2015
DOI: 10.5812/jjm.8(5)2015.18190
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Isolation of High Level Macrolide Resistant Bordetella Pertussis Without Transition Mutation at Domain V in Iran

Abstract: Background:Bordetella pertussis, as a causative agent of whooping cough, due to the annual rise y of infection cases, failure of prophylaxis and treatment by macrolides, is considered as the new concern in the health care system.Objectives:The main objective of this study was the determination of single nucleotide polymorphisms (SNPs) at domain V, as the main binding site for macrolides, following the identification of high level macrolides resistant B. pertussis.Materials and Methods:Following the identificat… Show more

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Cited by 7 publications
(9 citation statements)
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(27 reference statements)
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“…The possible reason to explain this could be that antigens in the vaccine strain used in Iran are different from the circulating pertussis strains in the community. Interestingly, studies by Shahcheraghi et al show that 48% of B. pertussis strains isolated from Iranian patients had allelic differences in ptxP3, ptxA1, prn2, fim 2-1, fim3-2, and cya2 antigens [25,26]. In conclusion, we believe that the prevalence of the disease in children under one year of age can be due to inadequate or incomplete vaccination in this age group.…”
Section: Discussionmentioning
confidence: 61%
“…The possible reason to explain this could be that antigens in the vaccine strain used in Iran are different from the circulating pertussis strains in the community. Interestingly, studies by Shahcheraghi et al show that 48% of B. pertussis strains isolated from Iranian patients had allelic differences in ptxP3, ptxA1, prn2, fim 2-1, fim3-2, and cya2 antigens [25,26]. In conclusion, we believe that the prevalence of the disease in children under one year of age can be due to inadequate or incomplete vaccination in this age group.…”
Section: Discussionmentioning
confidence: 61%
“…Seven virulence-related genes ( ptxA , ptxC , ptxP , prn , fim2 , fim3 , and tcfA2 ) and the 23S rRNA gene of B. pertussis were amplified and sequenced following procedures published previously ( Yang et al, 2015 ; Mooi et al, 2000 ). The mutation A2047G in domain V of the 23S rRNA gene was responsible for ER ( Bartkus et al, 2003 ; Guillot et al, 2012 ; Mirzaei et al, 2015 ; Xu et al, 2019 ), and genotypes were determined as described previously ( Li et al, 2019 ).…”
Section: Methodsmentioning
confidence: 99%
“…One study collecting 256 isolates from nine European countries between 2012 and 2015 showed that the alleles ptxA1 , ptxP3 , and prn2 account for 100, 95.5, and 96.2%, respectively, whereas 24.9% (66/265) of isolates exhibit prn deficiency ( Barkoff et al, 2018 ). Although the macrolides have been the first-choice antibiotics to treat pertussis for more than 50 years worldwide, a few countries other than China (e.g., the United States, France, and Iran) have reported occasional erythromycin-resistant (ER) strains that do not exhibit epidemic trends ( Bartkus et al, 2003 ; Guillot et al, 2012 ; Mirzaei et al, 2015 ). However, previous studies revealed the unique molecular characteristics and common ER phenotype of circulating B. pertussis strains in China ( Fu et al, 2019 ; Li et al, 2019 ; Xu et al, 2019 ; Zhang et al, 2020 ).…”
Section: Introductionmentioning
confidence: 99%
“…There have only been two reports (Iran and China) where the A2047G SNP has not been the mechanism behind the macrolide resistance in B. pertussis [ 22 , 43 ]. However, these two studies did not perform erm gene or mexAB-oprM operon identification, and the reason for the resistance remains unknown.…”
Section: Mechanisms Behind Macrolide Resistance In B Pertussismentioning
confidence: 99%