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1.
Cells ; 12(8)2023 04 07.
Article in English | MEDLINE | ID: mdl-37190012

ABSTRACT

CRISPR-Cas technology has rapidly changed life science research and human medicine. The ability to add, remove, or edit human DNA sequences has transformative potential for treating congenital and acquired human diseases. The timely maturation of the cell and gene therapy ecosystem and its seamless integration with CRISPR-Cas technologies has enabled the development of therapies that could potentially cure not only monogenic diseases such as sickle cell anemia and muscular dystrophy, but also complex heterogenous diseases such as cancer and diabetes. Here, we review the current landscape of clinical trials involving the use of various CRISPR-Cas systems as therapeutics for human diseases, discuss challenges, and explore new CRISPR-Cas-based tools such as base editing, prime editing, CRISPR-based transcriptional regulation, CRISPR-based epigenome editing, and RNA editing, each promising new functionality and broadening therapeutic potential. Finally, we discuss how the CRISPR-Cas system is being used to understand the biology of human diseases through the generation of large animal disease models used for preclinical testing of emerging therapeutics.


Subject(s)
CRISPR-Cas Systems , Gene Editing , Animals , Humans , CRISPR-Cas Systems/genetics , Ecosystem , Genetic Therapy , Epigenome
2.
Int J Environ Res Public Health ; 12(7): 7118-32, 2015 Jun 24.
Article in English | MEDLINE | ID: mdl-26114244

ABSTRACT

Large sample volumes are traditionally required for the analysis of waterborne pathogens. The need for large volumes greatly limits the number of samples that can be processed. The aims of this study were to compare extraction and detection procedures for quantifying protozoan parasites and viruses from small volumes of marine water. The intent was to evaluate a logistically simpler method of sample collection and processing that would facilitate direct pathogen measures as part of routine monitoring programs. Samples were collected simultaneously using a bilayer device with protozoa capture by size (top filter) and viruses capture by charge (bottom filter). Protozoan detection technologies utilized for recovery of Cryptosporidium spp. and Giardia spp. were qPCR and the more traditional immunomagnetic separation-IFA-microscopy, while virus (poliovirus) detection was based upon qPCR versus plaque assay. Filters were eluted using reagents consistent with the downstream detection technologies. Results showed higher mean recoveries using traditional detection methods over qPCR for Cryptosporidium (91% vs. 45%) and poliovirus (67% vs. 55%) whereas for Giardia the qPCR-based methods were characterized by higher mean recoveries (41% vs. 28%). Overall mean recoveries are considered high for all detection technologies. Results suggest that simultaneous filtration may be suitable for isolating different classes of pathogens from small marine water volumes. More research is needed to evaluate the suitability of this method for detecting pathogens at low ambient concentration levels.


Subject(s)
Cryptosporidium/isolation & purification , Giardia/isolation & purification , Poliovirus/isolation & purification , Seawater/microbiology , Water Microbiology , Water Quality , Filtration/methods , Immunomagnetic Separation , Polymerase Chain Reaction , Seawater/parasitology
3.
Int J Environ Health Res ; 23(1): 46-57, 2013.
Article in English | MEDLINE | ID: mdl-22924435

ABSTRACT

While the value of Staphylococcus aureus as an indicator for non-enteric diseases is unclear, understanding its prevalence in recreational beaches would prove useful, given its pathogenic potential. Staphylococcus aureus levels were evaluated in sand and seawater at three beaches during one year. To elucidate possible S. aureus sources or colonization trends, distribution in sand was analyzed at Hollywood Beach. Staphylococcus aureus levels fluctuated throughout the study with highest average densities detected in dry sand (3.46 × 105 CFU/g, Hobie Beach), particularly at beaches with high human density. Patchy distribution marked hotspots of human use and/or possible bacterial re-growth. Data from a brief epidemiological survey indicated a very slight association between beach usage and skin conditions; suggesting high S. aureus levels in sand may not necessarily constitute major health risks. Because the possibility of disease transmission exists, particularly to children and immuno-compromised beach-goers, periodic surveying of highly frequented beaches seems warranted.


