جستجوی مقالات مرتبط با کلیدواژه "susceptibility" در نشریات گروه "پزشکی"
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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in December 2019 in Wuhan (China). It soon became widespread so that the World Health Organization (WHO) declared the outbreak of COVID-19 as a pandemic crisis. This disease has caused significant morbidity and mortality in the world. Clinical studies reported that there is a significant correlation between genders, immunogenetic variants, serum levels of some circulating factors, blood groups, and different races with severity and mortality of COVID-19 patients. Hence, some studies have investigated the role of individual genetic background in the susceptibility and vulnerability to COVID-19 infection. It is proposed that host genetic polymorphisms affect the onset and progression of COVID-19 infection and could dramatically impact the virus life cycle. This paper aims to review the state-of-the-art researches on the roles of genetic variants in host cell membrane proteins and blood circulation factors in the prognosis of patients with COVID-19.
Keywords: COVID-19, SARS-Cov-2, Polymorphism, Prognosis, Host Genetic Factors, Susceptibility -
Background and Objectives
Early diagnosis of candidemia is of vital importance in reducing mortality and morbidity. The main objective of the study was to determine the TTP (Time to Positivity) of different species of Candida causing bloodstream infection and to see whether TTP can help differentiate Candida glabrata which is frequently fluconazole resistant from Fluconazole sensitive Candida.
Materials and MethodsTTP (Time to positivity) and AAT (Appropriate Antifungal therapy) were noted for Blood cultures becoming positive for Candida. Presence of Risk factors for candidemia like prolonged ICU stay, neutropenia, Total Parenteral Nutrition (TPN), use of steroids , broad spectrum antibiotics, use of Central Venous Catheter, Foleys catheter were also analyzed.
ResultsThe most frequent isolates were Candida parapsilosis, Candida tropicalis and Candida albicans. The median TTP for all Candida isolates in our study was 34 hours. The diagnostic sensitivity of TTP for detecting C. glabrata and C. tropicalis in patients with candidemia was 88% and 85% respectively. TTP showed that there was no difference in survival between TTP <24 hrs. and > 24hrs. Initiation of antifungal therapy <24 hours and > 24hrs after onset of candidemia had no association with survival.
ConclusionLonger TTP maybe predictive of C. glabrata while shorter TTP may be predictive of C. tropicalis. In our study we found that fluconazole resistant Candida causing blood stream infection is quite unlikely if the TTP of the isolate is <48hrs.
Keywords: Candida, Fluconazole, Susceptibility, Resistance, Sensitivity -
Background
Phlebotomus papatasi (Diptera: Psychodidae) is the main vector of zoonotic cutaneous leishmaniasis (ZCL) in Iran. The nonstandard use of pesticides against pests, particularly in agriculture, indirectly has caused the de-velopment of resistance and, consequently, the threat of control measures in ZCL endemic areas. Up to 2023, several reports of resistance in Ph. papatasi have been declared in the Old World. The purpose of this study was to measure the lethal time (LT50 and LT90) of Ph. papatasi sand flies in the ZCL endemic center of Esfahan to DDT and deltamethrin insecticides.
MethodsSand flies were collected in Borkhar and were tested using WHO adult mosquito test kit against DDT 4% and deltamethrin 0.0002%. The sand fly’s survival was recorded during exposure time in 225, 450|, 900, 1800, and 3600-seconds’ intervals for DDT and Deltamethrin and they were allowed to recover for 24 hours. Then LT50 and LT90 were analyzed using probit software. Phlebotomus papatasi were identified using morphological keys and other sand flies’ species were excluded from the analysis.
ResultsThe insecticide against female Ph. papatasi revealed hundred percent mortality when exposed to DDT 4% and deltamethrin 0.0002%. The LT50 and LT90 were 19.32 and 22.74 minutes for DDT 4% and 39.92 and 51.33 minutes for deltamethrin 0.0002% respectively.
ConclusionResults of this study revealed that Ph. papatasi is still susceptible to DDT and deltamethrin. This data pro-vides valuable knowledge to implement effective control strategies against ZCL main vector and help to manage insec-ticide resistance in the region.
Keywords: Insecticide, Phlebotomus papatasi, Susceptibility, Iran -
Background and Objectives
Host genetic changes like single nucleotide polymorphisms (SNPs) are one of the main fac- tors influencing susceptibility to viral infectious diseases. This study aimed to investigate the association between the host SNP of Toll-Like Receptor3 (TLR3) and Toll-Like Receptor7 (TLR7) genes involved in the immune system and susceptibil- ity to COVID-19 in a sample of the Iranian population.
