ABSTRACT
ABSTRACT Objective: To identify etiologic microbiota associated periodontal diseases among diabetes patients and the factors related to the most commonly identified bacteria species. Material and Methods: Periodontal plaque samples from 11 diabetic participants and 13 non-diabetic controls were collected to assess their aerobic and anaerobic bacterial growth. Different distinct colonies were identified by microscopic and 16srDNA sequencing. Pearson's chi-square tests were conducted to examine any association between categorical variables. Results: The diabetic subjects revealed a more intense plaque formation with a mean plaque index of 2.4 compared to 1.8 in non-diabetics. A total of 86 bacteria were isolated from 24 plaque samples, 44 were aerobic, and 42 were anaerobic. Only aerobic isolates, 22 from diabetic patients and 22 from non-diabetic patients, were evaluated in these analyses. Bacillus spp. (B. cereus mainly) and Klebsiella spp. (K. pneumoniae, K. aerogenes, K. oxytoca) were detected markedly higher in non-diabetic individuals than in diabetic subjects (p=0.026 and p=0.021, respectively). Some bacteria were only identified in the dental plaque of diabetic individuals, namely, Bacillus mojavensis, Enterobacter cloacae, Proteus mirabilis, Staphylococcus epidermidis, Staphylococcus hominis, Staphylococcus pasteuri, Streptococcus mutans, and Streptococcus pasteurianus. The presence of acid reflux and jaundice were significantly associated with the most common bacterial isolate, namely Bacillus spp., with the p-values of 0.007 and 0.001, respectively. Conclusion: Type-2 diabetes mellitus is associated with a higher amount of dental plaques. Periodontal plaque samples from diabetic and non-diabetic subjects possess differential microbial communities. Diabetic plaques contain more versatile microbes predominated by gram-positive streptococci and staphylococci.
Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Middle Aged , Aged , Periodontal Diseases/etiology , Periodontitis/pathology , Oral Health/education , Diabetes Mellitus, Type 2/microbiology , Microbiota/immunology , Streptococcus mutans/immunology , Bangladesh/epidemiology , Radiography, Dental/instrumentation , Chi-Square Distribution , Dental Care , Dental Plaque , Diabetes Mellitus/microbiologyABSTRACT
Aims: We sought to investigate norovirus burden in patients with complications of acute gastroenteritis in community level in Bangladesh. Thus, the aim of this study was to detect the incidence of norovirus in stool samples collected from study subjects with acute gastroenteritis who attended voluntarily in different community clinics at Savar area, Dhaka, Bangladesh. Methodology: The study enrolled patients from different community clinics in Savar area during July 2012 to December 2012. Stool specimens were collected in supplied stool container from patients as part of their diagnostic procedure. Viral RNA was extracted from the samples using the QIAamp® viral RNA mini kit (Qiagen, Germany). Real-time RT-PCR assay was conducted to identify different norovirus genogroups in the stool samples. Results: We detected norovirus exclusively in 23.8% (10/42) of the stool samples where rotavirus was absent. Over 80% patients were aged less than 2 years and all 10 norovirus-positive samples were detected within this age range (P = 0.17). Detection rates for norovirus was the highest in July and the lowest in November among the months covered in the study. Genogroup analysis of detected noroviruses showed 1(10%) as GI, 8 (80%) as GII and the remaining 1 (10%) as the mixture of GI and GII genogroups. Conclusions: This study has provided baseline incidence of norovirus diarrhea in patients attended at community hospitals in Savar area, Dhaka, Bangladesh. The infections were exclusively in children aged less than two years. Norovirus genogroup-II was predominant in the community infections covered under this study.