Subject(s)
Bathing Beaches/standards , Geologic Sediments/microbiology , Seawater/microbiology , Skin Diseases/epidemiology , Staphylococcal Infections/epidemiology , Staphylococcus aureus/isolation & purification , Colony Count, Microbial , Environmental Monitoring , Florida/epidemiology , Geologic Sediments/chemistry , Health Status , Humans , Silicon Dioxide/chemistry , Skin Diseases/microbiology , Staphylococcal Infections/microbiology , Water
4.
J Water Health ; 9(3): 443-57, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21976192

ABSTRACT

Studies evaluating the relationship between microbes and human health at non-point source beaches are necessary for establishing criteria which would protect public health while minimizing economic burdens. The objective of this study was to evaluate water quality and daily cumulative health effects (gastrointestinal, skin, and respiratory illnesses) for bathers at a non-point source subtropical marine recreational beach in order to better understand the inter-relationships between these factors and hence improve monitoring and pollution prevention techniques. Daily composite samples were collected, during the Oceans and Human Health Beach Exposure Assessment and Characterization Health Epidemiologic Study conducted in Miami (Florida, USA) at a non-point source beach, and analyzed for several pathogens, microbial source tracking markers, indicator microbes, and environmental parameters. Analysis demonstrated that rainfall and tide were more influential, when compared to other environmental factors and source tracking markers, in determining the presence of both indicator microbes and pathogens. Antecedent rainfall and F+ coliphage detection in water should be further assessed to confirm their possible association with skin and gastrointestinal (GI) illness outcomes, respectively. The results of this research illustrate the potential complexity of beach systems characterized by non-point sources, and how more novel and comprehensive approaches are needed to assess beach water quality for the purpose of protecting bather health.


Subject(s)
Bathing Beaches , Gastrointestinal Diseases/microbiology , Respiratory Tract Infections/microbiology , Seawater/microbiology , Water Microbiology , Coliphages/isolation & purification , Enterococcus/isolation & purification , Enterovirus/isolation & purification , Environmental Exposure/adverse effects , Environmental Monitoring/methods , Epidemiological Monitoring , Florida/epidemiology , Gastrointestinal Diseases/epidemiology , Humans , Rain , Respiratory Tract Infections/epidemiology , Respiratory Tract Infections/transmission
5.
Appl Environ Microbiol ; 76(3): 724-32, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19966020

ABSTRACT

Swimming in ocean water, including ocean water at beaches not impacted by known point sources of pollution, is an increasing health concern. This study was an initial evaluation of the presence of indicator microbes and pathogens and the association among the indicator microbes, pathogens, and environmental conditions at a subtropical, recreational marine beach in south Florida impacted by non-point sources of pollution. Twelve water and eight sand samples were collected during four sampling events at high or low tide under elevated or reduced solar insolation conditions. The analyses performed included analyses of fecal indicator bacteria (FIB) (fecal coliforms, Escherichia coli, enterococci, and Clostridium perfringens), human-associated microbial source tracking (MST) markers (human polyomaviruses [HPyVs] and Enterococcus faecium esp gene), and pathogens (Vibrio vulnificus, Staphylococcus aureus, enterovirus, norovirus, hepatitis A virus, Cryptosporidium spp., and Giardia spp.). The enterococcus concentrations in water and sand determined by quantitative PCR were greater than the concentrations determined by membrane filtration measurement. The FIB concentrations in water were below the recreational water quality standards for three of the four sampling events, when pathogens and MST markers were also generally undetectable. The FIB levels exceeded regulatory guidelines during one event, and this was accompanied by detection of HPyVs and pathogens, including detection of the autochthonous bacterium V. vulnificus in sand and water, detection of the allochthonous protozoans Giardia spp. in water, and detection of Cryptosporidium spp. in sand samples. The elevated microbial levels were detected at high tide and under low-solar-insolation conditions. Additional sampling should be conducted to further explore the relationships between tidal and solar insolation conditions and between indicator microbes and pathogens in subtropical recreational marine waters impacted by non-point source pollution.


Subject(s)
Bacteria/isolation & purification , Bathing Beaches , Parasites/isolation & purification , Seawater/microbiology , Viruses/isolation & purification , Water Microbiology , Animals , Bathing Beaches/standards , Clostridium perfringens/isolation & purification , Cryptosporidium/isolation & purification , Enterococcus/isolation & purification , Enterococcus faecium/isolation & purification , Environmental Monitoring , Environmental Pollutants/isolation & purification , Escherichia coli/isolation & purification , Florida , Fresh Water/microbiology , Humans , Polyomavirus/isolation & purification , Recreation , Seawater/parasitology , Seawater/virology , Silicon Dioxide , Viruses/genetics , Water Supply
6.
Mar Pollut Bull ; 54(9): 1472-82, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17610908

