Harmful cyanobacterial toxic blooms in waste stabilisation ponds

2000 ◽  
Vol 42 (10-11) ◽  
pp. 179-186 ◽  
Author(s):  
B. Oudra ◽  
M. El Andaloussi ◽  
S. Franca ◽  
P. Barros ◽  
R. Martins ◽  
...  

A coccoid picocyanobacterium Synechocystis sp. (0.6-2 μm of cell diameter) was found to be dominant during summer period in the experimental wastewater stabilisation pond of Marrakesh. The taxonomy of this isolated strain was confirmed by electron microscope study. The general patterns of ultrastructure and the mode of cell division resemble Chroococcales. The cyanobacterium strain was axenic and cultured on both inorganic Z8 and BG13 media. Mammalian toxicity was confirmed by mice bioassay. The major sympton of poisoning was severe diarrhoea. Histopathological study shows a slight hepatotoxicosis associated with a pronounced change in the intestinal mucosa which shows swelling and destruction of villi epithelium and shedding of enterocytes into the lumen. Although slow, these kinds of poisoning are comparable to those induced by okadiac acid intraperitoneal mice injection (diarrhetic shellfish poisoning “DSP” toxins). By using the enzyme-linked immunosorbent assay (ELISA), the amount ofhepatotoxins “microcystins” was determined. The result shows that Synechocystis can produce a small amount of total microcystine [an average of 15 μg−1 dry weight corresponding to 20 ng(109cell)−1]. These findings lead us to consider Synechocystis as both a potent neurotoxin and hepatotoxin producer. Because of the confirmed cyanobacterium toxicity, an eventual ecological implication should be considered. However, a toxic chronic test experiment on Daphnia was simultaneously carried out. Juvenile D. magna (less than 24 hours old), were fed three concentrations (104, 106, 108 cells / ml) of Synechocystis. A group of organisms fed with Chlorella vulgaris (3. 105 cells/ml) and another group without food, were studied as control treatments. Only animals cultured with 104 cells/ml of cyanobacterium survived at 80% until the end of the test (21 days). Reproduction and normal growth occurred in control treatments fed with Chlorella vulgaris and the group fed with the lowest concentration of Synechocystis. One-way ANOVA statistical analyses show significant differences in Daphnia survival and growth, between treatments with and without Synechocystis and between treatments with and without food. In terms of this study, there is evidence that toxic picocyanobacteria blooms occurring in wastewater stabilization ponds of Marrakesh, could have harmful repercussions on zooplanktonic, bacteria and other algae communities. Consequently, this will constitute a possible hindrance for sewage self-purification process and system treatment performance. In addition, the reuse of such treated wastewater effluent for irrigation will constitute an additional, potent, health hazard for animals and human's.

