Cryptosporidium spp. and cryptosporidiosis.

This article gives an overview of the application of nanomaterials in environmental remediation. In the area of environmental remediation, nanomaterials offer the potential for the efficient removal of pollutants and biological contaminants. Nanomaterials in various shapes/morphologies, such as nanoparticles, tubes, wires, fibres etc., function as adsorbents and catalysts and their composites with polymers are used for the detection and removal of gases (SO2, CO, NOx, etc.), contaminated chemicals (arsenic, iron, manganese, nitrate, heavy metals, etc.), organic pollutants (aliphatic and aromatic hydrocarbons) and biological substances, such as viruses, bacteria, parasites and antibiotics. Nanomaterials show a better performance in environmental remediation than other conventional techniques because of their high surface area (surface-to-volume ratio) and their associated high reactivity. Recent advances in the fabrication of novel nanoscale materials and processes for the treatment of drinking water and industrial waste water contaminated by toxic metal ions, radionuclides, organic and inorganic solutes, bacteria and viruses and the treatment of air are highlighted. In addition, recent advances in the application of polymer nanocomposite materials for the treatment of contaminants and the monitoring of pollutants are also discussed. Furthermore, the research trends and future prospects are briefly discussed.

A review on nanomaterials for environmental remediation

Background Small numbers of Cryptosporidium parvum oocysts can contaminate even treated drinking water, and ingestion of oocysts can cause diarrheal disease in normal as well as immunocompromised hosts. Since the number of organisms necessary to cause infection in humans is unknown, we performed a study to determine the infective dose of the parasite in healthy adults. Methods After providing informed consent, 29 healthy volunteers without evidence of previous C. parvum infection, as determined by the absence of anti-cryptosporidium–specific antibodies, were given a single dose of 30 to 1 million C. parvum oocysts obtained from a calf. They were then monitored for oocyst excretion and clinical illness for eight weeks. Household contacts were monitored for secondary spread. Results Of the 16 subjects who received an intended dose of 300 or more oocysts, 14 (88 percent) became infected. After a dose of 30 oocysts, one of five subjects (20 percent) became infected, whereas at a dose of 1000 or more oocysts, ...

https://www.nejm.org/doi/pdf/10.1056/NEJM199503303321304

The Infectivity of Cryptosporidium parvum in Healthy Volunteers

http://dbkgroup.org/Papers/davey_kell_micrev96.pdf

Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses.

Epidemiology of Cryptosporidium: transmission, detection and identification.

The survival of various isolates of Cryptosporidium parvum oocysts under a range of environmental pressures including freezing, desiccation, and water treatment processes and in physical environments commonly associated with oocysts such as feces and various water types was monitored. Oocyst viability was assessed by in vitro excystation and by a viability assay based on the exclusion or inclusion of two fluorogenic vital dyes. Although desiccation was found to be lethal, a small proportion of oocysts were able to withstand exposure to temperatures as low as -22 degrees C. The water treatment processes investigated did not affect the survival of oocysts when pH was corrected. However, contact with lime, ferric sulfate, or alum had a significant impact on oocyst survival if the pH was not corrected. Oocysts demonstrated longevity in all water types investigated, including seawater, and when in contact with feces were considered to develop an enhanced impermeability to small molecules which might increase the robustness of the oocysts when exposed to environmental pressures.

Survival of Cryptosporidium parvum oocysts under various environmental pressures.

A viability assay for oocysts of Cryptosporidium parvum based on the inclusion or exclusion of two fluorogenic vital dyes, 4',6-diamidino-2-phenylindole (DAPI) and propidium iodide, was developed by using several different isolates of oocysts. Correlation of this assay with viability measured by in vitro excystation was highly statistically significant, with a calculated correlation coefficient of 0.997. In this research, two similar excystation protocols were utilized, and no significant difference between excystation protocols was detected. Percent excystation of oocyst suspensions could be increased or reduced by inclusion of a preincubation treatment in either excystation protocol, and this alteration was also demonstrated in the viability assay. Oocysts which excluded both dyes would not excyst in vitro unless a further trigger was provided and were more resistant to acid or alkali treatment. The results of this research provide a reproducible, user-friendly assay which is applicable to individual oocysts and also provides a useful adjunct for identification of oocysts in water and environmental samples.

Viability of Cryptosporidium parvum oocysts: correlation of in vitro excystation with inclusion or exclusion of fluorogenic vital dyes.

Combination of ferric and MIEX for the treatment of a humic rich water.

Protocols for in vitro excystation of oocysts of Cryptosporidium parvum, including different chemical pre-incubation steps, were compared to examine some of the biochemical triggers involved in excystation and to define an in vitro excystation protocol of a reproducibly high efficiency. Pre-incubation steps which increased the permeability of the oocysts were found to enhance excystation dynamics and pre-treatment of oocysts with saliva was found to decrease the permeability and reduce excystation. Although excystation was maximal after incubation for 4 h, sporozoites tended to lyse over this period, and maximum sporozoite recovery occurred after 30 min. The results obtained are discussed in relation to excystation protocols adopted by different research groups and a number of recommendations are given for in vitro excystation of C. parvum oocysts.

A.T. Campbell

Papers

Survival of Cryptosporidium parvum oocysts under various environmental pressures.

Viability of Cryptosporidium parvum oocysts: correlation of in vitro excystation with inclusion or exclusion of fluorogenic vital dyes.

Combination of ferric and MIEX for the treatment of a humic rich water.

In vitro excystation of Cryptosporidium parvum.

Giardia cysts and Cryptosporidium oocysts at sewage treatment works in Scotland, UK