ABSTRACT

Fecal indicator levels in nearshore waters of South Florida are routinely monitored to assess microbial contamination at recreational beaches. However, samples of sand from the surf zone and upper beach are not monitored which is surprising since sand may accumulate and harbor fecal-derived organisms. This study examined the prevalence of fecal indicator organisms in tidally-affected beach sand and in upper beach sand and compared these counts to levels in the water. Since indicator organisms were statistically elevated in sand relative to water, the study also considered the potential health risks associated with beach use and exposure to sand. Fecal coliforms, Escherichia coli, enterococci, somatic coliphages, and F(+)-specific coliphages were enumerated from sand and water at three South Florida beaches (Ft. Lauderdale Beach, Hollywood Beach, and Hobie Beach) over a 2-year period. Bacteria were consistently more concentrated in 100g samples of beach sand (2-23 fold in wet sand and 30-460 fold in dry sand) compared to 100ml samples of water. Somatic coliphages were commonly recovered from both sand and water while F(+)-specific coliphages were less commonly detected. Seeding experiments revealed that a single specimen of gull feces significantly influenced enterococci levels in some 3.1m(2) of beach sand. Examination of beach sand on a micro-spatial scale demonstrated that the variation in enterococci density over short distances was considerable. Results of multiple linear regression analysis showed that the physical and chemical parameters monitored in this study could only minimally account for the variation observed in indicator densities. A pilot epidemiological study was conducted to examine whether the length of exposure to beach water and sand could be correlated with health risk. Logistic regression analysis results provided preliminary evidence that time spent in the wet sand and time spent in the water were associated with a dose-dependent increase in gastrointestinal illness.


Subject(s)
Bathing Beaches , Coliphages/isolation & purification , Enterobacteriaceae/isolation & purification , Enterococcus/isolation & purification , Environmental Pollutants/isolation & purification , Gastroenteritis/epidemiology , Silicon Dioxide , Animals , Charadriiformes , Colony Count, Microbial , Environmental Exposure/adverse effects , Environmental Monitoring , Environmental Pollutants/toxicity , Epidemiological Monitoring , Feces/microbiology , Florida/epidemiology , Gastroenteritis/etiology , Humans , Seawater/microbiology , Surveys and Questionnaires
7.
Mol Microbiol ; 65(1): 64-75, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17581121

ABSTRACT

Knockout mutants of Plasmodium falciparum lacking pfpm1, pfpm2 and pfhap (triple-PM KO), and mutants lacking all four digestive vacuole (DV) plasmepsins (pfpm4, pfpm1, pfpm2 and pfhap; quadruple-PM KO), were prepared by double cross-over integration effecting chromosomal deletions of up to 14.6 kb. The triple-PM KO was similar to the parental line (3D7) in growth rate, morphology and sensitivity to proteinase inhibitors. The quadruple-PM KO showed a significantly slower rate of growth in standard medium, which manifested as delayed schizont maturation accompanied by reduced formation of haemozoin. In amino acid-limited medium, the reduction in growth rate of the quadruple-PM KO was pronounced. The sensitivity of both the triple- and quadruple-PM KOs to six different HIV aspartic proteinase inhibitors was comparable to that of 3D7, thus establishing that the DV plasmepsins were not the primary targets of the antimalarial activity of these clinically important compounds. Electron microscopic analysis revealed the presence of multilamellar bodies resembling ceroid in the DV of the quadruple-PM KO, and intermediates of the autophagic pathway accumulated as determined by Western blot analysis. Thus, the DV plasmepsins, although not essential, contribute significantly to the fitness of the parasite and are required for efficient degradation of endosomal vesicles delivered to the DV.


Subject(s)
Aspartic Acid Endopeptidases/metabolism , Plasmodium falciparum/enzymology , Vacuoles/enzymology , Animals , Antimalarials/pharmacology , Aspartic Acid Endopeptidases/antagonists & inhibitors , Aspartic Acid Endopeptidases/genetics , Erythrocytes/metabolism , Erythrocytes/parasitology , Gene Deletion , HIV Protease Inhibitors/pharmacology , Microscopy, Electron , Parasitic Sensitivity Tests , Plasmodium falciparum/drug effects , Plasmodium falciparum/genetics , Plasmodium falciparum/growth & development , Plasmodium falciparum/ultrastructure , Protozoan Proteins/antagonists & inhibitors , Protozoan Proteins/genetics , Protozoan Proteins/metabolism , Vacuoles/metabolism
8.
Int J Parasitol ; 37(3-4): 317-27, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17207486

