Investigation of virulence factors and genes associated with biofilm and protease in Stenotrophomonas maltophilia isolates in Bushehr, Iran.

IF 1.7 Q4 MICROBIOLOGY
Neda Shadvar, Forough Yousefi, Afshin Barazesh, Saeed Tajbakhsh
{"title":"Investigation of virulence factors and genes associated with biofilm and protease in <i>Stenotrophomonas maltophilia</i> isolates in Bushehr, Iran.","authors":"Neda Shadvar, Forough Yousefi, Afshin Barazesh, Saeed Tajbakhsh","doi":"10.18502/ijm.v17i4.19229","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>This study aimed to investigate the virulence factors and genes associated with biofilm and protease in <i>Stenotrophomonas maltophilia</i> in Bushehr, Iran.</p><p><strong>Materials and methods: </strong>Eighty-seven <i>S. maltophilia</i> isolates (67 clinical and 20 environmental isolates) were studied. The isolates were assessed for the production of virulence factors including several enzymes and biofilm. To detect <i>rmlA, rpfF, spgM, smf-1, StmPr1</i> 868 bp, <i>StmPr1</i> 1621 bp, and <i>StmPr2</i> genes, PCR and sequencing were performed.</p><p><strong>Results: </strong>All isolates (100%) produced DNase, hemolysin, protease, lipase, and hyaluronidase. Seventy-eight (89.7%) isolates were gelatinase producers, and 85 (97.7%) isolates were lecithinase producers. All isolates were biofilm producers: 79 (90.8%) isolates produced strong biofilm, 5 (5.7%) isolates produced moderate biofilm, and 3 (3.5%) isolates produced weak biofilm. The frequency of <i>smf-1, rmlA, rpfF,</i> and <i>spgM</i> was 93.1%, 86.2%, 26.4%, and 59.8%, respectively. The frequency of protease genes including <i>StmPr1</i> 868 bp, <i>StmPr1</i> 1621 bp, and <i>StmPr2</i> was 12.6%, 41.4%, and 18.4%, respectively.</p><p><strong>Conclusion: </strong>Our findings revealed a high frequency of isolates that produce DNase, hemolysin, protease, gelatinase, lipase, lecithinase, hyaluronidase, and biofilm. All isolates that harbored <i>spgM</i> or <i>rpfF</i> or both genes were strong biofilm producers. Notably, the presence of isolates that lacked <i>spgM</i> and <i>rpfF</i> genes but produced strong biofilm indicates that in addition to these two genes, other genes or factors may play a role in the production of strong biofilm. Based on this research, <i>S. maltophilia</i> in our area possesses the capability to produce several factors that could play roles in pathogenicity.</p>","PeriodicalId":14633,"journal":{"name":"Iranian Journal of Microbiology","volume":"17 4","pages":"559-568"},"PeriodicalIF":1.7000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12331456/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/ijm.v17i4.19229","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background and objectives: This study aimed to investigate the virulence factors and genes associated with biofilm and protease in Stenotrophomonas maltophilia in Bushehr, Iran.

Materials and methods: Eighty-seven S. maltophilia isolates (67 clinical and 20 environmental isolates) were studied. The isolates were assessed for the production of virulence factors including several enzymes and biofilm. To detect rmlA, rpfF, spgM, smf-1, StmPr1 868 bp, StmPr1 1621 bp, and StmPr2 genes, PCR and sequencing were performed.

Results: All isolates (100%) produced DNase, hemolysin, protease, lipase, and hyaluronidase. Seventy-eight (89.7%) isolates were gelatinase producers, and 85 (97.7%) isolates were lecithinase producers. All isolates were biofilm producers: 79 (90.8%) isolates produced strong biofilm, 5 (5.7%) isolates produced moderate biofilm, and 3 (3.5%) isolates produced weak biofilm. The frequency of smf-1, rmlA, rpfF, and spgM was 93.1%, 86.2%, 26.4%, and 59.8%, respectively. The frequency of protease genes including StmPr1 868 bp, StmPr1 1621 bp, and StmPr2 was 12.6%, 41.4%, and 18.4%, respectively.

Conclusion: Our findings revealed a high frequency of isolates that produce DNase, hemolysin, protease, gelatinase, lipase, lecithinase, hyaluronidase, and biofilm. All isolates that harbored spgM or rpfF or both genes were strong biofilm producers. Notably, the presence of isolates that lacked spgM and rpfF genes but produced strong biofilm indicates that in addition to these two genes, other genes or factors may play a role in the production of strong biofilm. Based on this research, S. maltophilia in our area possesses the capability to produce several factors that could play roles in pathogenicity.

Abstract Image

Abstract Image

伊朗布什尔嗜麦芽寡养单胞菌分离株生物膜和蛋白酶相关毒力因子和基因的研究。
背景与目的:本研究旨在调查伊朗布什尔嗜麦芽窄养单胞菌生物膜和蛋白酶相关的毒力因子和基因。材料与方法:对87株嗜麦芽葡萄球菌(67株临床分离株,20株环境分离株)进行了研究。对分离株的产毒因子进行了评估,包括几种酶和生物膜。为检测rmlA、rpfF、spgM、smf-1、StmPr1 868 bp、StmPr1 1621 bp和StmPr2基因,进行PCR和测序。结果:所有分离株(100%)均产生dna酶、溶血素、蛋白酶、脂肪酶和透明质酸酶。产生明胶酶的菌株78株(89.7%),产生卵磷脂酶的菌株85株(97.7%)。所有分离株均为生物膜产生菌:79株(90.8%)产生强生物膜,5株(5.7%)产生中等生物膜,3株(3.5%)产生弱生物膜。smf-1、rmlA、rpfF和spgM的检出率分别为93.1%、86.2%、26.4%和59.8%。蛋白酶基因StmPr1 868 bp、StmPr1 1621 bp和StmPr2的频率分别为12.6%、41.4%和18.4%。结论:我们的研究结果显示,产生dna酶、溶血酶、蛋白酶、明胶酶、脂肪酶、卵磷脂酶、透明质酸酶和生物膜的分离株频率很高。所有携带spgM或rpfF或两种基因的分离株都是强生物膜生产者。值得注意的是,缺乏spgM和rpfF基因但产生强生物膜的分离株的存在表明,除了这两个基因外,其他基因或因素可能在强生物膜的产生中起作用。本研究表明,本地区嗜麦芽葡萄球菌具有产生多种致病因子的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.40
自引率
7.10%
发文量
96
审稿时长
12 weeks
期刊介绍: The Iranian Journal of Microbiology (IJM) is an international, multi-disciplinary, peer-reviewed journal that provides rapid publication of the most advanced scientific research in the areas of basic and applied research on bacteria and other micro-organisms, including bacteria, viruses, yeasts, fungi, microalgae, and protozoa concerning the development of tools for diagnosis and disease control, epidemiology, antimicrobial agents, clinical microbiology, immunology, Genetics, Genomics and Molecular Biology. Contributions may be in the form of original research papers, review articles, short communications, case reports, technical reports, and letters to the Editor. Research findings must be novel and the original data must be available for review by the Editors, if necessary. Studies that are preliminary, of weak originality or merely descriptive as well as negative results are not appropriate for the journal. Papers considered for publication must be unpublished work (except in an abstract form) that is not under consideration for publication anywhere else, and all co-authors should have agreed to the submission. Manuscripts should be written in English.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信