SILVA-NETO, I. D. da
Laboratório de Protistologia, Departamento de Zoologia, Instituto de Biologia, C.C.S., Universidade Federal do Rio de Janeiro, Ilha do Fundão, CEP 21941-590, Rio de Janeiro, RJ, Brazil
Correspondence to: Inácio Domingos da Silva-Neto, Laboratório de Protistologia, Departamento de Zoologia, Instituto de Biologia, C.C.S., Universidade Federal do Rio de Janeiro, Ilha do Fundão, CEP 21941-590, Rio de Janeiro, RJ, Brazil
The research on ciliates, flagelates and opalinates have been widespread by the utilization of techniques employing silver impregnation (Protargol), modified by several authors. However, these are time consuming and its results are variable. The present work is a variant of the technique described by Tuffrau (1964, 1967) showing some adaptations made in our laboratory. The organisms can be preserved by different fixatives (alcoholic Bouin, Stieve's fluid, 2.5% glutaraldehyde and others) and then rinsed in destilled water followed by a fast clarification by 3% sodium hypochloride. If the organism is very sensitive to hypochloride, 4% sodium lauryl sulfate may be used and then washed 3 times in distilled water. The protista can be adhered to the glass slides with Mayer's glycerinated-albumin (1 glycerin vol. to 1 or 2 albumin vol.), diluted in water at a proportion of 1:10 Cv/v., or with 1% polylysine followed by fast washes with distilled water. After the slide preparation, they were covered with a layer of 0,8% Silver proteinate. Right after that, the slide has to be placed in a glass tray lined with moist tissue and covered to prevent the proteinate to dry. The tray was placed in a incubator at 40º-50ºC for 30 minutes. The slides are rinsed for 1 minute. with warm (35ºC) distilled water. The development of the material should be done with 0.4% hydroquinone with a maximum incubation time of 1 minute. It should be developed gradually, controlling the silver impregnation intensity by observation under optical microscope. Next, rinse in distilled water for 1 minute, and then, fix in 2,5% Sodium thiosulfate. Rinse the slide for two minutes before dehydrating it in an alcoholic serial 50-100º. Finally rinse the slides in xylene. Mount the slides with Entellan MerckTM or Canada balsam.
Key words: impregnation of protists, protargol, technique improvement.
◊ A public release from Rev. Bras. Biol. vol.60 no.3 São Carlos Aug. 2000, viewed from Biology-Online.org.
The silver proteinate impregnating technique (Protargol) offers great results and many advantages among other silver-based impregnation techniques used for optical microscopy. Its results show in great detail morphological key features of ciliates, flagellates and opalinates.
Researches with protists of several environments have been increased using the protargol, which is an impregnation, not a coloration technique, whose impregnating agent is the silver proteinate. Several authors (Dieckerman, 1995; Foissner, 1991; Dragesco & Dragesco-Kernéis, 1986; Wilbert, 1975) have modified the primary technique of Bodian (1936, 1937) with the aim of obtaining satisfactory results, but these generally take a long time to develop.
The present work is a variation of the technique of protargol described by Tuffrau (1964, 1967) and was made with some modifications in the laboratory. The primordial objective was to get satisfactory results in a relatively short time and to process numerous slides with a reduced expense of silver proteinate.
The photomicrographs of the boards presented in this work were made using the technique described below. The boards show the improved structural details of the cortex and endoplasma of a flagellate, of an opalinate and of ciliates of different environments and which belong to several groups (Karyorelictea, Gymnostomatida, Prostomatida, Peniculina, Colpodida, Heterotrichida and Hypotrichida). For the identification of these organisms it is necessary to make the somatic and oral infraciliature evident, as well as the form of the macro and micronucleus. A brief comparison of the technique of protargol with other techniques that use silver salts as impregnating agent is made.
The ciliates Tracheloraphis phenicoptera, Coleps sp. and Diophrys appendiculata were collected from Baía de Guanabara, Rio de Janeiro; Lacrymaria olor and Spirostomum minus were collected in bromeliad; Colpoda cucullus was collected, in form of cysts, from the filter in the air conditioner of the laboratory. Paramecium aurelia and Euplotes woodruffi were collected from Lagoa de Piratininga in Niterói. Fabrea salina was collected from Lagoa de Araruama in Rio de Janeiro. Trichonympha sp. was isolated from digestive apparatus of termites. The opalinates were isolated from the digestive apparatus of tadpoles Physalaemus signifer.