Materials and MethodsThis retrospective case-control study evaluated 244 hospitalized COVID-19 patients as the case group and 156 suspected COVID-19 patients with mild signs as the control group. The genomic DNA of patients was gen- otyped for TLR7 (rs179008 and rs179009) and TLR3 (rs3775291 and rs3775296) SNPs using the polymerase chain reac- tion-restriction fragment length polymorphism (PCR-RFLP) method.
ResultsA significant association between rs179008 SNP in the TLR7 gene and the susceptibility of COVID-19 was found between case and control groups. The AT genotype (Heterozygous) of TLR7 rs179008 A>T polymorphism showed a sig- nificant association with a 2.261-fold increased odds of COVID-19 (P=0.003; adjusted OR: 2.261; 99% CI: 1.117-4.575). In addition, a significant association between TC genotype of TLR7 rs179009 T>C polymorphism and increased odds of COVID-19 (P< 0.0001; adjusted OR: 6.818; 99% CI: 3.149-14.134) were determined. The polymorphism frequency of TLR3 rs3775291 and rs3775296 genotypes were not significantly different between the case and control groups (P> 0.004167).
ConclusionSNPs in TLR7 rs179008 and rs179009 genotypes are considered host genetic factors that could be influenced individual susceptibility to COVID-19. The SNPs in TLR3 (rs3775296 and rs3775291) showed no significant association with COVID-19 in Iranian population.
Keywords: TLR3, TLR7, Genetic polymorphism, COVID-19, Susceptibility -
Background
The ABO/Rh blood groups were related to susceptibility to numerous infectious and non-infectious diseases. Here, the association of ABO/Rh groups with susceptibility to COVID-19 and disease severity was investigated in a population from southeast Iran.
Material and MethodsIn this descriptive study, information regarding the clinical characteristics and ABO/Rh blood groups was collected from 524 patients with COVID-19 from March to October, 2020. The data of blood groups from patients were compared with those from 7365 healthy individuals during the same period. Data was analyzed using SPSS.
ResultsNo significant differences were found between COVID-19 patients and the healthy group regarding the proportions of A, B, and O blood groups. However, the proportion of the AB blood group was significantly higher in COVID-19 patients than that in healthy people (11.8% versus 8.2%, P <0.004). When the A group was considered as a reference, the AB blood group was associated to a greater risk of COVID-19 [OR: 1.45 (1.06-1.98), P<0.02]. No association was found between ABO blood groups and COVID-19 severity. The proportion of the Rh-positive blood group was slightly higher in COVID-19 patients than in the other group. The proportion of Rh-negative patients was greater in severe COVID-19 than in mild and moderate forms (P<0.001). In A, AB, and O blood groups, the proportions of Rh-negative patients were greater in severe COVID-19 than those with mild and moderate disease (P=0.05, P<0.05, and P<0.001, respectively).
ConclusionThe AB blood group was associated with greater susceptibility to COVID-19, while Rh-negative status was positively associated with disease severity.
Keywords: COVID-19, SARS-CoV-2, ABO Blood System, Rh System, Susceptibility, Disease Severity -
Background
Many epidemiological studies have explored the relationship between single-nucleotide polymorphism and hepatocellular carcinoma (HCC). However, the results remain controversial. We performed a large-scale meta-analysis to draw a more precise estimation of the aforementioned association.
MethodsStudies on the association between microRNA (MIR) polymorphisms and HCC risk that had been published up to Sep 30, 2021 were identified by searching the PubMed, Cochrane Library, Google Scholar, Web of Science, and Chinese Biomedical Literature electronic databases and the Excerpta Medical Database. The association between MIR polymorphisms and HCC risk was assessed using odds ratios (ORs) and their 95% confidence intervals (CIs).
ResultsOverall, 29 studies, with a total of 9,263 cases and 10,875 controls, were included in our meta-analysis. MicroRNA149 (MIR149) significantly decreased the risk of developing HCC on the overall population (homozygous model CC vs. TT: OR = 0.703, 95% CI = 0.549-0.899, P = 0.005), and microRNA 196 (MIR196) significantly decreased the risk of developing HCC on the overall population (recessive model TT vs. CT+CC: OR = 0.864, 95% CI = 0.751-0.993, P = 0.04) and on Caucasians (OR = 0.613, 95% CI = 0.414-0.907, P = 0.014).
ConclusionThe MIR149 and MIR196 polymorphisms are the protect factors of developing HCC. The conduct of multi-center and multi-region studies with gene-gene, gene-environment should be considered.
Keywords: Hepatocellular carcinoma, MicroRNA, Polymorphism, Susceptibility, Meta-analysis -
Background
As an emerging pandemic disease, COVID-19 encompasses a spectrum of clinical diagnoses, from the common cold to severe respiratory syndrome. Considering the shreds of evidence demonstrating the relationship between human leukocyte antigen (HLA) allele diversity and infectious disease susceptibility, this study was conducted to determine the association of HLA alleles with COVID-19 severity in Iranian subjects.
