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  • 1
    In: Virus Research, Elsevier BV, Vol. 35, No. 2 ( 1995-2), p. 123-141
    Type of Medium: Online Resource
    ISSN: 0168-1702
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1995
    detail.hit.zdb_id: 1500820-4
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  • 2
    In: Journal of Clinical Microbiology, American Society for Microbiology, Vol. 58, No. 10 ( 2020-09-22)
    Abstract: Hepatitis A virus (HAV) is a common infection that is transmitted through the fecal-oral route, shed in the stool of infected individuals, and spread either by direct contact or by ingesting contaminated food or water. Each year, approximately 1.4 million acute cases are reported globally with a major risk factor for exposure being low household socioeconomic status. Recent trends show a decrease in anti-HAV antibodies in the general population, with concomitant increases in the numbers of HAV outbreaks. In line with a recreational water study, this effort aims to assess the prevalence of salivary IgG antibodies against HAV and subsequent incident infections (or immunoconversions) in visitors to a tropical beach impacted by a publicly owned treatment works (POTW). We applied a multiplex immunoassay to serially collected saliva samples gathered from study participants who recreated at Boquerón Beach, Puerto Rico. Analysis of assay results revealed an immunoprevalence rate of 16.17% for HAV with 1.43% of the cohort immunoconverting to HAV. Among those who immunoconverted, 10% reported chronic gastrointestinal symptoms and none experienced diarrhea. Tests on water samples indicated good water quality with low levels of fecal indicator bacteria; however, the collection and analysis of saliva samples afforded the ability to detect HAV infections in beachgoers. This rapid assay serves as a cost-effective tool for examining exposure to environmental pathogens and can provide critical information to policy makers, water quality experts, and risk assessment professionals seeking to improve and protect recreational water and public health.
    Type of Medium: Online Resource
    ISSN: 0095-1137 , 1098-660X
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2020
    detail.hit.zdb_id: 1498353-9
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2001
    In:  Water Research Vol. 35, No. 11 ( 2001-8), p. 2779-2783
    In: Water Research, Elsevier BV, Vol. 35, No. 11 ( 2001-8), p. 2779-2783
    Type of Medium: Online Resource
    ISSN: 0043-1354
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2001
    detail.hit.zdb_id: 202613-2
    detail.hit.zdb_id: 1501098-3
    SSG: 14
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  • 4
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1995
    In:  Canadian Journal of Microbiology Vol. 41, No. 4-5 ( 1995-04-01), p. 316-322
    In: Canadian Journal of Microbiology, Canadian Science Publishing, Vol. 41, No. 4-5 ( 1995-04-01), p. 316-322
    Abstract: We tested the ability of hollow-fiber ultrafilters with molecular weight cut-offs (MWCOs) of 50 000, 13 000, and 6000 to remove and detect viral agents (phage T1, 50–150 nm; phage PP7, poliovirus, 28–30 nm) from ultrapure water, 0.85% saline with 1% trypticase soy broth, and Dulbecco's modified Eagle minimum essential medium with 10% fetal bovine serum (DMEM-10). Virus diluted in saline and DMEM-10 were tested to evaluate filter performance under conditions that minimize the adsorption of viral particles to the filter matrix. During filtration, the retentate was returned to the input reservoir, and the permeate was removed to a separate vessel. Thus, the virus concentration in the feed increased over the course of filtration. Filter performance was evaluated by comparing the concentration of infectious virus in the initial virus suspension with the virus concentration in the permeate and retentate. Very efficient removal of phages T1 and PP7 was observed with the filters with MWCOs of 13 000 and 6000 (titer reduction 〉  7 logs) for all three fluids tested. No poliovirus was detected in the permeate of the ultrafilters with MWCOs of 13 000 or 6000 (titer reduction 〉  6 logs). These results indicate that the ultrafilters with MWCOs of 13 000 and 6000 were very effective in removing small viral particles (25–30 nm) by size exclusion. The recovery efficiency of the virus in the retentate varied by fluid type. However, filtration with virus diluted in DMEM-10 resulted in consistent recovery of the viruses tested. The results suggest that these ultrafilters may have the dual potential of removing viral contaminants from fluids and concentrating virus in the retentate.Key words: virus removal, virus concentration, ultrafiltration membranes.
