Volume 12, Number 3—March 2006
Research
Identifying and Quantifying Genotypes in Polyclonal Infections due to Single Species
Table 4
Pathogen | Genomic site of variation | Observed size variations | Reference |
---|---|---|---|
Plasmodium falciparum | Block 2 variable region of merozoite surface protein 1 (msp1), PCR | 150–200 bp with multiple 9-bp insertions and deletions based on number of tripeptide repeats | (14) |
Dengue | 3´ NCR after the NS5 stop codon | 2–14 and 75-nt deletions, 4 copies of 8-nt imperfect repeat | (16) |
Yellow fever virus | 3´ NCR | 216-nt duplication, 40-nt deletion (repeat hairpin motif) | (17) |
HIV | env gene | 35- and 48-nt insertions, 21- and 36-nt deletions | (18) |
gp120 V3 and V4 loops | 9- and 12-nt deletions | (19) | |
Mycobacterium tuberculosis | Novel IS6110 insertions† | 36-bp DRs interspersed with variable spacers for DVRs | (20) |
VNTRs | Repeating units of 53–79 bp with 16–17 copies | (21) | |
Genomic deletions | Based on genomic microarrays | (21) | |
Bacillus anthracis | MLVA† | Variations of 12, 9, 18, 72, and 5 bp for MLVA markers vrrA, vrrB1, vrrB2, vrrC2, and CG3 | (23) |
Subtyping of 2001 bioterrorism organism | All isolates were genotype 62 | (24) | |
Yersinia pestis | MLVA† with 25 markers for tandem repeat loci with 9–60 bp repeats of 3–36 units | Amplicon sizes for complete alleles ranging from 119 to 786 bp | (25) |
Smallpox virus | Coding regions of the viral genome | Variable numbers of 9- and 21-bp repeats (n = 5–31 and 15–38, respectively), insertions of 32 and 464 bp and a 251-bp deletion | (26) |
Inverted terminal repeats between nonrepetitive elements 1 and 2 (NR1, NR2) | 0–4 copies of a 69-bp sequence | ||
Potential virulence proteins | Smallpox inhibitor of complement enzymes, chemokine-binding protein II, and Z-DNA binding protein | (27) |
*PCR, polymerase chain reaction; NCR, noncoding region; DRs, direct repeats; DVRs, direct variant repeats; VNTRs, variable numbers tandem repeats; MLVA, multiple locus VNTR analysis; msp1, merozoite surface protein 1.
†Exists at multiple sites within the pathogen genome.
References
- Janini LM, Tanuri A, Schechter M, Pweralta JM, Vicente AC, Dela Torre N, Horizontal and vertical transmission of human immunodeficiency virus type 1 dual infections caused by viruses of subtypes B and C. J Infect Dis. 1998;177:227–31. DOIPubMedGoogle Scholar
- Rayfield MA, Downing RG, Baggs J, Hu DJ, Pieniazek D, Luo C-C, A molecular epidemiologic survey of HIV in Uganda. AIDS. 1998;12:521–7. DOIPubMedGoogle Scholar
- Tuveri R, Rothschild C, Pol S, Reijasse D, Persico T, Gazengel C, Hepatitis C virus genotypes in French hemophiliacs: kinetics and reappraisal. J Med Virol. 1997;51:36–41. DOIPubMedGoogle Scholar
- Walling DW, Shebib N, Weaver SC, Nichols CM, Flaitz CM, Webster-Cyriaque J. The molecular epidemiology and evolution of Epstein-Barr virus: sequence variation and genetic recombination in the latent membrane protein-1 gene. J Infect Dis. 1999;179:763–74. DOIPubMedGoogle Scholar
- Loroño-Pino MA, Cropp CB, Farfán JA, Vorndam AV, Rodríguez-Angulo EM, Rosado-Paredes EP, Common occurrence of concurrent infections by multiple dengue virus serotypes. Am J Trop Med Hyg. 1999;61:725–30.PubMedGoogle Scholar
- Warren RM, Victor TC, Streicher EM, Richardson M, Beyers N, Gey van Pittius N, Patients with active tuberculosis often have different strains in the same sputum specimen. Am J Respir Crit Care Med. 2004;169:610–4. DOIPubMedGoogle Scholar