MethodsIn this case-control study, a total of 200 unrelated individuals (consisting of 100 people with severe COVID-19 and an average age of 55.54 as the case group, and 100 patients with mild COVID-19 with an average age of 48.97 as the control group) were recruited, and HLA typing (Locus A, B, and DR) was performed using the Olerup sequence-specific oligonucleotide (SSO) HLA-typing kit.
ResultsOur results showed that HLA-A*11 and HLA-DRB1*14 alleles were more frequently observed in severe COVID-19 cases, while HLA-B*52 was more common in mild cases, which was in agreement with some previous studies.
ConclusionOur results confirmed the evidence for the association of HLA alleles with COVID-19 outcomes. We found that HLA-A*11 and HLA-DRB1*14 alleles may be susceptibility factors for severe COVID-19, while HLA-B*52 may be a protective factor. These findings provide new insight into the pathogenesis of COVID-19 and help patient management.
Keywords: COVID-19, HLA, Susceptibility -
Background
One of the principal cigarette smokes (CS) mediated diseases is chronic obstructive pulmonary disease (COPD).
MethodsIn the current case-control study, the relationship between the polymorphisms of interleukin-10 (IL-10), transforming growth factor-β1 (TGF-β1) codon 10, TGF-β1 codon 25, interferon-γ (IFN-γ), and tumor necrosis factor-α (TNF-α) in 213 individuals with COPD and susceptibility to the disease, with 100 healthy age and gender-matched people as a control group, was investigated using PCR-ARMS (polymerase chain reaction-amplification refractory mutation system). Moreover, the combination of the polymorphisms of TGF-β1 codon 10.25 regarding this susceptibility was studied in the same condition.
ResultsThere was a significant difference between polymorphism of TGF-β1 codon 10 (+869 T/C), codon 25 (G+915C), and susceptibility to the disease (OR=0.50; (95 %CI=0.24-1.07, p=0.05), ORCC=5.31; (95% CI: 1.22-23.2); p=0.02), thus polymorphism of IL-10 and TGF-β1 increased the risk of susceptibility to COPD but the polymorphisms of TNF-α (G-308A) and IFN-γ ( + 847 T/A) did not show any association.
ConclusionAll in all, it is recommended that the patients carrying the above-said genotypes should be paid proper attention, especially those who are exposed to chemicals at their workplaces, pollution, and cigarette smoke.
Keywords: Chronic Obstructive Pulmonary Disease, Susceptibility, Gene polymorphism -
Background
Leptin is thought to play an important role in Crohn’s disease (CD) pathogenesis and progression. Independent studies have revealed a strong upregulation of leptin expression in the mesenteric fat of CD patients.
ObjectivesThis study assessed the relationship between leptin gene polymorphisms and CD susceptibility in a Chinese pediatric population.
MethodsA total of 86 patients withCDand 142 healthy controls were recruited for this case-control study. The genotypes of 4 singlenucleotide polymorphisms (SNPs; rs2071045, rs41457646, rs11761556, and rs2167270) in the leptin gene were determined by multiplex polymerase chain reaction (PCR) combined with next-generation sequencing.
ResultsWe found that leptin rs2167270 had a significantly different distribution of alleles and genotypes between CD patients and healthy controls (G is a risk allele: 83.7% of cases vs 72.5% of controls; odds ratio [OR] 1.947; 95% CI, 1.203-3.151; P = 0.006; GG is a risk genotype: 72.1% of cases vs 53.5% of controls; P = 0.021). Patients with the CC genotype (rs2071045) had a significantly increased risk of early onset of CD (58.3% in A1a vs 31.1% in A1b; P = 0.003). Similarly, patients carrying the G allele (100% in A1a vs 84.1% in A1b; P = 0.015) and GG genotype (100% in A1a vs 71.0% in A1b; P = 0.048) of rs41457646, A allele (93.3% in A1a vs 71.8% in A1b; P = 0.013) and AA genotype (93.3% in A1a vs 47.9% in A1b; P = 0.003) in rs11761556 had a higher risk of early onset of CD. However, there was no significant difference in any of these 4 SNPs between patients with and without perianal lesions, as well as in low and normal body mass index (BMI) patients.
ConclusionsThe leptin rs2167270 polymorphism is associated with the susceptibility toCDin a Chinese pediatric population. Leptin rs2071045, rs41457646, and rs11761556 might lead to the early onset of pediatric CD.
Keywords: Crohn’s Disease, Polymorphisms, Susceptibility, Leptin -
Background and Objectives
Bacterial causes of gastroenteritis include Salmonella, Shigella spp, diarrheagenic Esche- richia coli, Vibrio cholera and Campylobacter spp. Although infections caused by NTS (Non Typhoidal Salmonella) and Shigella are usually self-limiting, antibiotic treatment is prefered in severely ill or immunocompromised individuals. The main objective of the study was to find out the prevalence of Salmonella and Shigella among the stool samples received in Believers Church Medical College hospital and the antimicrobial susceptibility pattern of Salmonella spp. and Shigella spp.