    Type of Medium: Online Resource
    ISSN: 0008-4166 , 1480-3275
    RVK:
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1995
    detail.hit.zdb_id: 280534-0
    detail.hit.zdb_id: 1481972-7
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2008
    In:  Journal of Environmental Monitoring Vol. 10, No. 6 ( 2008), p. 718-
    In: Journal of Environmental Monitoring, Royal Society of Chemistry (RSC), Vol. 10, No. 6 ( 2008), p. 718-
    Type of Medium: Online Resource
    ISSN: 1464-0325 , 1464-0333
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2008
    detail.hit.zdb_id: 2027542-0
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  • 6
    In: Environmental Science & Technology, American Chemical Society (ACS), Vol. 46, No. 2 ( 2012-01-17), p. 945-953
    Type of Medium: Online Resource
    ISSN: 0013-936X , 1520-5851
    RVK:
    Language: English
    Publisher: American Chemical Society (ACS)
    Publication Date: 2012
    detail.hit.zdb_id: 280653-8
    detail.hit.zdb_id: 1465132-4
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  • 7
    Online Resource
    Online Resource
    The American Association of Immunologists ; 2020
    In:  The Journal of Immunology Vol. 204, No. 1_Supplement ( 2020-05-01), p. 86.38-86.38
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 204, No. 1_Supplement ( 2020-05-01), p. 86.38-86.38
    Abstract: Understanding and curbing the mounting global increase in waterborne pathogen outbreaks are quickly becoming major priorities for public health professionals and policy makers. According to the World Health Organization (WHO), 60% of global diarrheal deaths are caused by unsafe water and lack of sanitation or hygiene. The WHO estimates that at least 2 billion people use a drinking water source contaminated with feces. Contaminated water -- shown to transmit diseases such as cholera, dysentery, typhoid, hepatitis A, and polio -- is estimated to cause almost half a million diarrheal deaths each year. The United States Environmental Protection Agency has prioritized efforts to understand the links between water quality and human health effects. To that end, we have developed and applied a salivary-IgG antibody multiplex immunoassay to measure human exposures and associated health effects to multiple pathogens simultaneously. Saliva is emerging as a cost-effective, noninvasive biofluid that is well-accepted by children. The multiplex immunoassay has afforded the ability to assess immunopositivity, immunoprevalence, co-infections and incident infections (immunoconversions) to Helicobacter pylori, Campylobacter jejuni, Cryptosporidium parvum, Toxoplasma gondii, hepatitis A virus and noroviruses GI.I and GII.4 at several beaches throughout the US. Further, we’ve found evidence of asymptomatic norovirus and hepatitis A infections in visitors to a fecally contaminated beach. The assay produces results in as little as one hour and when used in conjunction with epidemiologic and water quality studies, provides valuable information that links human health effects more directly to water quality.
