{"title":"金黄色葡萄球菌分离物中粘附和生物膜相关基因的流行和比较分析:一项网络荟萃分析。","authors":"Aram Sharifi, Peyman Mahmoudi, Keyvan Sobhani, Morahem Ashengroph","doi":"10.1111/1348-0421.13189","DOIUrl":null,"url":null,"abstract":"<p><i>Staphylococcus aureus</i> is a versatile pathogen capable of causing a wide range of infections, from minor skin infections to life-threatening invasive diseases. The pathogenicity of <i>S. aureus</i> is attributed to its ability to produce various virulence factors, including adhesion and biofilm-related proteins. Understanding the prevalence and distribution of these genes among <i>S. aureus</i> isolates from different sources is crucial for devising effective strategies to combat biofilm-associated contamination. In this study, we conducted a comprehensive network meta-analysis to assess the prevalence of adhesion and biofilm-related genes in <i>S. aureus</i> isolates and investigate the impact of the isolate source on their occurrence. A systematic search of multiple databases was performed, and a total of 53 relevant studies were included. The prevalence of adhesion and biofilm-related genes in <i>S. aureus</i> isolates was determined, with the highest prevalence observed for <i>clfB</i> (<i>p</i>-estimate = 85.4, 95% confidence interval [CI] 78–90.6), followed by <i>eno</i> (<i>p</i>-estimate = 81.1, 95% CI 61.7–91.9), and <i>icaD</i> (<i>p</i>-estimate = 77, 95% CI 68.6–83.6). Conversely, <i>bap</i> and <i>bbp</i> genes exhibited the lowest prevalence rates (<i>p</i>-estimate = 6.7 and 18.7, respectively). The network meta-analysis allowed us to examine the pairwise co-study of adhesion and biofilm-related genes in <i>S. aureus</i> isolates. The most frequently co-studied gene pairs were <i>icaA</i>-<i>icaD</i> (30 times) and <i>fnbA</i>-<i>fnbB</i> (25 times). Subgroup analysis showed that the occurrence of <i>icaC</i> and <i>icaB</i> genes was significantly lower in animal isolates compared to human and food isolates (<i>p</i> < 0.05). It is worth noting that there was limited data available for the analysis of <i>sasG</i>, <i>bbp</i>, <i>bap</i>, <i>eno</i>, and <i>fib</i> genes. In conclusion, the study revealed varying prevalence rates of adhesion and biofilm-related genes in <i>S. aureus</i> isolates. Genes such as <i>clfB</i>, <i>eno</i>, and <i>icaD</i> were found to be highly prevalent, while <i>bap</i> and <i>bbp</i> were less common. Limited existing data on the prevalence of genes like <i>sasG</i>, <i>bbp</i>, <i>bap</i>, <i>eno</i>, and <i>fib</i> highlights the need for further research to determine their exact prevalence rates. Our results contribute to a better understanding of <i>S. aureus</i> pathogenesis and can facilitate the development of effective strategies for the prevention and treatment of <i>S. aureus</i> infections.</p>","PeriodicalId":18679,"journal":{"name":"Microbiology and Immunology","volume":"69 2","pages":"104-113"},"PeriodicalIF":1.9000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Prevalence and Comparative Analysis of Adhesion and Biofilm-Related Genes in Staphylococcus aureus Isolates: A Network Meta-Analysis\",\"authors\":\"Aram Sharifi, Peyman Mahmoudi, Keyvan Sobhani, Morahem Ashengroph\",\"doi\":\"10.1111/1348-0421.13189\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Staphylococcus aureus</i> is a versatile pathogen capable of causing a wide range of infections, from minor skin infections to life-threatening invasive diseases. The pathogenicity of <i>S. aureus</i> is attributed to its ability to produce various virulence factors, including adhesion and biofilm-related proteins. Understanding the prevalence and distribution of these genes among <i>S. aureus</i> isolates from different sources is crucial for devising effective strategies to combat biofilm-associated contamination. In this study, we conducted a comprehensive network meta-analysis to assess the prevalence of adhesion and biofilm-related genes in <i>S. aureus</i> isolates and investigate the impact of the isolate source on their occurrence. A systematic search of multiple databases was performed, and a total of 53 relevant studies were included. The prevalence of adhesion and biofilm-related genes in <i>S. aureus</i> isolates was determined, with the highest prevalence observed for <i>clfB</i> (<i>p</i>-estimate = 85.4, 95% confidence interval [CI] 78–90.6), followed by <i>eno</i> (<i>p</i>-estimate = 81.1, 95% CI 61.7–91.9), and <i>icaD</i> (<i>p</i>-estimate = 77, 95% CI 68.6–83.6). Conversely, <i>bap</i> and <i>bbp</i> genes exhibited the lowest prevalence rates (<i>p</i>-estimate = 6.7 and 18.7, respectively). The network meta-analysis allowed us to examine the pairwise co-study of adhesion and biofilm-related genes in <i>S. aureus</i> isolates. The most frequently co-studied gene pairs were <i>icaA</i>-<i>icaD</i> (30 times) and <i>fnbA</i>-<i>fnbB</i> (25 times). Subgroup analysis showed that the occurrence of <i>icaC</i> and <i>icaB</i> genes was significantly lower in animal isolates compared to human and food isolates (<i>p</i> < 0.05). It is worth noting that there was limited data available for the analysis of <i>sasG</i>, <i>bbp</i>, <i>bap</i>, <i>eno</i>, and <i>fib</i> genes. In conclusion, the study revealed varying prevalence rates of adhesion and biofilm-related genes in <i>S. aureus</i> isolates. Genes such as <i>clfB</i>, <i>eno</i>, and <i>icaD</i> were found to be highly prevalent, while <i>bap</i> and <i>bbp</i> were less common. Limited existing data on the prevalence of genes like <i>sasG</i>, <i>bbp</i>, <i>bap</i>, <i>eno</i>, and <i>fib</i> highlights the need for further research to determine their exact prevalence rates. Our results contribute to a better understanding of <i>S. aureus</i> pathogenesis and can facilitate the development of effective strategies for the prevention and treatment of <i>S. aureus</i> infections.</p>\",\"PeriodicalId\":18679,\"journal\":{\"name\":\"Microbiology and Immunology\",\"volume\":\"69 2\",\"pages\":\"104-113\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-12-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbiology and Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/1348-0421.13189\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology and Immunology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1348-0421.13189","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
金黄色葡萄球菌是一种多功能病原体,能够引起广泛的感染,从轻微的皮肤感染到危及生命的侵袭性疾病。金黄色葡萄球菌的致病性归因于其产生各种毒力因子的能力,包括粘附和生物膜相关蛋白。了解这些基因在不同来源的金黄色葡萄球菌分离株中的流行和分布对于制定有效的策略来对抗生物膜相关污染至关重要。在这项研究中,我们进行了一项全面的网络荟萃分析,以评估金黄色葡萄球菌分离株中粘附和生物膜相关基因的患病率,并研究分离源对其发生的影响。系统检索多个数据库,共纳入53项相关研究。测定了金黄色葡萄球菌分离株中粘附和生物膜相关基因的患病率,其中clfB的患病率最高(p-估计= 85.4,95%可信区间[CI] 78-90.6),其次是eno (p-估计= 81.1,95% CI 61.7-91.9)和icaD (p-估计= 77,95% CI 68.6-83.6)。相反,bap和bbp基因的患病率最低(p-estimate分别为6.7和18.7)。网络荟萃分析使我们能够检查金黄色葡萄球菌分离株中粘附和生物膜相关基因的两两共同研究。共同研究次数最多的基因对是icaA-icaD(30次)和fnbA-fnbB(25次)。亚组分析显示,与人类和食物分离株相比,动物分离株中icaC和icaB基因的发生率显著降低
The Prevalence and Comparative Analysis of Adhesion and Biofilm-Related Genes in Staphylococcus aureus Isolates: A Network Meta-Analysis
Staphylococcus aureus is a versatile pathogen capable of causing a wide range of infections, from minor skin infections to life-threatening invasive diseases. The pathogenicity of S. aureus is attributed to its ability to produce various virulence factors, including adhesion and biofilm-related proteins. Understanding the prevalence and distribution of these genes among S. aureus isolates from different sources is crucial for devising effective strategies to combat biofilm-associated contamination. In this study, we conducted a comprehensive network meta-analysis to assess the prevalence of adhesion and biofilm-related genes in S. aureus isolates and investigate the impact of the isolate source on their occurrence. A systematic search of multiple databases was performed, and a total of 53 relevant studies were included. The prevalence of adhesion and biofilm-related genes in S. aureus isolates was determined, with the highest prevalence observed for clfB (p-estimate = 85.4, 95% confidence interval [CI] 78–90.6), followed by eno (p-estimate = 81.1, 95% CI 61.7–91.9), and icaD (p-estimate = 77, 95% CI 68.6–83.6). Conversely, bap and bbp genes exhibited the lowest prevalence rates (p-estimate = 6.7 and 18.7, respectively). The network meta-analysis allowed us to examine the pairwise co-study of adhesion and biofilm-related genes in S. aureus isolates. The most frequently co-studied gene pairs were icaA-icaD (30 times) and fnbA-fnbB (25 times). Subgroup analysis showed that the occurrence of icaC and icaB genes was significantly lower in animal isolates compared to human and food isolates (p < 0.05). It is worth noting that there was limited data available for the analysis of sasG, bbp, bap, eno, and fib genes. In conclusion, the study revealed varying prevalence rates of adhesion and biofilm-related genes in S. aureus isolates. Genes such as clfB, eno, and icaD were found to be highly prevalent, while bap and bbp were less common. Limited existing data on the prevalence of genes like sasG, bbp, bap, eno, and fib highlights the need for further research to determine their exact prevalence rates. Our results contribute to a better understanding of S. aureus pathogenesis and can facilitate the development of effective strategies for the prevention and treatment of S. aureus infections.
期刊介绍:
Microbiology and Immunology is published in association with Japanese Society for Bacteriology, Japanese Society for Virology, and Japanese Society for Host Defense Research. It is peer-reviewed publication that provides insight into the study of microbes and the host immune, biological and physiological responses.
Fields covered by Microbiology and Immunology include:Bacteriology|Virology|Immunology|pathogenic infections in human, animals and plants|pathogenicity and virulence factors such as microbial toxins and cell-surface components|factors involved in host defense, inflammation, development of vaccines|antimicrobial agents and drug resistance of microbes|genomics and proteomics.