Materials and MethodsA total of 805 stool samples collected from cases of diarrhea from January 2018 to December 2021 were processed in the laboratory. Standard bacteriological methods were used to isolate, identify, and determine the antimi- crobial susceptibility pattern of Salmonella and Shigella isolates using the disc diffusion method and interpreted according to CLSI.
ResultsA total of 100 (12.4%) samples yielded bacterial pathogens. Salmonella was isolated from 97 (12%) samples and Shigella from 3 (0.4%) samples. Salmonella enterica serovar Typhimurium was the predominant serotype, accounting for 53 (54.6%) isolates.
ConclusionThis study showed Salmonella enterica serovar Typhimurium as the predominant isolate causing diarrheal illness. The emergence of multidrug resistant phenotypes warrants the continuous monitoring of susceptibility trend of NTS in India.
Keywords: Salmonella, Shigella, Susceptibility, Resistance, Diarrhea -
Background
Gujarat State has been witnessing large scale urbanization, in last two decades, resulting changes in local environment and microclimate may have also influenced the resting, feeding habits and development of Anopheles culicifacies sensu 1ato. Therefore, a systematic longitudinal study was undertaken to know the bionomics of An. culicifacies s.l. in present study.
MethodsThe study was conducted in four sentinel villages in Kheda and Panchmahal Districts. The mosquitoes resting indoors and outdoors were collected in early morning hours, using mouth aspirator, pyrethrum space spray and light traps. Mosquito landing collections on human volunteers was carried out from dusk to dawn. Species composition, abundance, seasonal prevalence, resting behavior (Endophily and Exophily), sibling species composition, vector potential and insecticide susceptibility status of malaria vectors was studied.
ResultsSix Anopheles species were collected, An. subpictus s.l. was the predominant species followed by An. culicifacies s.l., a known malaria vector was resting indoor and zoophagic behaviour. Anopheles culicifacies, sibling species B (89%) was found. The sporozoite rate (%) and entomological inoculation rate in Kheda was 2.33%, 3.09 per bite/ person/ annum and they were 1.05% and 0.475 bite/person/annum in Panchmahal, respectively. Anopheles culicifacies s.l. was found possible resistance to alpha-cypermethrin.
ConclusionAnopheles culicifacies s.l. showed endophillic, zoophagic behaviour and found possible resistance to alpha- cypermethrin. Early biting behaviour of An. culicifacies s.l. in this area is a cause of concern. Therefore, there is need for frequent monitoring and evaluation of vector control measures in order to achieve the elimination target of malaria in this area.
Keywords: Endophilic, Zoophagic, Alpha-cypermethrin, Susceptibility, Sibling species -
Background
Among neglected zoonotic diseases, leishmaniases caused by Leishmania parasite through infected female sand fly bite, are a group of diseases found in 98 countries and territories representing a critical burden of disease worldwide. Vector management plays a crucial role in reducing the burden of vector-borne diseases by WHO’s global plan. The objective of the current study was to assess the susceptibility status of wild phlebotomine sand flies from Esfahan Province, central Iran, to the recommended insecticides by WHO.
MethodsSand flies were collected by mouth aspirator in Matin Abad desert Eco-resort and were tested using WHO adult mosquito test kit against Dichlorodiphenyltrichloroethane (DDT) 4%, Deltamethrin 0.05%, Malathion 5% and Propoxur 0.1%. The number of knockdown sand flies were recorded during exposure time in ten minutes interval for DDT and Deltamethrin and they were allowed to recover for 24 hours. Knockdown Time50 (KD50) and KD90 were generated for them using Probit software. They were mounted and identified by valid keys.
ResultsAmong the tested insecticides against female Phlebotomus papatasi, DDT, Deltamethrin, and Malathion recorded the highest mortality rate of 100%, followed by Propoxur with 92.2% mortality for a one-hour exposure. For DDT, KD50 and KD90 were calculated 21.87 and 42.93 and for Deltamethrin, they were 23.74 and 56.50 minutes respectively. Total sand flies exposed with DDT and Deltamethrin shed their leg(s).
ConclusionIt is concluded that Ph. papatasi from central Iran is susceptible to DDT, Deltamethrin, Malathion, and Propoxur.
