in vitro culture and isoenzyme analysis of giardia lamblia

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(4) 0.2 and 0.3M Tris maleate buffers were prepared similarly, with the appropriate adjustments in quantities. (5) 0.3 M Tris Buffer 37.34g/L Tris buffer (Associated Chemical Enterprises cc., Reuven, SA.) (6) O,3M Tris-Hydrochloride buffer, pH adjusted to 8,0 with 10M NaOH (7) O,3M Tris-Hydrochloride buffer, pH 7,4 (8) 0,1 M Sodium di-Hydrogen phosphate, pH adjusted to 7,0 with di-Sodium Hydrogen phosphate (9) O,2M Sodium hydrogen phosphate / O,03M Boric Acid (10) O,5M Tris Hydrochloride pH adjusted to 8.0 with 10M NaOH. (11) L-Aspartic acid (30mM) is dissolved in 0.1 M Tris/HCI buffer and pH adjusted to 8.0 with KOH (12) 2-0xoglutaric acid (15mM) is dissolved in 0.1M Tris/Hel buffer and pH adjusted to 8.0 with KOH (13) 0, 2M Citrate buffer, pH 7,0 187
Appendix 10. Quantitative description of substrates, cofactors and activatiors of each enzyme system. 0.3M Tris-Hydrochloride pH7.4 14mls 14mls 0.3M Tris Hydrochloride pHS.O 14mls 14mls 14mll 14mls 3Smls NADP (10 m/gml) 1ml 1ml 1.Sml 1ml 1ml 1ml 1 M Magnesium Chloride O.4ml O.4ml O.Sml O.4ml O.Sml O.Sml G6PD (140 u/ml) O.Sml 0.2ml 0.2ml Fructose6-Phosphate(Na3 salt) 0.2ml 1M Maleate 0.4ml Glucose-1 Phoshate(Na2 salt) 2Smg Glucose ATP (Na2 salt) 20mg 40mg G6P(0.6mM )Na2 salt 10mg 6PhosphogluconateO,SmM (Na3 ) 10mg L-Aspartic aCid(30mM) 2-0xoglutaric acid (1SmM) Fast-blue 7,Sml 7.Sml 2S0mg *MTT( O.OSg/ml) 1ml 1ml 1ml 1ml 1ml 1ml tPMS (0.01g/ml) 1ml 1ml 1ml 1ml 1ml Agar (1.2%) 10ml 10ml 10ml 10ml 10ml 10ml 10ml *3-( 4,5Dimethylthiazolyl-2)-2,5 · diphenyltetrazolium Bromide (MTT) t Phenazinemethosulphate (PMS) 188
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IN VITRO CULTURE AND ISOENZYME ANAL
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(j)edicated to my {ate parents :No
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the positive specimens by sucrose g
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Declaration This study represents o
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ACKNOWLEDGEMENTS The author wishes
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Table of Contents Page CHAPTER 1 -
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4.2.1. Animal Sourcing and Care ...