Author(s):  
В.Я. Кофман

Пандемия СOVID-19, объявленная ВОЗ чрезвычайной ситуацией в области здравоохранения, вызвана новым коронавирусом SARS-CoV-2. По сообщениям из Евросоюза, США и Австралии, потенциальная выживаемость коронавируса SARS-CoV-2 в фекалиях и сточных водах в течение достаточно длительного времени создает реальную возможность его поступления с канализационными стоками на очистные сооружения или непосредственно в поверхностные воды при сбросе неочищенных стоков. Это свидетельствует о существовании потенциальной возможности передачи SARS-CoV-2 через воду. В этой связи особую актуальность приобретает разработка эффективных способов удаления и инактивации вирусов на очистных сооружениях. Наличие коронавирусной инфекции в сточных водах может представлять серьезную опасность для здоровья контактирующих с ними людей. К ним относится персонал очистных сооружений, а также население в целом, которое может подвергаться непосредственному воздействию необработанных или недостаточно обработанных сточных вод через неисправные водопроводные или канализационные коммуникации. Во многих странах для получения своевременной достоверной информации о распространении коронавирусной инфекции используют методы эпидемиологии сточных вод. Возможность выявления РНК вируса в сточных водах даже при низкой распространенности СOVID-19 и корреляция между концентрацией РНК SARS-CoV-2 в сточных водах и официальной информацией указывают на то, что наблюдение за сточными водами может стать чувствительным инструментом мониторинга циркуляции вируса в популяции. The COVID-19 pandemic, declared by WHO as a health emergency, is caused by a novel SARS-CoV-2 coronavirus. According to reports from the European Union, the United States and Australia, the potential survival of the SARS-CoV-2 coronavirus in feces and wastewater for a sufficiently long time creates a real threat of its entry with wastewater into treatment facilities or directly into surface water while raw wastewater is discharged. This indicates the potential for the transfer of SARS-CoV-2 by water. In this regard, the development of effective methods for the removal and inactivation of viruses at the treatment facilities is of special actuality. The presence of coronavirus infection in wastewater can pose a serious health hazard to people in contact with it. These include the personnel at the wastewater treatment facilities, as well as the general population, who may be directly exposed to raw or inadequately treated wastewater through defective water or sewer systems. In many countries wastewater epidemiology methods are used to obtain timely reliable information on the spread of coronavirus infection. Possible detection of RNA virus in wastewater even with a low prevalence rate of COVID-19 and the correlation between the concentration of SARS-CoV-2 RNA in wastewater and official information indicate that monitoring wastewater can become a sensitive tool for monitoring the circulation of the virus in the population.


2014 ◽  
Vol 11 (2) ◽  
pp. 107-112 ◽  
Author(s):  
SK Dey ◽  
MS Rahman ◽  
UK Rima ◽  
MZ Hossain ◽  
GA Chowdhury ◽  
...  

Brucellosis is a widespread and economically important infectious disease of animals and humans caused by the members of the genus Brucella. The disease is manifested by abortion, birth of unthrifty calves and retained placentae in female animals. The correct and prompt diagnosis is important for controlling and eradicating the disease from animals. This experiment was carried out in the Department of Pathology, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh to detect Brucella antibody in dairy cows using Rose Bengal Plate Test (RBPT), indirect Enzyme Linked Immunosorbent Assay (i-ELISA) and histopathology. The study was carried out between the periods of January 2012 to September 2012. Placental tissue obtained from aborted cow and internal organs of aborted fetus were used in histopathological study. A total of 190 sera sample were collected with the history of reproductive disorders, like late abortion, retained placenta and anestrous from Veterinary Hospital, Bangladesh Agricultural University (BAU) and meat market Kewatkhali, Mymensingh. The seroprevalance of brucellosis using RBPT and iELISA were 2.63% and 1.05% respectively. Histopathological study revealed multifocal necrosis in hepatic parenchyma, depletion of lymphocytes in spleen and lymphnodes and distended trabeculi in spleen and lymphnodes in aborted calf, diffuse fibrosis around the placental epithelia and in placental tissues. Distinct histopathological lesions in the liver and spleen of Brucella suspected calf were not evident but the retained fetal membrane showed characteristics fibrosis and reactive cellular infiltration. It needs to adopt nucleic acid based technologies in order to confirm the species of Brucella involved and as well as to avoid cross reactivity of antibodies as seen in RBPT and iELISA.DOI: http://dx.doi.org/10.3329/bjvm.v11i2.19124 Bangl. J. Vet. Med. (2013). 11 (2): 107-112


2015 ◽  
Vol 113 (2) ◽  
pp. 404-409 ◽  
Author(s):  
Tobias Dörr ◽  
Laura Alvarez ◽  
Fernanda Delgado ◽  
Brigid M. Davis ◽  
Felipe Cava ◽  
...  