Keywords: Phlebotomus papatasi, Insecticide, Susceptibility, Iran -
This paper has aimed to review the available evidence on the association between Interleukin (IL) -10 -1082G/A, -592C/A gene polymorphisms and the risk of human immunodeficiency virus-1(HIV-1) infection. The data of PubMed updated in May 2021 were retrieved. The HIV infection risks were estimated in allelic, recessive, dominant, homozygous, heterozygous, over-dominant models of IL-10-1082G/A and-592C/A gene locus as odds ratio (OR) with the corresponding 95% confidence interval (95% CI). The correlation was not significant between -1082G/A polymorphism and HIV-1 susceptibility (allelic model (G vs. A: OR (95% CI)=0.968 (0.878-1.067)); recessive model (GG vs. AA+AG: OR (95% CI)=0.940, (0.771-1.146)); dominant model (GG+AG vs. AA: OR (95% CI)=0.967(0.846-1.106)); homozygous model (GG vs. AA: OR (95% CI)=0.971(0.780-1.209)); heterozygous model (AG vs. AA: OR (95% CI)=0.988(0.797-1.224)) and over-dominant model (GG+AA vs. AG: OR (95% CI)=0.969(0.781-1.201)). IL-10-592C/A polymorphism might be related to HIV-1 in allelic model, dominant model, homozygous model and heterozygous model (OR (95% CI)(0.796-0.965); OR (95% CI)=0.793(0.664-0.948); OR (95% CI)=0.755,(0.612-0.930); OR (95% CI)=0.820(0.679-0.991), respectively), but not to recessive model and over-dominant model (OR (95% CI)=0.882(0.770-1.010) and OR (95% CI)=1.009(0.897-1.148)).
Keywords: HIV-1, Interleukin-10, Meta-analysis, Polymorphism, Susceptibility -
Background
Malaria is a major public health problem in Nigeria with 97% of its population with high morbidity and mortality. Mosquitoes play an important role in the transmission of malaria parasites. This study was conducted to evaluate the current resistance status of Anopheles gambiae to insecticides.
MethodsLarvae of An. gambiae was collected from three zones; A, B and C differentiated on the basis of variation in agricultural ecosystems between August and November, 2018 in the northeast and northwestern parts of Nigeria. They were carefully reared to adult stage and insecticidal susceptibility tests were conducted.
ResultsThe mosquitoes tested showed high levels of resistance to all the insecticides used with the exception of mala thion. Study zone A, recorded 74% mortality after 24h to deltamethrin compared to 81% from zone B and 82% from zone C, respectively. Mosquitoes from zone B exposed to DDT had the highest level of resistance at 37% compared to 40% and 53% from zones A and C, respec tively. Resistant to bendiocarb was also observed, with zone A having the lowest mortality of 44% com pared to 48% from zone C and 55% from Zone B, respectively. According to the results of knockdown tests, mosquitoes from Zone A exposed to deltamethrin recorded the lowest knockdown across the study locations while zone B recorded the lowest knockdown for DDT.
ConclusionThe results of the study provide an insight into the current status of An. gambiae to four major insecticides in northern Nigeria as guideline for mosquitocontrol.
Keywords: Malaria, Anopheles gambiae, Insecticide resistance, Susceptibility, Northern Nigeria -
Objective(s)
The mitogen-activated protein kinase kinase 4 (MKK4) plays a key role in several processes like inflammation, apoptosis, and tumorigenesis. Several authors have proposed that genetic variations in these genes may alter their expression with subsequent cancer risk. This study aimed to examine the possible association of MKK4 rs3826392 and rs3809728 variants in Mexican patients with colorectal cancer (CRC). These variants were also compared with clinical features as sex, age, TNM stage, and tumor location.
Materials and MethodsThe study included genomic DNA from 218 control subjects and 250 patients. Genotyping of the MKK4 variants was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) procedure.
ResultsIndividuals with A/T and T/T genotypes for the rs3809728 (-1044 A>T) variant showed a significantly increased risk for CRC (P=0.012 and 0.007, respectively); while individuals with the G/G genotype for the rs3826392 (-1304 T>G) variant showed a decreased risk for CRC (P=0.012). Genotypes of the MKK4 rs3809728 variant were also significantly related to colon localization and advanced TNM stage in CRC patients. T-T haplotype (rs3826392 and rs3809728) of the MKK4 gene was associated with risk in patients with CRC.
ConclusionThe rs3826392 variant in the MKK4 gene could be a cancer protective factor, while the rs3809728 variant could be a risk factor. These variants play a significant role in CRC risk.
Keywords: Colorectal cancer, Haplotypes, MKK4, Susceptibility, Variants -
Background
Collecting live sand flies from indoor sites is a major challenge for researchers in large cities due to the reluctance of families to survey their homes. This study was conducted to assess the efficacy of two methods for col lecting sand flies for use in susceptibility tests in the urban area of Kerman, southeastern Iran.