The ciliates were cultivated in petri dishes with rice or wheat grains, except the opalinates and flagellates. The fixatives used were: 2% Osmiun tetroxide (T. phenicoptera), alcoholic-Bouin (D. appendiculata and Coleps sp.), Stieves' solution(L. olor, S. minus, C. cucullus, P. aurelia, E. woodruffi and F. salina) and 2,5% glutaraldehyde (Trichonynpha sp. and the Opalinata).
Alcoholic-Bouin: 150 ml 80% alcohol + 60 ml formaldehyde PA + 1 g of picric acid + 15 ml glacial acetic acid. This is an excellent fixative, one of its advantage is facilitating attaching the ciliates in the bottom of the clock glass, facilitating the subsequent washes.
Solution of Stieves: (modified by Foissner, 1991); 3,8 ml of aqueous mercury chloride (dissolve 30 g HgCl2 in 500 ml of hot distilled water) + 2 ml of commercial formaldehyde PA + 0,3 ml of concentrated glacial acetic acid. freshly prepared; the components can be stored.
Glycerinated-albumin of Mayer: For the preparation of the Glycerinated-Albumin of Mayer is recommended the use of two chicken eggs. Remove the albumin of the egg and filter through a nylon filter and mix 30 ml of the filtered albumin with 20 ml of glycerin; add 3 drops of formaldehyde PA to avoid the contamination of the material.
1% hydroquinone: place 2,5 g of sodium sulfite in 50 ml of distilled water, dissolve, and later add 0,5 g of hidroquinone.
1) Isolation and fixation of the specimens.
1.1) Under a stereoscopic microscope with transmitted light, the ciliates, flagellates or opalinates should be isolated and taken out from a Petri dish and transfered to a small glass recipient or a glass slide with the aid of a micropipete.
1.2) The ciliates, separated with little water, can be fixed with alcoholic Bouin, solution of Stieves or with 2,5% glutaraldehyde and 2% osmium tetroxide, for 20 minutes. The kind of fixative can vary according to the species.
1.3) Immediately after fixing, wash the specimens three times in distilled water.
2) Clarification and cleaning of the cells.
2.1) To clarify and remove fragments of organic matter attached to the cells, add in the last two washes, two or three drops of 3% sodium hipochloride. Mix and incubate for about 30 seconds, but control the clarification under the magnifying glass, to avoid the bursting of the cells and then wash three times or more. If necessary, repeat the clarification, leaving the cells less time in the hipochloride. For some more sensitive protists 4% sodium lauryl sulfate can be used for the cleaning of the cells.
2.2) After the cleaning and clarification, the cells should be distributed in degreased slides. Add on the cells a small drop of glycerinated albumin of Mayer solution (albumin of egg + glycerin in the proportion of 1:1 or 2:1 ), diluted before use with distilled water in the proportion 1:10, to avoid albumin excess in the final preparation. The material should be spread to be well homogenized and left to dry in ambient temperature, for several hours, or in incubator at 40 to 50oC. For obtaining success it is important to use the minimum of albumin to attach the cells.
The albumin dipped in the distilled water can also be placed in a small watch glass recipient, on the clarified cells, before distributing them in the slides. 1% polylysine in PBS can also be used to attach the cells on the slides. Later proceed a wash in a staining jar with distilled water and then, without drying the preparation, cover the cells with silver proteinate, as in the stage 3.
3) Impregnation and development of the specimens.
3.1) Before covering the cells with silver proteinate, cover the preparation with a mixture of alcohol-formoldehyde in the proportion of 8:2. Let it act during one minute and wash it with distilled water for two minutes. This procedure avoids the detachment of the cells during the processing of the technique.
Use a rectangular glass tray, with a lid and cover the bottom with moisten filter paper. Distribute the dry slides with the ciliates attached to them on the bottom of the tray and using a Pasteur pipette cover the preparations with drops of 0,8% or 1% silver proteinate. Place the covered tray in the incubator at 45oC-50oC, for 30 to 60 minutes, depending on the size of the protozoan. It is advisable to avoid the total evaporation of the silver proteinate of the preparation.
3.2) Remove the tray from the incubator to process the revelation of the slides, one at time. Wash the slide quickly in distilled water and quickly place it in a staining jar with 0,4% hydroquinone to reveal the preparation for 10 to 20 seconds. After brief wash in distilled water, an observation is done under the microscope to control impregnation. If necessary, it can be left more time in the developer, which can vary in concentration.
3.3) After reaching the desired impregnation, place the slide for about 30 seconds in the 2,5% sodium thiosulfate, to fix the impregnation. If the impregnation of the cells decreases, return it to the developer.
