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1.
Acta Gastroenterol Belg ; 82(2): 285-290, 2019.
Article in English | MEDLINE | ID: mdl-31314190

ABSTRACT

BACKGROUND AND AIM: Intestinal barrier dysfunction has been implicated in the development of infectious complications of acute pancreatitis. Nucleotide-Binding Oligomerization DomainContaining Protein 2 (NOD2) plays an important role in the proper functioning of intestinal defense mechanisms. Here, we investigated the frequency of NOD2 variants in patients with mild and severe acute pancreatitis. MATERIALS AND METHODS: Groups 1, 2 and 3 comprised healthy participants and patients with mild and severe pancreatitis, respectively. Four NOD2 variants and serum interleukin-6 (IL-6), Tumor Necrosis Factor-a (TNF-a) and lipopolysaccharide-binding protein (LBP) levels were analyzed. RESULTS: Three patients (3/32, 9.4%) in the severe pancreatitis group were positive for the p.R702W variant. This variant was negative in other groups. One, three and three patients in the healthy (1/27, 3.7%), mild (3/36, 8.3%) and severe pancreatitis (3/32, 9.4%) groups tested positive for the 1007fs variant, respectively. No significant differences in the frequencies of NOD2 variants were evident among the groups. Serum IL-6, TNF-a and LBP levels were markedly higher in the severe pancreatitis than the healthy and mild pancreatitis groups (all p<0.001). We observed no significant correlation between cytokine levels and NOD2 variants. CONCLUSION: Our results support an association between the presence of the p.R702W variant and severe pancreatitis.


Subject(s)
Carrier Proteins/blood , Interleukin-6/blood , Membrane Glycoproteins/blood , Nod2 Signaling Adaptor Protein/metabolism , Pancreatitis/blood , Tumor Necrosis Factor-alpha/blood , Acute Disease , Acute-Phase Proteins/metabolism , Carrier Proteins/metabolism , Case-Control Studies , Healthy Volunteers , Humans , Interleukin-6/metabolism , Intestines , Membrane Glycoproteins/metabolism , Nucleotides , Pancreatitis/diagnosis , Severity of Illness Index , Tumor Necrosis Factor-alpha/metabolism
2.
J Mycol Med ; 27(3): 376-381, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28641919

ABSTRACT

INTRODUCTION: Candida africana and C. dubliniensis are closely related species of C. albicans. Current phenotypic methods are not suitable to accurately distinguish all the species belonging to the C. albicans complex. Several molecular-based methods have recently been designed for discriminating among closely related Candida species. The aim of this study was to establish the prevalence of C. dubliniensis and C. africana in vulvovaginal samples with phenotypic and genotypic methods. MATERIALS AND METHODS: We re-examined 376 vulvovaginal C. albicans complex isolates. All the isolates were identified with morphological features and HWP1 gene polymorphisms. ITS and D1/D2 sequencing, carbohydrate assimilation, MALDI-TOF MS profiles and antifungal susceptibilities were evaluated for C. africana and C. dubliniensis isolates. RESULTS: Of the 376 isolates, three C. africana and three C. dubliniensis isolates (0.8% and 0.8% prevalence, respectively) were identified by molecular methods (HPW1, ITS and D1/D2) Phenotypically, C. africana differed from C. albicans and C. dubliniensis by formation of no/rare pseudohyphae, absence of chlamydospores and, the development of turquoise green colonies on CHROMagar. MALDI-TOF MS and API ID 32C could not revealed C. africana isolates. C. africana and C. dubliniensis isolates showed very low MIC values for all the tested antifungals. DISCUSSION: This first report of C. africana from Turkey provides additional data for epidemiological, phenotypic features and antimicrobial susceptibility profiles. This study also highlights the importance of using genotypic methods in combination with phenotypic methods.


Subject(s)
Candida/isolation & purification , Candidiasis, Vulvovaginal/epidemiology , Candidiasis, Vulvovaginal/microbiology , Candida/classification , Candida/genetics , DNA, Fungal/analysis , Female , Humans , Microbial Sensitivity Tests , Mycological Typing Techniques , Prevalence , Sequence Analysis, DNA , Turkey/epidemiology
3.
Ann Trop Med Parasitol ; 105(5): 359-65, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21929877

ABSTRACT

In this study, we aimed to study the molecular and epidemiological characteristics of Salmonella enterica serovar Typhi (S. Typhi) outbreak in Eastern Anatolia. Six hundred and thirty-seven patients from the same county with clinical diagnosis of typhoid fever were investigated with conventional methods from stool, urine and blood specimens. Antibiotic susceptibility tests and identifications were performed for positive specimens. Clonal relationships between the isolates were investigated using pulsed field gel electrophoresis (PFGE) method. A questionnaire was completed for the water consumption habits of patients. Of 91 culture positive specimens, 76 were blood, 13 were stool and 2 were urine. The isolates were resistant to ampicillin, ampicillin/sulbactam, chloramphenicol, cefuroxime, amikacin, gentamicin and trimethoprim-sulfamethoxazole. Although there was a single band difference in some isolates, PFGE results indicated that this was an outbreak caused by single strain according to the Tenover criteria. This outbreak thought to be associated with the consumption of tap water contaminated with sewage represents a breakdown of the basic public health and civil engineering infrastructure. Appropriate public health measures should be taken in order to avoid such outbreaks in the future.


Subject(s)
Disease Outbreaks , Food Microbiology , Salmonella typhi/isolation & purification , Typhoid Fever/epidemiology , Typhoid Fever/transmission , Water Microbiology , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , Drug Resistance, Bacterial , Electrophoresis, Gel, Pulsed-Field , Feces/microbiology , Female , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Public Health/standards , Surveys and Questionnaires , Turkey/epidemiology , Typhoid Fever/microbiology , Young Adult
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