    Type of Medium: Online Resource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Language: English
    Publisher: The American Association of Immunologists
    Publication Date: 2020
    detail.hit.zdb_id: 1475085-5
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  • 8
    Online Resource
    Online Resource
    American Society for Microbiology ; 2002
    In:  Applied and Environmental Microbiology Vol. 68, No. 1 ( 2002-01), p. 161-165
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 68, No. 1 ( 2002-01), p. 161-165
    Abstract: Fecal samples were taken from wild ducks on the lower Rio Grande River around Las Cruces, N. Mex., from September 2000 to January 2001. Giardia cysts and Cryptosporidium oocysts were purified from 69 samples by sucrose enrichment followed by cesium chloride (CsCl) gradient centrifugation and were viewed via fluorescent-antibody (FA) staining. For some samples, recovered cysts and oocysts were further screened via PCR to determine the presence of Giardia lamblia and Crytosporidium parvum . The results of this study indicate that 49% of the ducks were carriers of Cryptosporidium , and the Cryptosporidium oocyst concentrations ranged from 0 to 2,182 oocysts per g of feces (mean ± standard deviation, 47.53 ± 270.3 oocysts per g); also, 28% of the ducks were positive for Giardia , and the Giardia cyst concentrations ranged from 0 to 29,293 cysts per g of feces (mean ± standard deviation, 436 ± 3,525.4 cysts per g). Of the 69 samples, only 14 had (oo)cyst concentrations that were above the PCR detection limit. Samples did test positive for Cryptosporidium sp. However, C. parvum and G. lamblia were not detected in any of the 14 samples tested by PCR. Ducks on their southern migration through southern New Mexico were positive for Cryptosporidium and Giardia as determined by FA staining, but C. parvum and G. lamblia were not detected.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2002
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    American Society for Microbiology ; 2002
    In:  Applied and Environmental Microbiology Vol. 68, No. 3 ( 2002-03), p. 1115-1121
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 68, No. 3 ( 2002-03), p. 1115-1121
    Abstract: Microscopic detection of Cryptosporidium parvum oocysts is time-consuming, requires trained analysts, and is frequently subject to significant human errors. Artificial neural networks (ANN) were developed to help identify immunofluorescently labeled C. parvum oocysts. A total of 525 digitized images of immunofluorescently labeled oocysts, fluorescent microspheres, and other miscellaneous nonoocyst images were employed in the training of the ANN. The images were cropped to a 36- by 36-pixel image, and the cropped images were placed into two categories, oocyst and nonoocyst images. The images were converted to grayscale and processed into a histogram of gray color pixel intensity. Commercially available software was used to develop and train the ANN. The networks were optimized by varying the number of training images, number of hidden neurons, and a combination of these two parameters. The network performance was then evaluated using a set of 362 unique testing images which the network had never “seen” before. Under optimized conditions, the correct identification of authentic oocyst images ranged from 81 to 97%, and the correct identification of nonoocyst images ranged from 78 to 82%, depending on the type of fluorescent antibody that was employed. The results indicate that the ANN developed were able to generalize the training images and subsequently discern previously unseen oocyst images efficiently and reproducibly. Thus, ANN can be used to reduce human errors associated with the microscopic detection of Cryptosporidium oocysts.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2002
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
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  • 10
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 69, No. 7 ( 2003-07), p. 4098-4102
    Abstract: The detection and identification of pathogens from water samples remain challenging due to variations in recovery rates and the cost of procedures. Ultrafiltration offers the possibility to concentrate viral, bacterial, and protozoan organisms in a single process by using size-exclusion-based filtration. In this study, two hollow-fiber ultrafilters with 50,000-molecular-weight cutoffs were evaluated to concentrate microorganisms from 2- and 10-liter water samples. When known quantities (10 5 to 10 6 CFU/liter) of two species of enteric bacteria were introduced and concentrated from 2 liters of sterile water, the addition of 0.1% Tween 80 increased Escherichia coli strain K-12 recoveries from 70 to 84% and Salmonella enterica serovar Enteritidis recoveries from 36 to 72%. An E. coli antibiotic-resistant strain, XL1-Blue, was recovered at a level (87%) similar to that for strain K-12 (96%) from 10 liters of sterile water. When E. coli XL1-Blue was introduced into 10 liters of nonsterile Rio Grande water with higher turbidity levels (23 to 29 nephelometric turbidity units) at two inoculum levels (9 × 10 5 and 2.4 × 10 3 per liter), the recovery efficiencies were 89 and 92%, respectively. The simultaneous addition of E. coli XL1-Blue (9 × 10 5 CFU/liter), Cryptosporidium parvum oocysts (10 oocysts/liter), phage T1 (10 5 PFU/liter), and phage PP7 (10 5 PFU/liter) to 10 liters of Rio Grande surface water resulted in mean recoveries of 96, 54, 59, and 46%, respectively. Using a variety of surface waters from around the United States, we obtained recovery efficiencies for bacteria and viruses that were similar to those observed with the Rio Grande samples, but recovery of Cryptosporidium oocysts was decreased, averaging 32% (the site of collection of these samples had previously been identified as problematic for oocyst recovery). Results indicate that the use of ultrafiltration for simultaneous recovery of bacterial, viral, and protozoan pathogens from variable surface waters is ready for field deployment.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2003
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
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