Background: Due to extensive damage to the skin, burn victims may acquire life-threatening infections. Though the skin primarily protects against microbial invasions, a large number of bacteria, fungi, and viruses can be isolated from burn patients, specifically Pseudomonas aeruginosa, a gram-negative bacterium with both intrinsic and acquired antibiotic resistance (AR) properties. nalB mutations can be found on the mexR in the P. aeruginosa chromosome. This mutation can induce overexpression of the mexAB-oprMoperon, and affect the MexAB-OprM efflux pump, which removes antimicrobial agents from the bacterial cell. Identifying nalB mutants can be useful for monitoring factors affecting AR. Methods: In this study, 70 P. aeruginosa isolates identified from burn patients and antibacterial sensitivity was evaluated using the Kirby-Bauer method. We also investigated nalB mutations in samples using molecular methods including Polymerase reaction chain (PCR) and Sequencing. Results: We identified nalB mutations in 16 isolates. We also found that the increasing effect of nalB mutants induces hyper production activity of MexAB-OprM resulting in AR. Overall, these findings compliment the findings of previous reports. Conclusions: According to the resistance patterns of the samples, both Amikacin and Ciprofloxacin showed the highest resistance (%). Further, the relationship between Ciprofloxacin resistance and nalB mutations was statistically significant (p= 0.016). The results confirm that the increasing effect of nalB mutants on hyper production activity of MexAB-OprM leads to AR.
Objective:
Haemophilus influenzae is the causative agent of invasive and noninvasive infections such as chronic obstructive lung disease exacerbation, sinusitis, otitis media, and conjunctivitis. The study was undertaken to direct detection, capsular typing, and investigate the occurrence of β-lactamase resistance genes in H. influenzae strains isolated from sinusitis samples.
Materials and methods:
We investigated the presence of H influenzae in 137 sinusitis samples obtained from the patients had referred to Rasoole-Akram Hospital in Tehran in 2017. DNA extraction was performed according to the QIAamp kit. polymerase chain reaction (PCR) amplification was performed with specific primers to determine H. influenzae and capsular-typing and to detect resistance genes.
Results:
Eleven samples were positive for the presence of H. influenzae. Overall, 5, 2, and 4 isolates were H. influenzae type b, type A, and nontypeable H. influenzae, respectively. Of 11 isolates of H. influenzae, only two isolates (18%) were β-lactamase positive and carried the TEM-1 gene, but others were negative for the ROB-1 gene. As well, the current study showed that 45.5% (n; five of 11 encapsulated H. influenzae) of isolates were type b, which were the predominant types.
Conclusion:
Our data suggest that the conventional PCR can help increase detection rates of bacterial cause of sinusitis and resistance genes in clinical samples for effective treatment in individual sensitive to invasive infection.
Background: One of the causes of male infertility is Genital tract infections (GTI). Considering the importance of GTI, widespread recognition of them seems necessary. we aimed to characterize and compare semen microbial populations in fertile and infertile men who referred to an infertility clinic in Yazd, Iran. Methods: Semen samples were collected from two groups of fertile (268) and infertile (210) men. Sperm analysis (concentration, morphology, viability and motility parameters) were performed according to the World Health Organization (WHO) 2010 guidelines laboratory manual. Bacterial isolation was performed in Sheep Blood Agar and Eosin Methylene Blue (EMB) agar plates. For PCR, samples were analyzed with genus specific primers. Results: All semen characteristics were poor in the infertile group compared to those in the fertile men (p-value< 0.05). Enterococcus spp. (18.7%, 17.1%; p= 0.814), E. coli (7.9%, 11.4%; p= 0.486), Staphylococcus aureus (6.4%, 2.9%; p= 0.398) and Proteus mirabilis (0%, 2.9%; p= 0.002) were the most common agents, respectively. Also, the results obtained from PCR were confirmed using culture-base method. Conclusions: Proteus mirabilis contamination was identified in the infertile group. While no significant association was observed between male infertility and semen microbial populations, p. mirabilis may be the leading cause of reproduction impairment in men.
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