Effects of selection and compiling strategy of substrates in column-type vertical-flow constructed wetlands on the treatment of synthetic landfill leachate containing bisphenol A.

A constructed wetland (CW) is a low-cost, eco-friendly, easy-to-maintain, and widely applicable technology for treating various pollutants in the waste landfill leachate. This study determined the effects of the selection and compiling strategy of substrates used in CWs on the treatment performance of a synthetic leachate containing bisphenol A (BPA) as a representative recalcitrant pollutant. We operated five types of lab-scale vertical-flow CWs using only gravel (CW1), a sandwich of gravel with activated carbon (CW2) or brick crumbs (CW3), and two-stage hybrid CWs using gravel in one column and activated carbon (CW4) or brick crumbs (CW5) in another to treat synthetic leachate containing BPA in a 7-d sequential batch mode for 5 weeks. CWs using activated carbon (CW2 and CW4) effectively removed ammonium nitrogen (NH4-N) (99-100%), chemical oxygen demand (COD) (93-100%), and BPA (100%), indicating that the high adsorption capacity of activated carbon was the main mechanism involved in their removal. CW5 also exhibited higher pollutant removal efficiencies (NH4-N: 94-99%, COD: 89-98%, BPA: 89-100%) than single-column CWs (CW1 and CW3) (NH4-N: 76-100%, COD: 84-100%, BPA: 51-100%). This indicates the importance of the compiling strategy along with the selection of an appropriate substrate to improve the pollutant removal capability of CWs.

Development of a Quantitative PCR Assay for Arcobacter spp. and its Application to Environmental Water Samples.

Arcobacter spp. are emerging pathogens associated with gastroenteritis in humans. The objective of this study was to develop a highly sensitive and broadly reactive quantitative PCR (qPCR) assay for Arcobacter spp. and to apply the developed assay to different water sources in the Kathmandu Valley, Nepal. Fifteen samples to be analyzed by next-generation sequencing were collected from 13 shallow dug wells, a deep tube well, and a river in the Kathmandu Valley in August 2015. Among the 86 potential pathogenic bacterial genera identified, Acinetobacter, Pseudomonas, Flavobacterium, and Arcobacter were detected with relatively high abundance in 15, 14, 12, and 8 samples, respectively. A primer pair was designed with maximal nucleotide homologies among Arcobacter spp. by comparing the sequences of 16S rRNA genes. These primers were highly specific to most of the known species of Arcobacter and quantified between 1.0×101 and 6.4×106 copies reaction-1 and sometimes detected as few as 3 copies reaction-1. The qPCR assay was used to quantify Arcobacter spp. in bacterial DNA in not only the above 15 water samples, but also in 33 other samples collected from 15 shallow dug wells, 6 shallow tube wells, 5 stone spouts, 4 deep tube wells, and 3 springs. Thirteen (27%) out of 48 samples tested were positive for Arcobacter spp., with concentrations of 5.3-9.1 log copies 100 mL-1. This qPCR assay represents a powerful new tool to assess the prevalence of Arcobacter spp. in environmental water samples.

Bacterial meningitis in children under 15 years of age in Nepal.

BACKGROUND: Bacterial meningitis in children is a life-threatening problem resulting in severe morbidity and mortality. For the prompt initiation of antibacterial therapy, rapid and reliable diagnostic methods are of utmost importance. Therefore, this study was designed to find out the rate of bacterial pathogens of meningitis from suspected cases by performing conventional methods and latex agglutination. METHODS: A descriptive type of study was carried out from May 2012 to April 2013. Cerebrospinal fluid (CSF) specimens from 252 suspected cases of meningitis were subjected for Gram staining, bacterial culture and latex agglutination test. The identification of growth of bacteria was done following standard microbiological methods recommended by American Society for Microbiology. Antibiotic sensitivity testing was done by modified Kirby-Bauer disk diffusion method. RESULTS: From the total 252 suspected cases, 7.2 % bacterial meningitis was revealed by Gram staining and culture methods whereas latex agglutination method detected 5.6 %. Gram-negative organisms contributed the majority of the cases (72.2 %) with Haemophilus influenzae as the leading pathogen for meningitis. Overall, 33.3 % mortality rate was found. CONCLUSIONS: In conclusion, a significant rate of bacterial meningitis was found in this study prompting concern for national wide surveillance.