The bacterial cell wall is critical for maintenance of cell shape and survival. Following exposure to antibiotics that target enzymes required for cell wall synthesis, bacteria typically lyse. Although several cell envelope stress response systems have been well described, there is little knowledge of systems that modulate cell wall synthesis in response to cell wall damage, particularly in Gram-negative bacteria. Here we describe WigK/WigR, a histidine kinase/response regulator pair that enablesVibrio cholerae, the cholera pathogen, to survive exposure to antibiotics targeting cell wall synthesis in vitro and during infection. Unlike wild-typeV. cholerae, mutants lackingwigRfail to recover following exposure to cell-wall–acting antibiotics, and they exhibit a drastically increased cell diameter in the absence of such antibiotics. Conversely, overexpression ofwigRleads to cell slimming. Overexpression of activated WigR also results in increased expression of the full set of cell wall synthesis genes and to elevated cell wall content. WigKR-dependent expression of cell wall synthesis genes is induced by various cell-wall–acting antibiotics as well as by overexpression of an endogenous cell wall hydrolase. Thus, WigKR appears to monitor cell wall integrity and to enhance the capacity for increased cell wall production in response to damage. Taken together, these findings implicate WigKR as a regulator of cell wall synthesis that controls cell wall homeostasis in response to antibiotics and likely during normal growth as well.


2004 ◽  
Vol 3 (2) ◽  
pp. 385-392 ◽  
Author(s):  
Javier García-Rivera ◽  
Yun C. Chang ◽  
K. J. Kwon-Chung ◽  
Arturo Casadevall

ABSTRACT Several genes are essential for Cryptococcus neoformans capsule synthesis, but their functions are unknown. We examined the localization of glucuronoxylomannan (GXM) in strain B-3501 and in cap59 mutants B-4131 and C536. Wild-type strain B-3501 showed a visible capsule by India ink staining and immunofluorescence with anticapsular monoclonal antibodies (MAbs) 12A1 and 18B7. B-4131, a mutant containing a missense mutation in CAP59, showed no capsule by India ink staining but revealed the presence of capsular polysaccharide on the cell surface by immunofluorescence. The cap59 gene deletion mutant (C536), however, did not show a capsule by either India ink staining or immunofluorescence. Analysis of cell lysates for GXM by enzyme-linked immunosorbent assay revealed GXM in C536 samples. Furthermore, the epitopes recognized by MAbs 12A1, 2D10, 13F1, and 18B7 were each detected in the cytoplasm of all strains by immunogold electron microscopy, although there were differences in location consistent with differences in epitope synthesis and/or transport. In addition, the cells of B-3501 and B-4131, but not those of the cap59 deletant, assimilated raffinose or urea. Hence, the missense mutation of CAP59 in B-4131 partially hampered the trafficking of GXM but allowed the secretion of enzymes involved in hydrolysis of raffinose or urea. Furthermore, the cell diameter and volume for strain C536 are higher than those for strain B-3501 or B-4131 and may suggest the accumulation of cellular material in the cytoplasm. Our results suggest that CAP59 is involved in capsule synthesis by participating in the process of GXM (polysaccharide) export.


2010 ◽  
Vol 4 (1) ◽  
pp. 20-27
Author(s):  
Noor Hashim ◽  
Khulood Al-Samarrae ◽  
Salim Al-Obaidy

Trichothecenes are natural secondary metabolites causing economic losses and health hazard to human and farm animals which are produced by several species of Fusarium and some other genera on different agricultural commodities. Study on trichothecenes mycotoxicosis revealed morphological, biochemical, and histopathological changes. After intraperitoneal injection of the toxin in male mice with different concentration for 35 days shows marked increase in body weight, dyspanea, shivering, bristling up of hair, hair falling, anomalies of eyes, and irritation around neck, also abdominal hemorrhage and clot accumulation in abdomen. In addition to inclusion (retention) cyst forms on liver. The biochemical studies on liver function by measuring GPT and GOT enzymes level have been done. An increase level of these enzymes in treated animal in comparison with control animal which indicating abnormal function of liver observed. The histopathological study on sections from the liver of treated animal with trichothecenes revealed many alterations in liver which includes congestion, kupffer cells hyperplasia, dilated sinusoids and mononuclear cells infiltration around the portal area.


