ABSTRACT
BACKGROUND: The protozoan parasites Cryptosporidium spp. and Giardia are known to occur widely in both raw and drinking waters. They are two of the causative agents of waterborne outbreaks of gastroenteritis throughout the world. In the present study, a PCR assay and FA were developed for detection of Cryptosporidium oocysts and Giardia cyst in environmental samples. METHODS: We have detected Cryptosporidium spp. oocysts and Giardia cysts in seeded and unseeded environmental water samples by PCR method. Water samples were spiked with oocysts (50, 100,300,500) and filtrated with a 1.2-µm pore size cellulose nitrate and follow by DNA extraction and purification by QIAamp DNA mini kit. Nested-PCR assay amplified an 850 bp fragment of 18s rRNA gene specific for Cryptosporidium and 435 bp fragment of glutamate dehydrogenase (GDH) target gene for Giardia. Also many river water from north of Iran, be checked by these methods. RESULTS: Cryptosporidium and Giardia DNAs were detected in seeded water sample and Giardia was detected in all 5 water samples from river in north of Iran by nested- PCR and FA. Also in one river water sample, Cryptosporidium was detected. CONCLUSION: This protocol is effective for detection of these waterborne parasites in treated and untreated water samples. This study can also serve as a platform for further investigations and research water source in Iran.
ABSTRACT
Distribution of Mucilage Cells (MC) in leaves and petals of two species of Malva L. : Malva neglecta Wallr and M. nicaeensis All, one species of Altheae L.: A. officinalis L. and one species of Alcea L: A. angulata (Freyn and Sint.) Freyn and Sint. ex Iljin, have studied. Except ofA. angulata that mucilage cells observed both in epidermis and mesophyll of leaves, in the others mucilage cells confined to epidermis cells. All of species have mucilage cells in the petals. The area of the mucilaginous elements in the leaves and petals of species determined planimetrically on definite cross-sections was studied as a comparative element to the mucilage content determined by extracting the raw mucilage by Hot Extraction Method (HEM) and then by comparing the dry weight, comparison between species was done. A correlation between the greater area of the mucilaginous elements and the mucilage content measured by methods mentioned was shown, basing on different microscopic examination of cross-sections of the organs fixed and stained with ruthenium red. The results were shown that mucilage content in the leaves of Malva neglecta was more than the others and mucilage content in petals of Malva neglecta was more than the others.