3.4) After passing it in the sodium thiosulfate, wash the slide for one minute in distilled water and begin the dehydration with alcoholic series from 50%-100% and finally in three jars with xylene.
Set up the slides covering the preparation with two drops of Entellan Merck or in diluted balsam from Canada, before placing the coverslip.
The silver impregnation technique (protargol) offers for optical microscopy the best results in the revelation of morphologic characteristics of the structures of the cortex and endoplasma, as well as the form and disposition of the nuclei of protista ciliates, flagellated and opalinates.
The silver proteinate, used in the technique, acts as an impregnanting agent, on the level of the kinetossomes or basal corpuscles of the cilia and flagellum. With the impregnation of these it is placed in evidence the distribution of the somatic kineties and organization of the cilia and flagellum of the oral area of the protozoan, facilitating the counting and description of its components.
The modifications and improvements of the protargol technique started with the results presented by Bodian (1936, 1937), who used the technique for the revelation of cells of the nervous tissue.
The modifications of the technique described by several researchers (Dieckerman, 1995; Dragesco, 1962; Foissner, 1991; Hiller, 1991; McCoy, 1974; Montagnes & Lynn, 1987; Moskowitz, 1950; Ng & Nielsen, 1977; Repak & Cribbins, 1966; Tuffrau, 1964, 1967; Wilbert, 1975; Zagon, 1970), were made for optimal results and adapted to the material available in their laboratories, thanks to a vast possibility of variation of the technique.
Tuffrau (1964, 1967) suggest that a minimum of albumin-glycerol of Mayer solution should be used to attach the cells in the slide, diluted in a proportion of 1:10, to form a very fine layer on the slide. The addition of the albumin-glycerol of Mayer on the cells can be done directly on the slide or in a small glass recipient or clock glass; in this case, after homogenization, the cells are distributed diluted in Mayer solution over several slides or coverslips. It is adequate the attachment of the cells in coverslips, to facilitate posterior observation under the microscope of both faces of the impregnated specimen.To avoid the detachment of the cells during the processing of the technique, Tuffrau (1967) suggest the immersion of the slides in the alcool-formol v/v, for 3 minutes. Foissner (1991) suggest the use of the albumin¾glycerol after a month of stability in the refrigerator. For the attachment of the cells on the slides or coverslips is adequate as an alternative, the use of polylysine. Which was not used before in the impregnation technique.
The time of impregnation of the cells may vary, as well as the temperature of the incubator.
The concentration of the hydroquinone can be from 0.4% to 1%. It is adequate a lower concentration. The preparation should be revealed first at very short times and after, the tonality of the impregnation controlled under the microscope. The recommended tonality resembles the color of Whisky. Tuffrau suggests a imersion in 5% sodium thiosulfate, if the specimens are too dark.
The fixation of the impregnation in sodium thiosulfate should be made between 30 seconds and one minute. Because this may darken the preparation, this stage is very important for the preservation of the impregnated cells for long term storage of the slides in collections.
Finally is adequate the use of the Entellan in stead of balsam from Canada for the mounting of the slides.
In addition to the technique of the protargol, other impregnation techniques by silver can be used, such as the technique of Chatton & Lwoff (1930), of Klein (1915) and of Fernando-Galeano (1976), that also offer great results in the revelation of important morphological data. But the first, which reveals most of the structures of the cortex of the cell very well, does not evidence the organelles and nuclei of endoplasma. Klein's technique, also called dry silver, does not reveal the whole structures of the cortex, but it evidences the plates of the submembranal cytoskeleton, that exist in several ciliates species. These structures are not very proeminent with protargol, that complements the study of certain protista species. The technique of Fernando-Galeano, also called the technique of the carbonate of silver amoniacal, offers great results like protargol, but it does not allow the preparation of definitive slides for storage in collections. It is necessary to underline that the results of the technique of the protargol are complements of the observation of the protozoan in vivo.
Acknowledgments — I would like to thank the trainees of the laboratory (Anderson Bruno de Matos, Flávio Joppert, Fábio Lima Custódio and Maurício Guimarães Gomes Moreira) and to Prof. Ulisses Lins of the Section of Electronic Microscopia of Inst. of Microbiology-UFRJ, for the access to the optical Microscope Axioplan II of Zeiss, in which the photomicrographs of this work were taken. The work was developed with support of the CNPq (520901/95-9), PRONEX (0877) FAPERJ (E-26/170.583/95) and CPEG-UFRJ (351905P077-8).
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