- Pavlic M, Allerberger F, Dierich MP, Prodinger WM. Simultaneous infection with two drug-susceptible Mycobacterium tuberculosis strains in an immunocompetent host. J Clin Microbiol. 1999;37:4156–7.PubMedGoogle Scholar
- Wittwer CT, Herrmann MG, Moss AA, Rasmussen RP. Continuous fluorescence monitoring of rapid cycle DNA amplification. Biotechniques. 1997;22:134–8.PubMedGoogle Scholar
- Halford WP, Falco VC, Gebhardt BM, Carr DJ. The inherent quantitative capacity of the reverse transcription-polymerase chain reaction. Anal Biochem. 1999;266:181–91. DOIPubMedGoogle Scholar
- Trager W, Jensen JB. Human malaria parasites in continuous culture. Science. 1976;193:673–5. DOIPubMedGoogle Scholar
- Campbell CC, Collins WE, Milhous WK, Roberts JM, Armstead A. Adaptation of the Indochina I/CDC strain of Plasmodium falciparum to the squirrel monkey (Saimiri sciureus). Am J Trop Med Hyg. 1986;35:472–5.PubMedGoogle Scholar
- Teklehaimanot A, Nguyen-Dinh P, Collins WE, Barber AM, Campbell CC. Evaluation of sporontocidal compounds using gametocytes produced in vitro. Am J Trop Med Hyg. 1985;34:429–4.PubMedGoogle Scholar
- del Portillo HA, Nussenzweig RS, Enea V. Circumsporozoite gene of Plasmodium falciparum strain from Thailand. Mol Biochem Parasitol. 1987;24:289–4. DOIPubMedGoogle Scholar
- Miller LH, Roberts T, Shahabuddin M, McCutchan TF. Analysis of sequence diversity in the P. falciparum merozoite surface protein-1 (MSP-1). Mol Biochem Parasitol. 1993;59:1–14. DOIPubMedGoogle Scholar
- Davis CL, Field D, Metzgar D, Saiz R, Morin PA, Smith IL, Numerous length polymorphisms at short tandem repeats in human cytomegalovirus. J Virol. 1999;73:6265–70.PubMedGoogle Scholar
- Shurtleff AC, Beasley DWC, Chen JJY, Ni H, Suderman MT, Wang H, Genetic variation in the 3´ non-coding region of dengue viruses. Virology. 2001;187:75–87. DOIPubMedGoogle Scholar
- Bryant JE, Vasconcelos PFC, Rijnbrand RCA, Mutebi JP, Higgs S, Barrett ADT. Size heterogeneity in the 3´ noncoding region of South American isolates of yellow fever virus. J Virol. 2005;79:3807–21. DOIPubMedGoogle Scholar
- Starcich BR, Hahn BH, Shaw G, McNeely PD, Medrow S, Wolf H, Identification and characterization of conserved and variable regions in the envelope gene of HTLV-III/LAV, the retrovirus of AIDS. Cell. 1986;45:637–48. DOIPubMedGoogle Scholar
- Delwart E, Magierowska M, Royz M, Foley B, Peddada L, Smith R, Homogeneous quasispecies in 16 out of 17 individuals during very early HIV-1 primary infection. AIDS. 2002;16:189–95. DOIPubMedGoogle Scholar
- Mokrousov I, Narvaskaya O, Limeschenko E, Otten T, Vyshnevskiy B. Novel IS6110 insertion sites in the direct repeat locus of Mycobacterium tuberculosis clinical strains from the St. Petersburg area of Russia and evolutionary and epidemiological considerations. J Clin Microbiol. 2002;40:1504–7. DOIPubMedGoogle Scholar
- Frothingham R, Meeker-O'Connell WA. Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats. Microbiology. 1998;144:1189–96. DOIPubMedGoogle Scholar
- de la Salmonière Y-OLG, Kim CC, Tsolaki AG, Pym AS, Siegrist MS, Small PM. High-throughput method for detecting genomic deletion polymorphisms. J Clin Microbiol. 2004;42:2913–8. DOIPubMedGoogle Scholar
- Gierczynski R, Kaluzewski S, Rakin A, Jagielski M, Zasada A, Jakubczak A, Intriguing diversity of Bacillus anthracis in eastern Poland—the molecular echoes of the past outbreaks. FEMS Microbiol Lett. 2004;239:235–40. DOIPubMedGoogle Scholar
- Hoffmaster AR, Fitzgerald CC, Ribot E, Mayer LW, Popovic T. Molecular subtyping of Bacillus anthracis and the 2001 bioterrorism-associated anthrax outbreak, United States. Emerg Infect Dis. 2002;8:1111–6.PubMedGoogle Scholar
