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1.
BMC Microbiol ; 6: 63, 2006 Jul 13.
Article in English | MEDLINE | ID: mdl-16839422

ABSTRACT

BACKGROUND: Interactions between Mycobacterium avium subsp. paratuberculosis (Map) and free-living protozoa in water are likely to occur in nature. The potential impact of ingestion of Map by two naturally occurring Acanthamoeba spp. on this pathogen's survival and chlorine resistance was investigated. RESULTS: Between 4.6 and 9.1% of spiked populations of three Map strains (NCTC 8578, B2 and ATCC 19698), which had been added at a multiplicity of infection of 10:1, were ingested by Acanthamoeba castellanii CCAP 1501/1B and A. polyphaga CCAP 1501/3B during co-culture for 3 h at 25 degrees C. Map cells were observed to be present within the vacuoles of the amoebae by acid-fast staining. During extended co-culture of Map NCTC 8578 at 25 degrees C for 24 d with both A. castellanii and A. polyphaga Map numbers did not change significantly during the first 7 days of incubation, however a 1-1.5 log10 increase in Map numbers was observed between days 7 and 24 within both Acanthamoeba spp. Ingested Map cells were shown to be more resistant to chlorine inactivation than free Map. Exposure to 2 mug/ml chlorine for 30 min resulted in a log10 reduction of 0.94 in ingested Map but a log10 reduction of 1.73 in free Map (p < 0.001). CONCLUSION: This study demonstrated that ingestion of Map by and survival and multiplication of Map within Acanthamoeba spp. is possible, and that Map cells ingested by amoebae are more resistant to inactivation by chlorine than free Map cells. These findings have implications with respect to the efficacy of chlorination applied to Map infected surface waters.


Subject(s)
Acanthamoeba castellanii/microbiology , Acanthamoeba/microbiology , Chlorine/pharmacology , Drug Resistance, Bacterial , Mycobacterium avium subsp. paratuberculosis/drug effects , Mycobacterium avium subsp. paratuberculosis/growth & development , Acanthamoeba/growth & development , Acanthamoeba castellanii/growth & development , Animals , Coculture Techniques , Microscopy, Electron , Water/parasitology , Water Microbiology
2.
Fertil Steril ; 85(3): 653-60, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16500334

ABSTRACT

OBJECTIVE: To investigate effects of delta-9-tetrahydrocannabinol (THC) on human sperm function in vitro. DESIGN: Laboratory analysis of sperm motility after exposure to THC using computer-assisted semen analysis and acrosome reaction by fluoroscein isothiocyanate-labeled peanut agglutinin staining. SETTING: An assisted reproductive technology unit. PATIENT(S): Seventy-eight male patients. INTERVENTION(S): Sperm were divided into 90% (the best fertilizing potential used in assisted conception) and 45% (the poorer subpopulation) fractions by density centrifugation and incubated with THC at concentrations equivalent to therapeutic (0.032 microM) and recreational (0.32 and 4.8 microM) plasma levels at 37 degrees C for 3 h. MAIN OUTCOME MEASURE(S): Sperm motility and spontaneous and induced acrosome reactions. RESULT(S): Percentage progressive motility was decreased dose dependently in the 90% fraction (by 2%-21%; P<.05; P<.001). The 45% fraction showed a greater decrease in percentage progressive motility (by 28% at 0.032 microM; 56% at 4.8 microM; P=.004 and P=.01 res). Straight line velocity and the average path velocity also were reduced (by 10%, in the 90% LAYER) in both fractions. Spontaneous acrosome reactions were reduced in the 90% (17% at 0.032 microM, 35% at 4.8 microM P=.004 and P<.001 resp) and more markedly in the 45% fractions (17%-35%; P<.001). When the acrosome reaction was artificially induced (90% fraction) by A23187, THC (4.8 microM) resulted in a 57% inhibition (P<.001). CONCLUSION(S): The use of THC as a recreational drug may adversely affect male fertility.


Subject(s)
Acrosome Reaction/drug effects , Cannabis/chemistry , Dronabinol/pharmacology , Sperm Motility/drug effects , Spermatozoa/drug effects , Spermatozoa/physiology , Adult , Calcimycin/pharmacology , Humans , In Vitro Techniques , Ionophores/pharmacology , Male
3.
Appl Environ Microbiol ; 71(11): 7107-12, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16269747

ABSTRACT

Mycobacterium avium subsp. paratuberculosis is the known cause of Johne's disease of both domestic and wild ruminants and has been implicated as a possible cause of Crohn's disease in humans. The organism is shed in the feces of infected animals and can survive for protracted periods in the environment and hence could be present in catchment areas receiving agricultural runoff. A limited survey was undertaken in Northern Ireland to test for M. avium subsp. paratuberculosis in untreated water entering nine water treatment works (WTWs) over a 1-year period. Three detection methods were employed, viz., immunomagnetic separation-PCR and culture on Herrold's egg yolk medium (HEYM) and BACTEC 12B medium, the latter both supplemented with mycobactins. Of the 192 untreated water samples tested, 15 (8%) tested M. avium subsp. paratuberculosis positive by one or more of the three detection methods. M. avium subsp. paratuberculosis was successfully isolated from eight untreated water samples, three by BACTEC culture and five by culture on HEYM. Although the highest incidence of M. avium subsp. paratuberculosis was found in spring, overall, there was no statistically significant difference between the seasons. No significant correlation was found between numbers of coliforms or fecal coliforms and the presence of M. avium subsp. paratuberculosis. In general, a higher incidence of M. avium subsp. paratuberculosis was found in untreated water entering those WTWs that had a high mean water pH value over the sampling period. This work indicates the need to determine the efficacy of water treatment processes to either kill or remove M. avium subsp. paratuberculosis from untreated water and the possible risks posed by contact with recreational water sources.


Subject(s)
Fresh Water/microbiology , Mycobacterium avium subsp. paratuberculosis/isolation & purification , Water Purification/methods , Water Supply , Bacteriological Techniques , Culture Media , DNA, Bacterial/analysis , Immunomagnetic Separation , Mycobacterium avium subsp. paratuberculosis/genetics , Mycobacterium avium subsp. paratuberculosis/growth & development , Northern Ireland , Polymerase Chain Reaction , Seasons
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