MethodsSandflies were mainly collected using both baited traps and hand catch methods from outdoor and indoor sites. Susceptibility tests were separately done according to the standard World Health Organization testing protocol on Phlebotomus sergenti, including 60-minute exposure to DDT 4.0%, propoxur 0.1%, deltamethrin 0.05%, and malathion 5.0%.
ResultsDuring this research, the natural habitats and suitable indoor sites were selected to predict the density of live sand fly with perfect accuracy. The number of live Ph. sergenti caught by hand catch and baited traps methods was 42 and 361 in indoor and outdoor sites, respectively. The mortality rate of Ph. sergenti exposed to DDT 4%, deltamethrin 0.05, malathion 5%, and propoxur was 100%.
ConclusionThe baited traps showed a significant efficiency compared to hand catch for collecting live Ph. sergenti for use in susceptibility tests in urban areas. The Ph. sergenti collected from both indoor and outdoor sites were suscep tible to all insecticides.
Keywords: Phlebotomus sergenti, Susceptibility, Insecticides, Baited traps, Hand catch -
Purpose
To explore the association between MEG3 polymorphisms and the risk of prostate cancer in the Chinese Han population.
Materials and MethodsTwo MEG3 single-nucleotide polymorphisms (SNPs) (rs11627993 C >T rs7158663 A>G) were genotyped in a case-control study in which 165 prostate cancer patients and 200 healthy controls were recruited by a Real-Time Polymerase Chain Reaction (PCR) with the TaqMan assay. The odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the strength of association.
ResultsNo statistically significant differences were found in the allele or genotype distributions of the MEG3 rs11627993 C >T and rs7158663 A > G polymorphisms among cases or healthy control subjects (rs11627993: CC vs CA: 95% CI = 0.54-1.95, ORs = 1.03; CC vs AA: 95% CI = 0.67-2.54, ORs = 1.30 ; CC/CA vs AA: 95% CI = 0.81-1.98, ORs = 1.26 , P = .29 ; C vs A: 95% CI = 0.85-1.57, ORs = 1.16, P = .35; rs7158663: AA vs AG: 95% CI = 0.76-5.08, ORs = 1.97, AA vs GG: 95% CI = 0.57-3.29, ORs = 1.37; AA/AG vs GG : 95% CI = 0.56-1.32, ORs = 0.86, P = .49; A vs G: 95% CI = 0.69-1.39, ORs = 0.98, P = .91) Further stratified analysis detected no significant association.
ConclusionThe MEG3 polymorphisms (rs11627993 C>T and rs7158663 A>G) does not influence the suscepti-bility to prostate cancer.
Keywords: maternal-expressed gene 3, polymorphism, susceptibility, prostate cancer, lncRNA -
Background and Objectives
Bacterial antibiotic resistance is one of the most important threats for public health around the world. Carbapenemase-producing Gram-negative bacteria have resistance to most antibiotics including carbapenems complicating the treatment of infections. The aim of this study was to determine the antimicrobial susceptibility pattern of carbapenemase-producing nosocomial Gram-negative pathogens at a referral teaching hospital to reveal the best options for treatment of related infections.
Materials and MethodsGram-negative bacteria, isolated from hospitalized patients with nosocomial infections, underwent meropenem susceptibility test by disk diffusion method. Meropenem-resistant strains were evaluated for the presence of carbapenemase using Modified Hodge test (MHT). Finally, the antibiotic susceptibility test was performed to determine the sensitivity of each carbapenemase-positive strain against various antimicrobial agents according to the guidelines of Clinical and Laboratory Standards Institute (CLSI).
ResultsOver the study period, 155 carbapenemase-positive isolates were detected. Pneumonia was the most frequent related nosocomial infection (67.1%) followed by UTI (23.2%). Acinetobacter baumannii (53.5%) and Klebsiella pneumoniae (40%) were the most frequently isolated pathogens. The pathogens had high rate of resistance to all antibiotics. Colistin had the most in vitro effect against all pathogens. Also, K. pneumoniae had a co-trimoxazole sensitivity rate equal to colistin (30.6%).
ConclusionCarbapenemase-positive Gram-negative bacteria causing nosocomial infections are common in our hospital and have high rate of resistance to most antibiotics. Improvement in the pattern of antibiotic use and infection control measures are necessary to overcome this resistance.
Keywords: Nosocomial infections, Carbapenemase, Antibiotic, Susceptibility -
زمینه و هدف
سودوموناس آیروژینوزا یکی از پاتوژن های گرم منفی، غیر تخمیری، کاتالاز مثبت است که باعث عفونت های مهم بیمارستانی نظیر عفونت مجاری ادراری، پنومونی، سپتی سمی می گردد. این باکتری نسبت به بسیاری از آنتی بیوتیک ها از جمله سفالوسپورین های نسل سوم مقاوم می باشد. هدف از مطالعه حاضر، بررسی شیوع ژن bla-SHV و CTX -M و تعیین فراوانی ژن های Exo A و S Exo در سودوموناس آیروژینوزای جداشده از نمونه های بالینی بیماران بستری در بیمارستان های ارومیه می باشد.