1995 ◽  
Vol 78 (6) ◽  
pp. 1403-1407 ◽  
Author(s):  
Eoin P Carmody ◽  
Kevin J James ◽  
Seán S Kelly

Abstract Dinophysistoxin-2 (DTX-2), an isomer of okadaic acid (OA), recently has been found in Irish waters. DTX-2 was the predominant toxin during prolonged infestations in cultivated mussels along the southwest coast of Ireland. Substantial variations in toxin levels may exist both horizontally and vertically in the water column. The need to take multiple samples and the ethical concern about the use of mammals for routine quality control of shellfish prompted examination of 2 commercially available enzyme-linked immunosorbent assay (ELISA) methods, designed to detect OA, for determination of both OA and DTX-2. One ELISA method (DSPCheck, Sceti Co. Ltd., (Tokyo, Japan) showed good cross-reactivity (40 ± 5%) with standard DTX-2. This study showed that both ELISA methods show good correlation with the liquid chromatographic analysis of 9-anthryldiazomethane derivatives when OA is the predominant toxin present. The sensitivity was also good for OA determination using both methods, which allowed toxin measurement at 10 ng/mL (0.5 ng/well). This level is equivalent to 0.03 μg/g mussel meat. Blank mussel samples spiked with DTX-2 standards gave a good linear correlation (r = 0.997) with this ELISA method when toxin levels were 0.03-0.3 μg/g mussel meat. This range is appropriate for regulatory control of diarrhetic shellfish poisoning.


2007 ◽  
Vol 90 (4) ◽  
pp. 1000-1010 ◽  
Author(s):  
Hans Kleivdal ◽  
Sven-Inge Kristiansen ◽  
Mona V Nilsen ◽  
Lyn Briggs

Abstract Method validation was conducted for an enzyme-linked immunosorbent assay (ELISA) for the determination of domoic acid (DA) toxins, known to give amnesic shellfish poisoning (ASP) symptoms, in shellfish. The calibration curve range of the assay is approximately 10260 pg/mL, with a dynamic working range for DA toxins in shellfish from 0.01 to at least 250 mg/kg. The ASP ELISA showed no significant cross-reactivity to structural analogs, and proved to be robust to deliberate alterations of the optimal running conditions. The shellfish matrix effects observed with mussels, oysters, and scallops were eliminated by diluting shellfish extracts 1:200 prior to analysis, leading to a limit of detection at 0.003 mg/kg. Thirteen blank shellfish homogenates were spiked with certified mussel material containing DA to levels in the range of 0.125 mg DA/kg, and analyzed in quadruplicate on 3 different days. The relative standard deviation (RSD) under intra-assay repeatability conditions ranged from 6.5 to 13.1%, and under interassay repeatability conditions the RSD ranged from 5.7 to 13.4%, with a mean value of 9.3%. The recoveries ranged from 85.5 to 106.6%, with a mean recovery of 102.2%. A method comparison was conducted with liquid chromatography with ultraviolet detection, using naturally contaminated scallop samples (n = 27) with DA levels at 0244 mg/kg. The overall correlation coefficient was 0.960 and the slope of the regression was 1.218, indicating a good agreement between the methods.


2001 ◽  
Vol 84 (5) ◽  
pp. 1643-1648 ◽  
Author(s):  
Ian Garthwaite ◽  
Kathryn M Ross ◽  
Christopher O Miles ◽  
Lyn R Briggs ◽  
Neale R Towers ◽  
...  

Abstract Enzyme-linked immunosorbent assays (ELISAs) were developed for amnesic, neurotoxic, and diarrhetic shellfish poisoning (ASP, NSP, and DSP) toxins and for yessotoxin. These assays, along with a commercially available paralytic shellfish poisoning (PSP) ELISA, were used to test the feasibility of an ELISA-based screening system. It was concluded that such a system to identify suspect shellfish samples, for subsequent analysis by methods approved by international regulatory authorities, is feasible. The assays had sufficient sensitivity and can be used on simple shellfish extracts. Alcohol extraction gave good recovery of all toxin groups. The ease of ELISAs permits the ready expansion of the system to screen for other toxins, as new ELISAs become available.


Sign in / Sign up

Export Citation Format

Share Document