Study the Role of Ph in Curli Biogenesis Gene Expression in Enterobacter Cloacae Local Isolates

Enterobacter cloacae is the most common pathogenic species of the genus Enterobacter, identified inhospitalized and enfeebled patients as the etiologic agent of many infections and considered as a significantbacterial pathogen in recent years. E. Cloacae are typical gram negative opportunistic forms of bacteria thatcause illness after another infection or injury has influenced the host immune system and are related withnosocomial infections. The infection may be caused by GIT, UTI or cross contamination of the blood. Thepresent study focused on the existence of the main curli biogenesis gene (csgA) and the role of pH as anenvironmental factor in the gene expression (csgA) for curli biogenesis. In this study, urine samples from75 patients.In Baghdad city clinically diagnosed with urinary tract infection,for gram staining, Api20Systemand gene expression (csgA) gene in Standardized pH7 and acid pH4 RT-PCR was performed with specificprimers. Conventional gram staining techniques, agricultural methods and System API 20E showed goodresults for E. Cloacae. For the 75 patients, 10 (13.3%) the findings find the highest gene expression foldvalues for the (csgA)gene in pH7 while the lowest fold value for (csgA) at acid pH4 (0.1577) thus themodify conditions growth such as pH of bacteria E. Cloacae triggers gene expression changes for biogenesisprocess. the findings of rpoB gene expression, which was used as a control gene, indicated that this gene wasgood as a housekeeping gene.

[1]  Maarib N. Rasheed,et al.  Isolation, molecular identification and influence of incubation period on hemolysine gene expression in Serratia marcescens local isolates , 2019 .

[2]  T. A. Ahmed Molecular Investigation of Curli Fimbriae Genes in Enterobacter cloacae Isolated from Various Clinical Sources in Baghdad, Iraq , 2018 .

[3]  S. H. Mohaisen,et al.  STUDY OF SOME ENVIRONMENTAL FACTORS ROLE IN HEMOLYSIN GENE EXPRESSION IN SERRATIA MARCESCENS LOCAL ISOLATES , 2017 .

[4]  Saife D. Al-Ahmer,et al.  Molecular Prevalence of E . coli and Enterobacter cloacae Caused Urinary Tract Infections in Iraqi Patients , 2017 .

[5]  Michael Frankfurter,et al.  Basic Laboratory Procedures In Clinical Bacteriology , 2016 .

[6]  M. Behmanesh,et al.  Detection of Curli Biogenesis Genes Among Enterobacter cloacae Isolated From Blood Cultures , 2015 .

[7]  D. Otzen,et al.  Curli Functional Amyloid Systems Are Phylogenetically Widespread and Display Large Diversity in Operon and Protein Structure , 2012, PloS one.

[8]  Jungmin Kim,et al.  Involvement of curli fimbriae in the biofilm formation of Enterobacter cloacae , 2012, The Journal of Microbiology.

[9]  M. Zarkesh,et al.  Entrobacter, the Most Common Pathogen of Neonatal Septicemia in Rasht, Iran , 2011, Iranian journal of pediatrics.

[10]  M. Motlagh,et al.  THE PREVALENCE OF BACTERIA ISOLATED FROM BLOOD CULTURES OF IRANIAN CHILDREN AND STUDY OF THEIR ANTIMICROBIAL SUSCEPTIBILITIES , 2007 .

[11]  Matthew R Chapman,et al.  Curli biogenesis and function. , 2006, Annual review of microbiology.

[12]  C. van Delden,et al.  Analysis of antibiotic resistance gene expression in Pseudomonas aeruginosa by quantitative real-time-PCR. , 2006, FEMS microbiology letters.

[13]  S. Normark,et al.  Expression of and cytokine activation by Escherichia coli curli fibers in human sepsis. , 2000, The Journal of infectious diseases.