روش کاردر این مطالعه توصیفی - مقطعی، 100 جدایه سودوموناس آیروژینوزا از نمونه های بالینی خون، زخم، تراشه و ادرار بیماران بستری در بیمارستان های مختلف ارومیه جمع آوری شد. بعد از تایید باکتری با تست های بیوشیمیایی، تست حساسیت آنتی بیوتیکی با استفاده از روش انتشار دیسک انجام شد. شیوع ژن های مورد مطالعه با روش PCR استاندارد و touchdown-PCR تعیین شد.
یافته هانتایج حاصل از تست حساسیت آنتی بیوتیکی، به میزان 63% مقاومت به ژن های بتالاکتاماز و اگزوتوکسینی را نشان داد. بیشترین میزان مقاومت آنتی بیوتیکی به آنتی بیوتیک سفوتاکسیم، به میزان%86 و کمترین مقاومت نسبت به کلیستین، به میزان %3 بود. فراوانی ژ ن های CTX-M و bla-SHV و Exo S و Exo A در نمونه های مورد مطالعه، به ترتیب %93 /7، %76/4، %38/52 و %14/57 بود.
نتیجه گیریمطالعه حاضر شیوع پایینی از ژن های CTX-M وbla-SHV را در ایزوله های سودوموناس آیروژینوزا نشان داد. با توجه به اهمیت وجود سویه های مولد بتالاکتاماز و اگزوتوکسینی در بیمارستان ها، شناسایی سریع این سویه ها می تواند گامی مهم و اساسی در درمان و کنترل عفونت های ناشی از این سویه ها به شمار رود.
کلید واژگان: سودوموناس آئروژینوزا, فراوانی ژن ها, مقاومت و حساسیت آنتی بیوتیکیBackgroundPseudomonas aeruginosa is an opportunistic, gram-negative, non-fermented and catalase-positive pathogen that causes significant opportunistic infections such as urinary tract infection, pneumonia, and septicemia. P. aeruginosa is a unique bacteria that can make changes in the virulence genes expression and the rate of drug resistance in order to survive in different environments. Drug resistance resulting from beta-lactamases have been reported to be an important cause of various infections and are a critical therapeutic problem worldwide. Additionally, It has been reported that the clinical isolates of P. aeruginosa are challenging to treat because of their virulence factors and antibiotics resistances. This bacteria has a large number of pathogenic agents such as Exotoxin A, Exoenzyme S and Elastase, which causes resistance of bacteria against antibiotics. They are resistant to many antibiotics, including beta-lactams and third-generation cephalosporins. The objective of this study was to determine the prevalence of Exo A, and Exo S genes in clinical isolates of P. aeruginosa obtained from patients hospitalized in Urmia city hospitals. The other aim of this study was to evaluate the antibiotic resistance, and the prevalence of bla-SHV and CTX-M genes in clinical isolates of P. aeruginosa obtained from patients hospitalized in Urmia city hospitals.
MethodsThrough this cross-sectional and experimental-applied study, one-hundred isolates of P. aeroginosa from diverse clinical sources, including blood, wound, trachea and urine samples, were collected from different Urmia city hospitals, Iran. The hospitals and private or public laboratories were included Motahari, Imam-Reza, Arian, Taleghani, Milani, Imam-Khomeini, and Arefian. Samples were incubated and cultured in a nutrient agar culture medium at 37°C for 24 hours, and then a slide of each sample was prepared for examination by Gram Staining. Biochemical tests were performed on the samples suspected of P. aeruginosa including catalase, oxidase, oxidation/ fermentation test, pigment production, arginine dehydrolase, and growth at 42°C. Approved samples were cultured on a Mueller-Hinton agar culture medium to evaluate drug resistance. After confirmation by biochemical tests, antibiotic susceptibility test was performed using the disk diffusion method. The disks were placed at regular distances on the plateschr('39') surface, and the size of the zone of inhibition was measured after 24 hours of incubation at 37 °C. CLSI reference tables were used to detect the rate of antibiotic resistance. The antibiotic disks used in this study were included: antibiotics from the family of aminoglycosides (gentamicin, ceftriaxone, imipenem, cefotaxime, colistin and amikacin) and the β-lactam family (ceftazidime), and ciprofloxacin. In order to determine the prevalence of Exo A, Exo S, bla-SHV and CTX –M genes, DNA of the samples was extracted using the boiling method and maintained in the TE buffer in 20°C for PCR reaction. The primer sequences of the desired genes were obtained from the valid articles to perform the PCR reaction. PCR cycles were optimized, and the prevalence of genes was determined using the standard PCR method and touchdown-PCR. PCR reaction was performed at a standard volume of 25 μl. In this volume, for each microtubule, a mixture of 1 μl of extracted DNA samples, one μl of each forward and reverse primers, 12.5 μl of Master Mix and 9.5 μl of deionized distilled water were mixed. Then the PCR reaction was performed in a thermocycler with a specific time and heat cycle for amplification of each gene as follows: For the Exo A gene, the first temperature range includes an initial cycle of denaturation at 95 °C for two minutes, repetition of 14 cycles for denaturation