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Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization

We conducted a study to determine the main traits of pertussis among unimmunized infants less than 6 months of age. From August 2012 to March 2015, 141 nasopharyngeal aspirates (NPAs) were collected from infants with respiratory symptoms attending 2 major hospitals in Rome. Clinical data were record...

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Autores principales: Stefanelli, Paola, Buttinelli, Gabriele, Vacca, Paola, Tozzi, Alberto E., Midulla, Fabio, Carsetti, Rita, Fedele, Giorgio, Villani, Alberto, Concato, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443365/
https://www.ncbi.nlm.nih.gov/pubmed/28129036
http://dx.doi.org/10.1080/21645515.2016.1276139
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author Stefanelli, Paola
Buttinelli, Gabriele
Vacca, Paola
Tozzi, Alberto E.
Midulla, Fabio
Carsetti, Rita
Fedele, Giorgio
Villani, Alberto
Concato, Carlo
author_facet Stefanelli, Paola
Buttinelli, Gabriele
Vacca, Paola
Tozzi, Alberto E.
Midulla, Fabio
Carsetti, Rita
Fedele, Giorgio
Villani, Alberto
Concato, Carlo
author_sort Stefanelli, Paola
collection PubMed
description We conducted a study to determine the main traits of pertussis among unimmunized infants less than 6 months of age. From August 2012 to March 2015, 141 nasopharyngeal aspirates (NPAs) were collected from infants with respiratory symptoms attending 2 major hospitals in Rome. Clinical data were recorded and analyzed. Lab-confirmation was performed by culture and realtime PCR. B. pertussis virulence-associated genes (ptxP, ptxA and prn), together with multilocus variable-number tandem repeat analysis (MLVA), were also investigated by the sequence-based analysis on the DNAs extracted from positive samples. Antibiotic susceptibility with Etest was defined on 18 viable B. pertussis isolates. Samples from 73 infants resulted positives for B. pertussis. The median age of the patients was 45 d (range 7–165); 21 infants were treated with macrolides before hospital admission. Cough was reported for a median of 10 d before admission and 18 d after hospital discharge among infected infants, 84% of whom showed paroxysmal cough. No resistance to macrolides was detected. Molecular analysis identified MT27 as the predominant MLVA profile, combined with ptxP3-ptxA1-prn2 associated virulence genes. Although our data may not be generalized to the whole country, they provide evidence of disease severity among infants not vaccinated against pertussis. Moreover, genetically related B. pertussis strains, comprising allelic variants of virulence associated genes, were identified.
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spelling pubmed-54433652017-06-02 Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization Stefanelli, Paola Buttinelli, Gabriele Vacca, Paola Tozzi, Alberto E. Midulla, Fabio Carsetti, Rita Fedele, Giorgio Villani, Alberto Concato, Carlo Hum Vaccin Immunother Research Papers We conducted a study to determine the main traits of pertussis among unimmunized infants less than 6 months of age. From August 2012 to March 2015, 141 nasopharyngeal aspirates (NPAs) were collected from infants with respiratory symptoms attending 2 major hospitals in Rome. Clinical data were recorded and analyzed. Lab-confirmation was performed by culture and realtime PCR. B. pertussis virulence-associated genes (ptxP, ptxA and prn), together with multilocus variable-number tandem repeat analysis (MLVA), were also investigated by the sequence-based analysis on the DNAs extracted from positive samples. Antibiotic susceptibility with Etest was defined on 18 viable B. pertussis isolates. Samples from 73 infants resulted positives for B. pertussis. The median age of the patients was 45 d (range 7–165); 21 infants were treated with macrolides before hospital admission. Cough was reported for a median of 10 d before admission and 18 d after hospital discharge among infected infants, 84% of whom showed paroxysmal cough. No resistance to macrolides was detected. Molecular analysis identified MT27 as the predominant MLVA profile, combined with ptxP3-ptxA1-prn2 associated virulence genes. Although our data may not be generalized to the whole country, they provide evidence of disease severity among infants not vaccinated against pertussis. Moreover, genetically related B. pertussis strains, comprising allelic variants of virulence associated genes, were identified. Taylor & Francis 2017-01-27 /pmc/articles/PMC5443365/ /pubmed/28129036 http://dx.doi.org/10.1080/21645515.2016.1276139 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Papers
Stefanelli, Paola
Buttinelli, Gabriele
Vacca, Paola
Tozzi, Alberto E.
Midulla, Fabio
Carsetti, Rita
Fedele, Giorgio
Villani, Alberto
Concato, Carlo
Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization
title Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization
title_full Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization
title_fullStr Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization
title_full_unstemmed Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization
title_short Severe pertussis infection in infants less than 6 months of age: Clinical manifestations and molecular characterization
title_sort severe pertussis infection in infants less than 6 months of age: clinical manifestations and molecular characterization
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443365/
https://www.ncbi.nlm.nih.gov/pubmed/28129036
http://dx.doi.org/10.1080/21645515.2016.1276139
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