Author(s)
Author(s): Hengxia Fu, Mengmeng Zhang, Jiangnan Qin, Wei Luo, Bin Wang
Download Full PDF
Read Complete Article
DOI: 10.18483/ijSci.1978
~ 29
` 141
a 88-93
Volume 8 - Mar 2019
Abstract
To study the genetic structure of the Stenotrophomonas CRISPR-Cas system using bioinformatics methods. Methods The sequence information of all Stenotrophomonas strains published in the CRISPRdb database was collected, and the CRISPR locus was analyzed using the CRISPRFinder software; All spacers were searched by BLAST platform in the PubMed database to find homologous sequences, and then the relationship between the number of spacer sequences and the number of phages was statistically analyzed. Results According to statistics, 15 confirmed CRISPR structures and 132 questionable CRISPRs were found in 26 strains of Stenotrophomonas, and the repeat sequences of CRISPR structures in different strains were more conservative. Only 1.3% of spacers were homologous with the sequences of known bacteriophages or plasmid in NCBI database. Conclusion The targeted genes of the spacer sequences are mainly from the genome of the bacteria, indicating that the evolution of the Stenotrophomonas CRISPR is related to other bacterial genes. In addition, the negative correlation between the spacer sequence and the number of phages indicates that CRISPR can prevent phage invasion. Analysis of the structure of CRISPR loci in the genome of Stenotrophomonas laid the foundation for further study of drug resistance and genomic stability.
Keywords
Stenotrophomonas, CRISPR-Cas Systems, Repeat Sequence, Spacer Sequence
References
- Alavi, P., Starcher, M.R., Thallinger, G.G. (2014). Stenotrophomonas comparative genomics reveals genes and functions that differentiate beneficial and pathogenic bacteria. BMC Genomics, 15(1): 482-496. doi: 10.1186/1471-2164-15-482.
- Ribitsch, D., Heumann, S., Karl, W. (2012). Extracellular serine proteases from Stenotrophomonas maltophilia: Screening, isolation and heterologous expression in E. coli. J Biotechnol,157(1):140-7. DOI: 10.1016/j.jbiotec.2011.09.025
- Brooke, J.S. (2012). Stenotrophomonas maltophilia: an emerging global opportunistic pathogen. Clin Microbiol Rev,25(1):2-41. doi: 10.1128/CMR.00019-11.
- Karimi, Z., Ahmadi, A., Najafi, A., et al. (2018). Bacterial CRISPR Regions: General Features and their Potential for Epidemiological Molecular Typing Studies. Open. Microbiol. J. 12: 59-70. DOI: 10.2174/1874285801812010059
- Makarova, K.S., Aravind, L., Wolf, Y.I. (2011). Unification of Cas protein families and a simple scenario for the origin and evolution of CRISPR-Cas systems. Biol. Direct. 6:38. DOI: 10.1186/1745-6150-6-38
- Mali, P., Yang, L., Esvelt, K.M., et al. (2013). RNA-guided human genome engineering via Cas9. Science 339: 823-826. DOI: 10.1126/science.1232033
- Wright, A.V., Nuñez, J.K., Doudna, J.A. (2016). Biology and Applications of CRISPR Systems: Harnessing Nature's Toolbox for Genome Engineering. Cell. 164(1-2):29-44. DOI: 10.1016/j.cell.2015.12.035.
- Rahmatabadi, S.S., Nezafat, N., Negahdaripour, M., et al. (2016). Studying the features of 57 confirmed CRISPR loci in 29 strains of Escherichia coli, J. Basic. Microbiol. 56: 645-653. DOI: 10.1002/jobm.201500707.
- Zhao, X., Yu, Z., Xu, Z. (2018). Study the Features of 57 Confirmed CRISPR Loci in 38 Strains of Staphylococcus aureus. Front Microbiol. 9:1591. DOI: 10.3389/fmicb.2018.01591.
- Shariat, N., Timme, R.E., Pettengill, J.B. (2015). Characterization and evolution of Salmonella CRISPR-Cas systems. Microbiology. 161(2):374-386. doi: 10.1099/mic.0.000005.
- Grissa, I., Vergnaud, G., Pourcel, C. (2007). The CRISPRdb database and tools to display CRISPRs and to generate dictionaries of spacers and repeats. BMC. Bioinformatics. 8 :172. DOI: 10.1186/1471-2105-8-172
- Redman, M., King, A., Watson, C. (2016). What is CRISPR/Cas9? Arch Dis Child Educ Pract Ed. 101(4):213-5. Redman, M., King, A., Watson, C. (2016). What is CRISPR/Cas9? Arch Dis Child Educ Pract Ed. 101(4):213-5.
- Barrangou, R., Fremaux, C., Deveau, H. (2007). CRISPR provides acquired resistance against viruses in prokaryotes. Science. 315(5819):1709-12. DOI: 10.1126/science.1138140
- Marraffini, L.A., Sontheimer, E.J. (2008). CRISPR interference limits horizontal gene transfer in staphylococci by targeting DNA. Science. 322 (5909): 1843-5. DOI: 10.1126/science.1165771
- Jiang, W., Maniv, I., Arain, F. (2013). Dealing with the evolutionary downside of CRISPR immunity: bacteria and beneficial plasmids. PLoS Genet. 9(9): e1003844. DOI: 10.1371/journal.pgen.1003844
- Reed, F.A. (2017). CRISPR/Cas9 Gene Drive: Growing Pains for a New Technology. Genetics. 205(3):1037-1039. doi: 10.1534/genetics.116.198887.
- Hille, F., Richter, H., Wong, SP., Bratovič, M., Ressel, S., Charpentier, E. (2018). The Biology of CRISPR-Cas: Backward and Forward. Cell. 172 (6): 1239-1259. doi: 10.1016/j.cell.2017.11.032.
- Hauben, L., Vauterin, L., Moore, E., Hoste, B., Swings, J. (1999). Genomic diversity of the genus Stenotrophomonas. Int J Syst Bacteriol. 49 (4): 1749-60. DOI: 10.1099/00207713-49-4-1749
- van, Belkum, A., Soriaga, L.B., LaFave, M.C. (2015). Phylogenetic Distribution of CRISPR-Cas Systems in Antibiotic-Resistant Pseudomonas aeruginosa. MBio. 6: e01796-1815. DOI: 10.1128/mBio.01796-15
- Kunin, V., Sorek, R., Hugenholtz, P. (2007). Evolutionary conservation of Sequence and secondary structures in CRISPR repeats, Genome. Biol. 8: R61. DOI: 10.1186/gb-2007-8-4-r61
- Yang, S., Liu, J., Shao, F. (2015). Analysis of the features of 45 identified CRISPR loci in 32 Staphylococcus aureus. Biochem. Biophys. Res. Commun. 464 :894-900. doi: 10.1016/j.bbrc.2015.07.062.
- Barrangou, R., Marraffini, L.A. (2014). CRISPR-Cas systems: Prokaryotes upgrade to adaptive immunity. Molecular Cell. 54 (2): 234–44. doi: 10.1016/j.molcel.2014.03.011.
- Nozawa, T., Furukawa, N., Aikawa, C. (2011). CRISPR inhibition of prophage acquisition in Streptococcus pyogenes. PLoS One. 6(5): e19543. doi: 10.1371/journal.pone.0019543.
Cite this Article:
International Journal of Sciences is Open Access Journal.
This article is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) License.
Author(s) retain the copyrights of this article, though, publication rights are with Alkhaer Publications.