at 95 °C for 30 seconds, annealing temperature at 73/1 °C for 30 seconds, through which the temperature decreases half a degree at each cycle, the extension temperature at 72 °C for 40 seconds. The second temperature cycle was included the denaturation at 95 °C for 30 seconds that be repeated for 19 cycles, the annealing temperature at 66.1°C for 30 seconds and the extension temperature at 72°C for 40 seconds and a final expansion cycle at 72 ° C for 40 seconds. For Exo S, bla-SHV and CTX-M genes, the temperature program was one cycle of initial denaturation at 95 ° C for two minutes, denaturation temperature at 95 °C for 30 seconds was repeated for 25 cycles, the annealing temperatures were 64°C, 61 °C and 56.7 °C respectively for 30 seconds, the extension temperature at 72 °C for 50, 70 and 80 seconds, respectively, and a final extension cycle at 72 °C for five minutes for each gene. Finally, in order to qualify the PCR product, five microliters of each sample were transferred for electrophoresis on 2% agarose gel and finally stained with ethidium bromide. The obtained data were analyzed by the qualitative method as a percentage.
ResultsIn this descriptive cross-sectional study, from 100 samples collected from different hospitals, 24 samples were obtained from the male patients (24%), and 76 samples were obtained from the female patients (76%). Clinical samples prepared from patients included 10% wounds, 4% blood and 86% urine. The antibiotic susceptibility test results indicated about 63% of resistance to β‐lactamases and exotoxin genes. The highest resistance was to cefotaxime, 86%, and the lowest resistance rate was to colisitin, 3%. The other antibioticschr('39') resistance rates were 28% for gentamicin, 61% for ceftriaxone, 28% for amikacin, 23% for ceftazidime, 24% for ciprofloxacin, and 30% for imipenem. PCR results showed 52/38% and 57/14% of the isolates contained exotoxin S and A genes, respectively. Positive genes of CTX-M and bla-SHV were detected in 7.93% and 4.76% of isolates, respectively.
ConclusionThe presence of genes encoding beta-lactamase and exotoxin enzymes and their transmission among gram-negative bacteria is a principal threat for consumers of broad-spectrum cephalosporins, especially when indiscriminate using these antibiotics. In recent decades, the emergence of resistant strains of this bacterium with multiple drug resistance has increased. Therefore, isolation and identification of P. aeruginosa from the clinical samples and reporting the results to health authorities is essential. The present study demonstrated a low occurrence of P. aeruginosa isolates carrying CTX-M and bla-SHV genes. Additionally, drug resistance and the presence of virulence factors such as exotoxins can be a severe warning for treatment centers in terms of control of disease caused by this bacterium.
Keywords: Pseudomonas aeruginosa, Gene prevalence, Antibiotic Resistance, susceptibility -
Introduction
Some communicators resort to negative appeals such as fear to encourage consumers to healthy behaviors. Nonetheless, the effectiveness of this type of content is yet questioned. Present study has been conducted to investigate how fear intensity and fear type applied in anti-obesity advertisements prompt preventive behavior among consumers.
Methods208 college students in Tehran province were randomly classified in 7 groups (6 experimental and 1 control group) based on a factorial design; 2 (fear intensity: high and low) x 3 (fear type: physical, social, and reappraisal). Research hypotheses were tested applying appropriate statistical tests including structural equation modeling and analysis of variance, based on data gathered through questionnaire and interventions such as presenting participants with visual contents.
Findingsit was revealed that there is a significant and positive relationship between the perceived severity and perceived fear, as well as between perceived susceptibility and perceived fear, and also between perceived fear and behavioral intention. Analysis of variance confirmed the significant main effect of fear intensity on behavioral intention. The main effect of the fear type on behavioral intention was not approved. However, findings indicate the significant interaction effect of fear intensity and fear type on behavioral intention so that highly intense messages that representing physical harm and lowly intense messages that representing social harm stimulate more behavioral intention.
ConclusionIt is concluded that applying fear appeal in health warning advertisements is effective in inviting consumers to healthy behavior, especially once a proper combination of the type and intensity of fear is applied in messages.
Keywords: Social marketing, Obesity, Fear appeal, Severity, Susceptibility, Behavioral intention
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