- Pourcel C, Andrè-Mazeaud F, Neubauer H, Ramisse F, Vergnaud G. Tandem repeats analysis for the high resolution phylogenetic analysis of Yersinia pestis. BMC Microbiol. 2004;4:22. DOIPubMedGoogle Scholar
- Massung RF, Loparev VN, Knight JC, Totmenin AV, Chizhikov VE, Parsons JM, Terminal region sequence variations in variola virus DNA. Virology. 1996;221:291–300. DOIPubMedGoogle Scholar
- Massung RF, Esposito JJ, Liu L-I, Qi J, Utterback TR, Knight JC, Potential virulence determinants in terminal regions of variola smallpox virus genome. Nature. 1993;366:748–51. DOIPubMedGoogle Scholar
- de la Puente-Redondo VA, del Blanco NG, Gutiérrez-Martín CB, García-Peña FJ, Rodriguez Ferri EF. Comparison of different PCR approaches for typing of Franciscella tularensis strains. J Clin Microbiol. 2000;38:1016–22.PubMedGoogle Scholar
- Farlow J, Smith KL, Wong J, Abrams M, Lytle M, Keim P. Francisella tularensis strain typing using multiple-locus variable-number tandem repeat analysis. J Clin Microbiol. 2001;39:3186–92. DOIPubMedGoogle Scholar
- Nachamkin I, Panaro NJ, Li M, Ung H, Yuen PK, Kricka LJ, Agilent 2100 bioanalyzer for restriction fragment length polymorphism analysis of the Campylobacter jejuni flagellin gene. J Clin Microbiol. 2001;39:754–7. DOIPubMedGoogle Scholar
- Snounou G, Farnert A. Genotyping of Plasmodium falciparum parasites by PCR: msp1, msp2 and glurp. In: Ljungström I, Perlmann H, Schlichtherle M, Scherf A, Washlgren M, editors. Methods in malaria research. 4th ed. Manassas (VA): Malaria Research and Reference Resource Center and American Type Culture; 2004. p. 221–5. Available from http://www.malaria.mr4.org/Protocol_Book/Methods_In_Malaria_Research.pdf
- Willmore C, Holden JA, Zhou L, Tripp S, Witwer CT, Layfield LJ. Detection of c-kit activating mutations in gastrointestinal stromal tumors by high-resolution amplicons melting analysis. Am J Clin Pathol. 2004;122:206–16. DOIPubMedGoogle Scholar
- Ye P, Parra EJ, Sosnoski DM, Hiester K, Underhill PA, Shriver MD. Melting curve SNP (McSNP) genotyping: a useful approach for diallelic genotyping in forensic science. J Forensic Sci. 2002;47:593–600.PubMedGoogle Scholar
- Witt H, Landt O. Rapid detection of the Wilson's disease H1069Q mutation by melting curve analysis with the LightCycler. Clin Chem Lab Med. 2001;39:953–5. DOIPubMedGoogle Scholar
- Pals G, Young C, Mao HS, Worsham MJ. Detection of a single base substitution in a single cell using the LightCycler. J Biochem Biophys Methods. 2001;47:121–9. DOIPubMedGoogle Scholar
- Hill MD, Lorenzo E, Kumar A. Changes in the human immunodeficiency virus V3 region that correspond with disease progression: a meta-analysis. Virus Res. 2004;106:27–33. DOIPubMedGoogle Scholar
- Daniels RS, Wilson P, Patel D, Longhurst H, Patterson S, Analysis of full-length HIV type 1 env genes indicates differences between the virus infecting T cells and dendritic cells in peripheral blood of infected patients. AIDS Res Hum Retroviruses. 2004;20:409–13. DOIPubMedGoogle Scholar
- Jensen MA, van't Wout AB. Predicting HIV-1 coreceptor usage with sequence analysis. AIDS Rev. 2003;5:104–12.PubMedGoogle Scholar
- Zeuzem S. Hepatitis C virus: kinetics and quasispecies evolution during anti-viral therapy. Forum. 2000;10:32–42.PubMedGoogle Scholar
- Iwasa Y, Michor F, Nowak MA. Virus evolution within patients increases pathogenicity. J Theor Biol. 2005;232:17–26. DOIPubMedGoogle Scholar
Page created: January 27, 2012
Page updated: January 27, 2012
Page reviewed: January 27, 2012
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.