CC BY-NC-ND 4.0 · J Lab Physicians 2009; 1(01): 002-006
DOI: 10.4103/0974-2727.54800
Review Article

Progress of Science from Microscopy to Microarrays (Part 1): Diagnosis of Parasitic Diseases

Ayan Dey
Division of Clinical Microbiology, Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi-110 029, India
,
Sarman Singh
Division of Clinical Microbiology, Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi-110 029, India
› Author Affiliations
Source of Support: Nil

ABSTRACT

Even though description of the magnifying glass goes back to 1021 by an Arabic physicist in his book, Antony van Leeuwenhoek was the first man to improve the then simple microscope for viewing biological specimens in 1674. This suggests that every discovery has scope for improvement, be it physics or be it biology. In the field of biology, scientists have long studied gene expression as a hallmark of gene activities reflecting the current cell conditions and response to host immune defense systems. These studies have been cumbersome, technically demanding and time-consuming. Application of microarrays has revolutionized this field and help understand the simultaneous expression of thousands of genes in a single sample put onto a single solid support. It is also now possible to compare gene expression in two different cell types, different stages of life cycle or two tissue samples, such as in healthy and diseased ones. Thus microarrays are beginning to dominate other conventional and molecular diagnostic technologies. The microarrays consist of solid supports onto which the nucleic acid sequences from thousands of different genes are immobilized, or attached at fixed locations. These solid supports themselves are usually glass slides, silicon chips or nylon membranes. The nucleic acids are spotted or synthesized directly onto the support. Application of microarrays is new for parasites. Most of these applications are done for monitoring parasite gene expression, to predict the functions of uncharacterized genes, probe the physiologic adaptations made under various environmental conditions, identify virulence-associated genes and test the effects of drug targets. The best examples are vector-borne parasites, such as Plasmodium, Trypanosoma and Leishmania, in which genes expressed, during mammalian and insect host stages, have been elucidated. Microarrays have also been successfully applied to understand the factors responsible to induce transformation from tachyzoite-to-bradyzoite and vice versa in Toxoplasma gondii. Thus microarrays provide a novel tool for diagnosis, prognosis and clinical management of infectious disease.



Publication History

Article published online:
29 January 2020

© 2009.

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  • REFERENCES

  • 1 Slonim DK. From patterns to pathways: gene expression data analysis comes of age. Nat Genet 2002;32:502-8.
  • 2 Chizhikov V, Rasooly A, Chumakov K, Levy DD. Microarray analysis of microbial virulence factors. Appl Environ Microbiol 2001;67:3258-63.
  • 3 Ben Mamoun C, Gluzman IY, Hott C, MacMillan SK, Amarakone AS, Anderson DL, et al. Co-ordinated programme of gene expression during asexual intraerythrocytic development of the human malaria parasite Plasmodium falciparum revealed by microarray analysis. Mol Microbiol 2001;39:26-36.
  • 4 Beverley SM, Akopyants NS, Goyard S, Matlib RS, Gordon JL, Brownstein BH, et al. Putting the Leishmania genome to work: functional genomics by transposon trapping and expression profiling. Philos Trans R Soc Lond B Biol Sci 2002;357:47-53.
  • 5 Bozdech Z, Zhu J, Joachimiak MP, Cohen FE, Pulliam B, DeRisi JL . Expression profiling of the schizont and trophozoite stages of Plasmodium falciparum with a long-oligonucleotide microarray. Genome Biol 2003;4:R9.
  • 6 Cleary MD, Singh U, Blader IJ, Brewer JL, Boothroyd JC. Toxoplasma gondii asexual development: identification of developmentally regulated genes and distinct patterns of gene expression. Eukaryot Cell 2002;1:329-40.
  • 7 Diehl S, Diehl F, El-Sayed NM, Clayton C, Hoheisel JD. Analysis of stage-specific gene expression in the bloodstream and the procyclic form of Trypanosoma brucei using a genomic DNA-microarray. Mol Biochem Parasitol 2002;123:115-23.
  • 8 Hayward RE, DeRisi JL, Alfadhli S, Kaslow DC, Brown PO, Rathod PK. Shotgun DNA microarrays and stage-specific gene expression in Plasmodium falciparum malaria. Mole Microbiol 2000;35:6-14.
  • 9 Singh U, Brewer JL, Boothroyd JC . Genetic analysis of tachyzoite to bradyzoite differentiation mutants in Toxoplasma gondii reveals a hierarchy of gene induction. Mol Microbiol 2002;44:721-33.
  • 10 Minning TA, Bua J, Garcia GA, McGraw RA, Tarleton RL. Microarray profiling of gene expression during trypomastigote to amastigote transition in Trypanosoma cruzi. Mol Biochem Parasitol 2003;131:55-64.
  • 11 Saxena A, Worthey EA, Yan S, Leland A, Stuart KD, Myler PJ. Evaluation of differential gene expression in Leishmania major Friedlin procyclics and metacyclics using DNA microarray analysis. Mol Biochem Parasitol 2003;129:103-14.
  • 12 Singh S., Dey A, Sivakumar R. Applications of Molecular Methods for Leishmania control. Expert Rev Mol Diagn 2005;5:251-65.
  • 13 Wang Z, Vora GJ, Stenger DA. Detection and Genotyping of Entamoeba histolytica, Entamoeba dispar, Giardia lamblia, and Cryptosporidium parvum by Oligonucleotide Microarray. J Clin Mirobiol 2004;42:3262-71.
  • 14 Wang Z, Orlandi PA, Stenger DA. Simultaneous detection of four human pathogenic Microsporidian Species from clinical samples by oligonucleotide microarray. J Clin Microbiol 2005;43:4121-8.
  • 15 Franzen C, Muller A. Molecular techniques for detection, species differentiation, and phylogenetic analysis of microsporidia. Clin Microbiol Rev 1999;12:243-85.
  • 16 Garcia LS. Laboratory identification of the microsporidia. J Clin Microbiol 2002;40:1892-901.
  • 17 Orlandi PA, Lampel KA. Extraction-free, filter-based template preparation for rapid and sensitive PCR detection of pathogenic parasitic protozoa. J Clin Microbiol 2000;38:2271-7.
  • 18 Subrungruang I, Mungthin M, Chavalitshewinkoon-Petmitr P, Rangsin R, Naaglor T, Leelayoova S. Evaluation of DNA extraction and PCR methods for detection of Enterocytozoon bienuesi in stool specimens. J Clin Microbiol 2004;42:3490-4.
  • 19 Duncan R. DNA microarray analysis of protozoan parasite gene expression: outcomes correlate with mechanisms of regulation. Trends Parasitol 2004;20:211-6.