Microbial Quality and Public Health Risks of Selected Herbal Remedies Sold in Open Markets in Owerri Metropolis, South Eastern, Nigeria

Herbal medicines are presently widely used in developed and developing countries for health care due to their affordability, accessibility and availability. Objective: The microbial quality of selected herbal remedies sold in open markets in Owerri, South Eastern, Nigeria was studied. Methods: The samples were bulked according to type and then serially diluted. The spread plate technique was used in inoculating the samples on the appropriate culture medium and then incubated. Standard laboratory protocols for microbiological studies and biochemical tests were employed for the identification of the microorganisms present in the samples. Results: The presence of bacterial species namely Bacillus, Corynebacterium, Micrococcus, Enterococcus and Staphylococcus spp was recorded. They were all gram positive and bacterial counts ranged from 1.0 x 106 to 7.8 x 107cfu/ml. Fungal isolates included Mucor, Saccharomyces and Penicillium spp. and fungal counts ranged from 3.0x103 to 1.3x108 cfu/ml respectively. Conclusion: The presence of these microorganisms in herbal remedies do not only make them hazardous, but might also change the physical, chemical and natural properties of the herbal remedies by altering the contents of active ingredients or converting them to toxic products. The production and consumption of herbal remedies should be properly supervised and monitored to ensure that only good quality products get to the consumers.

Isolation and Screening of Mannanase Producing Bacteria from Agricultural Wastes.

Aim: The work focused on the isolation and screening of mannanase-producing bacteria associated with selected agricultural wastes. Study Design: The first experiment, mannanase-producing bacteria were screened for mannanase production on Locust Bean Gum (LBG) agar medium and total bacterial count was determined. In the second experiment, the isolated bacteria were further screened for mannanase production in submerged state fermentation. Place and Duration of Study: Microbiology Research Laboratory Federal University of Technology, Akure and Postgraduate Research Laboratory, Obafemi Awolowo University Ile-Ife, Nigeria between September 2011 and March 2012. Methodology: The associated bacterial isolates were isolated on agar medium containing LBG and counted by standard microbiological methods. Quantitatively, mannanase production was conducted in mineral salt medium into which copra meal had been incorporated as the sole carbon source and enzyme activity was determined by dinitrosalicylic acid method. Results: The highest bacteria counts were recorded in compost from wood dust with 5.5×1011 cfu/g, while cassava peels had the least of 1.02×106 cfu/g. In this study, 23 bacterial isolates showed positive results with clear zone around the cultures. Bacterial isolate 1A showed the highest ratio of clear zone to colony, while the lowest was observed in isolate 4B. In liquid broth, all the 23 isolates displayed mannanase activity between 0.28 to13.89 U/ml for static and 0.56 to 13.43 U/ml for shaken condition, with the highest mannanase activity observed with isolate IA for both culture conditions. In the comparative study between static and shaken conditions, it was revealed that shaken cultures exhibited better yield than static cultures. According to the morphological and biochemical studies, the isolate 1A was primarily identified as the Klebsiella edwardsii. Conclusion: In this investigation, bacterial isolates evaluated for mannanase production from agricultural wastes elaborated considerable mannanase activity and this could be applied in feed and prebiotic.

Yields from blood cultures of patients with suspected paratyphoid fever A

The yield and speed of detection of Salmonella enterica serotype Paratyphi A from the blood of patients with suspected paratyphoid fever A in 13 500 paired aerobic and anaerobic bottles (AEB, ANB) that were each filled with 5 ml of blood by the BacT/ALERT 3D system were compared, and the blood bacterial counts of 1 000 probable patients were estimated by pour plate method. A total of 4 060 isolates were recovered, of these, 3 149 were recovered from both AEB and ANB, 461 from the AEB only, and 450 from the ANB only. The estimating median bacterial count in blood from 400 patients was 0.5 CFU/ml. The research findings demonstrate that the blood volume drawn is an important factor determining the yields from blood cultures. Growth of significantly more isolates was detected earlier in AEB.

Effect of saline irrigation used in combination with antimicrobial agents on salivary bacterial counts

INTRODUCTION: The aim of the present study was to investigate the effect of mechanical irrigation in combination with mouthwash of antimicrobial agents on salivary bacterial counts. MATERIALS AND METHODS: This study was performed with a randomized study employing a panel of 40 healthy volunteers (20 males and 20 females) between the age of 26 and 32 years. Volunteers were randomly put in one of four treatment groups. In the first group, 0.2 mL of non-stimulatory saliva was collected from every subjective person. Then, saliva was collected after rinsing with chlorhexidine (CHX) for 1 minute. In the second group, non-stimulatory saliva was collected, and then saliva was collected after rinsing with CHX and irrigation with saline. In the third and fourth groups, the same procedures as the first and second groups were performed with povidone iodine (PVI) instead of CHX. All of these samples were cultured for 48 hours aerobically. The reduction rates of colony-forming units (CFU) were calculated for each group. The reduction rate between each group was tested statistically using student t-test. RESULTS: Using CHX in combination with saline irrigation showed a significant decrease of the salivary bacterial CFU when compared with only using CHX.(P0.01) CONCLUSION: It was concluded that the CHX or PVI used with saline irrigation made the salivary bacterial counts reduced more than when CHX or PVI was used alone as an oral antiseptic agent.

Salivary Bacterial Counts after Application of Povidone-Iodine and Chlorhexidine

OBJECTIVE: It is important to sterilize oral cavity with antibacterial agent before surgery for preventing infection. The object of this study was to compare the effect on reduction of salivary bacterial counts according to applied time when povidone-iodine (PVI) and chlorhexidine gluconate (CHX), most broadly used materials in dentistry, were applied intraorally before the surgery. METHODS: Sixty subjects were divided into 6 groups. PVI and CHX were applied in each group for 1, 2 and 3 minutes, respectively. Then salivary microbacteria taken before and after applying the materials were cultured using 5% sheep blood agar plate. RESULTS: There was significant difference in reduction of microbacteria in both PVI and CHX and the effect did not show differences depending on time. When applied for a minute, PVI showed somewhat higher reduction rate than CHX, but in the other groups, there was no difference in reduction rate. CONCLUSION: We found that there was no significant difference in sterilization ability of PVI and CHX in all groups in this study. Therefore, both agents would get sufficient effect when applied for a minute.

Salivary Bacterial Counts after Application of Povidone-Iodine and Chlorhexidine

OBJECTIVE: It is important to sterilize oral cavity with antibacterial agent before surgery for preventing infection. The object of this study was to compare the effect on reduction of salivary bacterial counts according to applied time when povidone-iodine (PVI) and chlorhexidine gluconate (CHX), most broadly used materials in dentistry, were applied intraorally before the surgery. METHODS: Sixty subjects were divided into 6 groups. PVI and CHX were applied in each group for 1, 2 and 3 minutes, respectively. Then salivary microbacteria taken before and after applying the materials were cultured using 5% sheep blood agar plate. RESULTS: There was significant difference in reduction of microbacteria in both PVI and CHX and the effect did not show differences depending on time. When applied for a minute, PVI showed somewhat higher reduction rate than CHX, but in the other groups, there was no difference in reduction rate. CONCLUSION: We found that there was no significant difference in sterilization ability of PVI and CHX in all groups in this study. Therefore, both agents would get sufficient effect when applied for a minute.