Molecular characterization of the pilS2 gene and its association with the frequency of Pseudomonas aeruginosa plasmid pKLC102 and PAPI-1 pathogenicity island

被引:22
作者
Bahramian, Aghil [1 ,2 ]
Khoshnood, Saeed [3 ,4 ]
Shariati, Aref [5 ]
Doustdar, Farahnoosh [2 ]
Chirani, Alireza Salimi [2 ]
Heidary, Mohsen [5 ,6 ]
机构
[1] Shahid Beheshti Univ Med Sci, Infect Dis & Trop Med Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Fac Med, Dept Microbiol, Golestan St,POB 159, Ahvaz 6135715794, Khuzestan, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Student Res Comm, Ahvaz, Iran
[5] Iran Univ Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
[6] Iran Univ Med Sci, Sch Allied Med Sci, Student Res Comm, Tehran, Iran
来源
INFECTION AND DRUG RESISTANCE | 2019年 / 12卷
关键词
Pseudomonas aeruginosa; pilS2; cystic fibrosis; pKLC102; PAPI-1; PREVALENCE; VIRULENCE; SEQUENCE;
D O I
10.2147/IDR.S188527
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Pseudomonas aeruginosa is the most common opportunistic pathogen associated with a broad range of infections, including cystic fibrosis, ocular, otitis media, and burn infections. The aim of this study was to show the frequency of the pilS2 gene, and its association with P. aeruginosa plasmid pKLC102 and PAPI-1 pathogenicity island among P. aeruginosa strains. Methods: The samples were collected from patients with cystic fibrosis, ocular, otitis media, and burn infections between January 2016 and November 2017. DNA was extracted using the DNA extraction kit and was used for PCR assay. PCR with 4 primer-pairs including 976 F/PAPI-1R, 4542 F/intF, SojR/4541 F, and intF/sojR was performed to identify PAPI-1. pKLC102 was detected using three other primer-pairs including cp10F/cp10R, cp44F/cp44R, and cp97F/cp97R. Results: A total of 112 P. aeruginosa isolates were collected from patients with cystic fibrosis (36), burn (20), otitis media (26), and ocular (30) infections. The results of PCR showed that pilS2 gene was identified in 96 (85%) strains. PAPI-1-attB integration was detected among 38 (33.9%) isolates and the circular form of PAPI-1 detected among 17 (14%) isolates. In addition, 79 (70.5%) strains were found to be positive for pKLC102. Conclusion: We found that the majority of the isolates may be susceptible to transfer this significant island and the related element pKLC102 into recipient isolates lacking the island owing to high association of the PilS2 pilus with the islands in the studied strains. It is anticipated that strains isolated from burn and eye with the highest rate of PilS2, PAPI-1, and pKLC102 association have a high level of antibiotic resistance.
引用
收藏
页码:221 / 227
页数:7
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