ABSTRACT

Four of the plasmepsins of Plasmodium falciparum are localised in the digestive vacuole (DV) of the asexual blood stage parasite (PfPM1, PfPM2, PfPM4 and PfHAP), and each of these aspartic proteinases has been successfully targeted by gene disruption. This study describes further characterisation of the single-plasmepsin knockout mutants, and the creation and characterisation of double-plasmepsin knockout mutants lacking complete copies of pfpm2 and pfpm1 or pfhap and pfpm2. Double-plasmepsin knockout mutants were created by transfecting pre-existing knockout mutants with a second plasmid knockout construct. PCR and Southern blot analysis demonstrate the integration of a large concatamer of each plasmid construct into the targeted gene. All mutants have been characterised to assess the involvement of the DV plasmepsins in sustaining growth during the asexual blood stage. Analyses reaffirmed that knockout mutants Deltapfpm1 and Deltapfpm4 had lower replication rates in the asexual erythrocytic stage than the parental line (Dd2), but double-plasmepsin knockout mutants lacking intact copies of either pfpm2 and pfpm1, or pfpm2 and pfhap, had normal growth rates compared with Dd2. The amount of crystalline hemozoin produced per parasite during the asexual cycle was measured in each single-plasmepsin knockout to estimate the effect of each DV plasmepsin on hemoglobin digestion. Only Deltapfpm4 had a statistically significant reduction in hemozoin accumulation, indicating that hemoglobin digestion was impaired in this mutant. In the single-plasmepsin knockouts, no statistically significant differences were found in the steady state levels of mRNA from the remaining intact DV plasmepsin genes. Disruption of a DV plasmepsin gene does not affect the accumulation of mRNA encoding the remaining paralogous plasmepsins, and Western blot analysis confirmed that the accumulation of the paralogous plasmepsins in each knockout mutant was similar among all clones examined.


Subject(s)
Aspartic Acid Endopeptidases/genetics , Hemoglobins/metabolism , Plasmodium falciparum/genetics , Animals , Aspartic Acid Endopeptidases/physiology , Blotting, Southern/methods , Blotting, Western/methods , Erythrocytes/parasitology , Gene Deletion , Gene Expression Regulation , Genes, Protozoan , Hemeproteins/metabolism , Life Cycle Stages , Plasmodium falciparum/growth & development , Plasmodium falciparum/metabolism , Reverse Transcriptase Polymerase Chain Reaction/methods , Transfection
10.
Mutat Res ; 572(1-2): 84-97, 2005 May 02.
Article in English | MEDLINE | ID: mdl-15790492

ABSTRACT

Dequalinium (DEQ), a drug with both antimicrobial and anticancer activity, induced the formation of petite (respiration-deficient) mutants in the yeast Saccharomyces cerevisiae. DEQ was found to be approximately 50-fold more potent than ethidium bromide (EB) at inducing petites. Analysis of the DEQ-induced petite mutants indicated a complete loss of mitochondrial DNA (<1 copy/cell). Prior to the loss of mtDNA, DEQ caused cleavage of the mtDNA into a population of fragments 30-40kbp in size suggesting that this drug causes petites by inducing a breakdown of mtDNA. The selective effect of DEQ on yeast mtDNA may underlie the antifungal activity of this chemotherapeutic agent.


Subject(s)
Antineoplastic Agents/toxicity , Dequalinium/toxicity , Mutation , Saccharomyces cerevisiae/drug effects , DNA Probes , DNA, Mitochondrial/drug effects , Electrophoresis, Gel, Pulsed-Field , Ethidium/pharmacology , Microscopy, Fluorescence , Saccharomyces cerevisiae/genetics
11.
J Eukaryot Microbiol ; 51(2): 192-200, 2004.
Article in English | MEDLINE | ID: mdl-15134255

ABSTRACT

Previous molecular examination of Acanthamoeba spp. has resulted in the determination of distinct genotypes in this genus (designated T1-T12, T14). Genotype T4 has been responsible for the majority of cases of Acanthamoeba keratitis. Here we examine the relative abundance of environmental T4 isolates on beaches and ask whether they have temperature and salinity tolerances that could enhance pathogenicity. Twenty-four Acanthamoeba strains were isolated from beach sand (n = 20), soil (n = 3), and tap water (n = 1) in south Florida. Phylogenetic analysis identified 19 of 24 isolates as T4, the Acanthamoeba keratitis-associated genotype. The remaining isolates were genotype T5 (4) and T11 (1). Nearly all beach isolates were genotype T4, whereas the tap water and soil isolates were mostly T5. All amoebae grew at 0, 1.0, and 2.0% salt and 19 of 20 beach isolates also grew at 3.2%. No soil or tap-water acanthamoebae reproduced at 3.2%. All isolates grew at 37 degrees C and two (T5) at 42 degrees C. Little correlation existed between beach location, salt-tolerance, and genetic relatedness. Overall, the large majority of environmental isolates obtained were genotype T4, suggesting it may be the most common genotype in this environment and could be a potential source of Acanthamoeba keratitis infections.


Subject(s)
Acanthamoeba Keratitis/parasitology , Acanthamoeba/isolation & purification , Acanthamoeba/physiology , Acanthamoeba/genetics , Acanthamoeba/pathogenicity , Animals , Bathing Beaches , DNA, Protozoan/chemistry , DNA, Protozoan/isolation & purification , DNA, Ribosomal/chemistry , DNA, Ribosomal/isolation & purification , Florida , Fresh Water/parasitology , Genes, rRNA , Genotype , Molecular Sequence Data , Phylogeny , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA , Sodium Chloride , Temperature
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