Prevalence of House Dust Mites and Presence of Der p 1 and Der f 1 in Ordu, Giresun, Trabzon and Rize Provinces.

OBJECTIVE: This study was carried out to detect house dust mites in houses and to investigate group 1 antigens of Dermatophagoid species in Ordu, Giresun, Trabzon and Rize provinces of the Central and Eastern Black Sea Region. METHODS: Dust samples obtained from the beds were subjected to both microscopic and antigenic examination. Samples prepared by the lactic acid method for microscopic examination were evaluated under a light microscope. Antigenic analysis was performed by investigating Der p 1 and Der f 1 belonging to D. pteronyssinus and D. farinae by ELISA test. RESULTS: 90.3% of the dust samples were evaluated positive by microscopic examination (10x, 40x) and 149 mites were detected. D. pteronyssinus 74%, D. farinae 13%, Dermatophagoides spp. growth forms 5%, Cheyletus spp. 1%, E. maynei 1%, C. arcuatus 1%, T. putrescentiae 1%, L. destructor 1% and unidentified mites were detected at the rate of 3% respectively. Der p 1 antigen was detected in 93% and Der f 1 antigen in 84.7%. The highest amount of antigen detected in one gram of powder was 1,272 µg for Der p 1 and 0,482 µg for Der f 1. CONCLUSION: No difference was observed between mite species and distribution in the provinces where the study was conducted (p<0.05). Dermatophagoides were found in 93% of the population. The low (4%) rate of storage/food mites is related to the fact that samples were not taken from the floors. Antigen accumulation may be important in the beds since the activity of the mites is observed throughout the year in temperate and humid regions. It is thought that this diagnosis method can be used and can be taken into account in terms of the environments in which sensitive people live.

The Investigation of the Prevalance and Epidemiology of House Dust Mites in Giresun

Objective: The aim of this study was to determine the species of house dust mites and their prevalence in Giresun. Methods: Dust samples taken from 15 houses which were visited monthly for one year were examined by the lactic acid method. Results: A total of 2251 mites were detected in the study. The distribution of mites was as follows: 81.8% Dermatophagoides pteronyssinus, 0.5% Dermatophagoides farinae, 0.04% Euroglypus maynei (E. maynei), 4.2% Dermatophagoides spp. 0.06% A. siro, 2.4% Glycphagus domesticus, 0.9 % Lepidoglyphus destructor, 1.4% Tyrophagus putrescentiae, 4.5% Campunatus arcuatus, 1.3% Cheyletus spp. Pyroglyphid species were detected in all houses (100%). Dermatophagoides pteronyssinus was found in 100%, D. farinae 5% and E. maynei 4% of the houses. Conclusion: The mites in Giresun were found in all houses throughout the year and were detected in all of the samples. Although they were detected in greater amounts in the spring and summer, only a moderate relationship could be detected with temperature. In August-October period, mite existence was significantly higher than the January-March period (p<0,05). D. pteronyssinus was found in higher numbers on the mezzanine floors between May and August and on the ground floors in September and October (p<0,05). We think that the climate characteristics of Giresun are suitable for the development and proliferation of house dust mites and this can pose a risk for sensitive people.

The Investigation of the Presence of Mites in Some Served Dry Foodstuffs.

OBJECTIVE: Mites are microscopic organisms that lower the quality of life of people who are sensitive to them by causing conditions such as atopic dermatitis, allergic rhinitis, and asthma. These organisms are found in every habitat where humans live. This study was conducted to determine the presence of storage mites in dry food items. METHODS: Various food items were procured 10 times each in 300-gram samples. Mites were extracted with a Berlese funnel apparatus over Erlenmeyer flasks containing 70% alcohol placed at the end of the funnel stems for over 48 h. RESULTS: Of 25 food items examined in the study, only six were contaminated by mites. Species of the mites found were Acarus siro (34.6%), Glycyphagus domesticus (22.8%), Tyrophagus putrescentiae (16.8%), Tyrophagus spp. (7.9%), Rhizoglyphus spp. (1%), Lepidoglyphus destructor (7.9%), Cheylettus malacensis (4%), and Cheylettus spp. (2%). CONCLUSION: Although the results of the study show that the presence of mites in food items sold in open containers at open-air markets or stores was low, we suppose that they can cause important health problems for sensitive people.

[Genotypic identification and distribution patterns of Candida parapsilosis complex species (C.parapsilosis sensu stricto, C.metapsilosis and C.orthopsilosis) isolated from clinical samples]. / Klinik Örneklerden Izole Edilen Candida parapsilosis Kompleks Türlerinin (C.parapsilosis sensu stricto, C.metapsilosis ve C.orthopsilosis) Genotipik Olarak Tanimlanmasi ve Dagilimlarinin Belirlenmesi.

Candida parapsilosis, which has recently gained increasing importance, is the second most common fungal pathogen isolated from clinical specimens. C.parapsilosis strains exhibiting genetic heterogeneity were previously considered as a complex of three genetically different groups (group I, II, III). However, they have recently been reclassified as new species and named as C.parapsilosis sensu stricto (Grup I), C.orthopsilosis (Grup II) and C.metapsilosis (Grup III). In the present study we aimed to identify C.parapsilosis complex species by PCR-RFLP (Polymerase chain reaction-Restriction fragment lenght polymorphism) method and to determine the distribution of new species isolated from clinical specimens. A total of 68 samples (44 blood, 10 urine, 5 wound, 2 paracentesis fluids, 2 tympanocentesis samples and one of each cerebrospinal fluid, peritoneal fluid, surgical material, oral lesion and nail sample) in which C.parapsilosis had been isolated and identified with API 20C AUX (bioMérieux, France) between October 2005 - July 2009 in the Microbiology Laboratory of Karadeniz Technical University Hospital, in Trabzon, Turkey, were included in the study. Yeast genomic DNA was extracted using the "High Pure PCR Template Preparation Kit" (Roche Diagnostic, USA) and amplification of SADH gene was performed by using specific primers (S1-F sense; 5'-GTTGATGCTGTTGGATTGT-3' ve S1-R antisense; 5'-CAATGCCAAATCTCCCAA-3') with PCR. RFLP method was then applied by digesting PCR product (716 bp) with BanI enzyme (Fermentas, USA). In our study 98.5% (67/68) of the isolates were identified as C.parapsilosis sensu stricto, and 1.5% (1/68) was identifed as C.orthopsilosis, whereas no C.metapsilosis strains were detected. The strain identified as C.orthopsilosis was from a urine specimen and all the blood culture isolates were C.parapsilosis sensu stricto. In conclusion, the inability to differentiate C.parapsilosis complex species by phenotypical and routine tests leads to lack of knowledge in the clinical importance, isolation rates and geographical distribution of these species. Thus, genotypical identification of C.parapsilosis complex species will be the initial step for the arrangement of further studies in that area.