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APPENDIX 8 List of enzyme systems u
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List of Tables Page Table 1.1 Commo
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List of Plates Page Plate 2.1 An eo
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ABBREVIATIONS AND UNITS OF MEASUREM
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agi/is in 1882. In 1914, Alexeieff
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unique about Giardia in humans, whi
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To-date, use of the different speci
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Differentiation into the cyst stage
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1.3 Transmission 1.3.1 Human hosts
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Owen, 1984) 1.3. 2 The Zoonosis of
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1.4 Distribution The morbidity and
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children by Schutte et al. in 1981
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of (a) the enormous absorptive capa
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Ig M (100% of patients), IgG (70%),
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chymotrypsin) between different iso
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impact on the physical growth of 29
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Figure 1.3. Transmission Electron m
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among children between the ages of
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where immunocompromised mice have p
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up to 4 distinct genotypes within e
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in initiation of infection (excysta
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In order to address these and many
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multiple stool examinations in 4 of
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2.2 MATERIALS AND METHODS 2.2.1 Spe
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Table 2.1. Semi-quantitative assess
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2.2.3.2 The modified Zinc sulphate
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Preliminary work with five samples
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% Viability = unstained cysts/total
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Table 2.3. Prevalence of Giardia in
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Table 2. 4. Monthly summary of stoo
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spp (59%). Other parasites less fre
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Observations • A large proportion
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Plate 2.1. An eosin-stained prepara
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2.4 DISCUSSION In terms of yield, i
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examination of wet preparations. Th
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ecognised (on unstained preparation
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cultivation in vitro (Kasprzak & Ma
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3.2 MATERIALS AND METHODS Three exc
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3.2.3 The modified Acid Pepsin meth
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• After 15 minutes incubation: Ma
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Plate 3.2 (b) A completely excysted
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Twenty-four batches of cysts (71 %
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3.3.3 The modified Acid Pepsin excy
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3.4 DISCUSSION Since our source of
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an unreliable indicator of viabilit
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propagating Giardia for subsequent
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4.2 MATERIALS AND METHODS 4.2.1. An
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A litter comprising of 7 C57BU6 mic
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for attached trophozoites and maint
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days pi. However, accurate quantifi
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Table 4.4. Summary of the inoculati
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not be infected in comparison with
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A proportionately higher percentage
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These findings strongly suggest tha
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CHAPTERS IN VITRO CULTURE OF GIARDI
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Diamond et al.'s (1978) medium. He
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Majewska, 1985) United States (Nash
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were evaluated. 5,2,1,2 Biosate Bio
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Table 5.1 Outlines a relative semi-
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dislodged by chilling the culture t
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Table 5.2. Sensitivity to Ciproflox
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Table 5.3. Summary results of in vi
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Once established in culture for a l
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Plates 5.3 and 5.4 Confluent growth
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difficult to produce viable culture
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dominance of certain genotypes unde
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Cryopreservation and successful ret
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adjusted to 5°C per minute from am
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6.3 RESULTS Trophozoites have been
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Table 6.1. A longevity record of sa
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Diamond (1995) stated that an impor
Page 157 and 158: into two categories. One group cont
Page 159 and 160: technique to the first local (South
Page 161 and 162: for Giardia Iysates. These included
Page 163 and 164: 4. To exclude the presence of bacte
Page 165 and 166: Plate 7.1 Banding pattern of 8 seri
Page 167 and 168: PGM activity was displayed by Giard
Page 169 and 170: Plate 7.6. Hexokinase Lane 1. Unino
Page 171 and 172: Plate 7.8. Phosphogluconate dehydro
Page 173 and 174: stably expressed between different
Page 175 and 176: techniques, which would allow diffe
Page 177 and 178: Belosevic M, Faubert GM, MacLean JD
Page 179 and 180: Farthing MJG, Mata L, Urrutia JJ, K
Page 181 and 182: Heidelberg pp.397-398. Hiatt RA, Ma
Page 183 and 184: patients with X-linked agammaglobul
Page 185 and 186: Press, Calgary. pp 57-58. Nash TE,
Page 187 and 188: of Entamoeba histolytica in a group
Page 189 and 190: Wolfe M. S.1979. Giardiasis. Sympos
Page 191 and 192: APPENDICES APPENDIX 1 Information t
Page 193 and 194: Unayo imvume yokunqaba ukungenela l
Page 195 and 196: Appendix 3 Excystation and culture
Page 197 and 198: Appendix 4 Results of excystation a
Page 199 and 200: Appendix 5 Results of in vitro (aci
Page 201 and 202: Key to Appendix 5 *Replicated inocu
Page 203 and 204: Appendix 7 Preparation of culture m
Page 205 and 206: Appendix 8 List of enzyme systems u
Page 207: Appendix 9 Appendix (9a) Preparatio
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