesam Aldavood, Seyed Javid Vet Res Forum Short Communication One of the most important species of the Bartonella genus is B. henselae that causes a zoonotic infection, cat scratch disease (CSD). The main source of the bacteria is cat and the carrier is Ctenocephalides felis flea. One hundred and forty nail and saliva samples were collected from 70 domestic cats. Positive samples for B. henselae were characterized by polymerase chain reaction (PCR) and sequencing. Sequences of gltA gene were trimmed using BioEdit software and then compared with the sequences of the same gene from B. henselae isolated from cats and humans in GenBank database. Phylogenic tree was constructed using CLC Sequence Viewer software and unweighted pair group method with arithmetic mean (UPGMA) method. Molecular assessments showed that five samples out of 70 nail samples (7.14%) and one sample out of 70 saliva samples (1.42%) were genetically positive for B. henselae. At least an 87.00% similarity was seen between the gene sequences from the current study and the reference sequences from the GenBank database. Phylogenic analysis has shown that strains isolated in this study were grouped in a different haplo group, compared to other strains. Among the Asian countries, the prevalence of the bacteria in Iran was close to that in Japan and Turkey. In conclusion, findings of this study showed the prevalence of B. henselae in Iranian cats which is important due to its public health issues, especially for the immunocompromised pet owners. Urmia University Press 2016 2016-03-15 /pmc/articles/PMC4867040/ /pubmed/27226890 Text en © 2016 Urmia University. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Mazaheri Nezhad Fard, Ramin Vahedi, Seyed Milad Ashrafi, Iraj Alipour, Faranak Sharafi, Golnaz Akbarein, Hesam Aldavood, Seyed Javid Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene |
title | Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene |
title_full | Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene |
title_fullStr | Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene |
title_full_unstemmed | Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene |
title_short | Molecular identification and phylogenic analysis of Bartonella henselae isolated from Iranian cats based on gltA gene |
title_sort | molecular identification and phylogenic analysis of bartonella henselae isolated from iranian cats based on glta gene |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867040/ https://www.ncbi.nlm.nih.gov/pubmed/27226890 |
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