Next Article in Journal
Phylogenetic Characterization of Marine Benthic Archaea in Organic-Poor Sediments of the Eastern Equatorial Pacific Ocean (ODP Site 1225)
Previous Article in Journal
Coinfection of Chlamydiae and other Bacteria in Reactive Arthritis and Spondyloarthritis: Need for Future Research
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Microorganisms
Volume 4
Issue 3
10.3390/microorganisms4030031
microorganisms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Correia Repeat Enclosed Elements and Non-Coding RNAs in the Neisseria Species

by
Sabrina B. Roberts
1,
Russell Spencer-Smith
1,2,
Mahwish Shah
1,
Jean-Christophe Nebel
3,
Richard T. Cook
1 and
Lori A. S. Snyder
1,*
1
School of Life Sciences, Pharmacy, and Chemistry, Kingston University, Penrhyn Road, Kingston upon Thames, KT1 2EE, UK
2
Department of Pharmacology, University of Illinois at Chicago, Chicago, IL 60612, USA
3
School of Computing and Information Systems, Kingston University, Penrhyn Road, Kingston upon Thames, KT1 2EE, UK
*
Author to whom correspondence should be addressed.
Microorganisms 2016, 4(3), 31; https://doi.org/10.3390/microorganisms4030031
Submission received: 20 July 2016 / Revised: 15 August 2016 / Accepted: 16 August 2016 / Published: 25 August 2016
Browse Figures
Versions Notes

Abstract

:
Neisseria gonorrhoeae is capable of causing gonorrhoea and more complex diseases in the human host. Neisseria meningitidis is a closely related pathogen that shares many of the same genomic features and virulence factors, but causes the life threatening diseases meningococcal meningitis and septicaemia. The importance of non-coding RNAs in gene regulation has become increasingly evident having been demonstrated to be involved in regulons responsible for iron acquisition, antigenic variation, and virulence. Neisseria spp. contain an IS-like element, the Correia Repeat Enclosed Element, which has been predicted to be mobile within the genomes or to have been in the past. This repeat, present in over 100 copies in the genome, has the ability to alter gene expression and regulation in several ways. We reveal here that Correia Repeat Enclosed Elements tend to be near non-coding RNAs in the Neisseria spp., especially N. gonorrhoeae. These results suggest that Correia Repeat Enclosed Elements may have disrupted ancestral regulatory networks not just through their influence on regulatory proteins but also for non-coding RNAs.

Graphical Abstract

1. Introduction

Gonorrhoea poses a global threat that may become virtually untreatable due to antibiotic resistance, including increasing prevalence of azithromycin-resistant isolates [1,2,3,4] resulting in unsuccessful first-line dual treatment with ceftriaxone and azithromycin. Treatment for meningococcal meningitis and septicaemia must be rapid and effective or the infection will be fatal [5,6,7,8]. Concerns over the growing problem of antibiotic resistance in several bacterial species have driven investigations into RNA-based therapeutics to manipulate bacterial gene expression [9,10].
Non-coding RNAs (ncRNAs) can be important regulators of gene expression with roles in both physiology and disease [11,12]. Small ncRNAs have been shown to be involved in regulatory networks and gene expression in the Neisseria spp. [13,14,15,16,17,18,19,20].
Small ncRNA aniS was annotated as a coding sequence (NMB1205 in the meningococcus and NGO0796 in the gonococcus), leading to its inclusion in the design of microarrays that have shown its differential expression [13,21,22,23,24,25,26]. The ncRNA nrrF has been shown to be part of the fur regulon [13,16]. RNA-seq, using next-generation sequencing, has identified several potential ncRNAs due to the depth and specificity of transcript data that can be identified [17,20,27]. As a result, a ncRNA adjacent to pilin gene pilE was identified and shown to be required for pilin antigenic variation [14,19]. Deletion of selected small ncRNAs decreases the virulence of Neisseria meningitidis in the rat model [15]. Eleven of the identified and validated ncRNAs were highly conserved, three were associated with transposable elements, and five were absent from the non-pathogenic Neisseria lactamica. RNA-seq and transposon insertion site sequence mapping identified 253 ncRNAs in Neisseria gonorrhoeae [28]; 59 are intergenic and nine were validated by Northern blotting. Three new ncRNA transcripts were confirmed in the Neisseria gonorrhoeae MS11 strain.
Other non-coding features of the Neisseria spp. genomes are the Correia Repeat Enclosed Elements (CREE) [29]. A N. gonorrhoeae genome contains just over 100 copies [30] of the CREE [30]. N. meningitidis has roughly twice as many CREE within its genome [29,31]. Correia repeats were originally identified as 26 bp sequences often present as inverted repeats [32,33]. CREE are 69–151 bp regions with the Correia inverted repeat and a characteristic core region. These are found most commonly in intergenic regions and are often near virulence, metabolic, and transporter genes [29].
This study investigated whether CREE are located near predicted small ncRNAs in N. gonorrhoeae, N. meningitidis, and N. lactamica. RNA-seq was used to support ncRNA predictions.

2. Materials and Methods

Candidate small ncRNAs were identified using SIPHT [34]. GenBank entries for each of the eight Neisseria spp. investigated here were downloaded on 24 October 2012, accession numbers: N. gonorrhoeae strain NCCP11945 (NC_011035); N. gonorrhoeae strain FA1090 (NC_002946); N. meningitidis strain MC58 (NC_003112); N. meningitidis strain Z2491 (NC_003116); N. meningitidis strain FAM18 (NC_008767); N. meningitidis strain alpha14 (NC_013016); N. meningitidis strain 53442 (NC_010120); N. lactamica strain 020-06 (NC_014752). SIPHT settings used: MaxE 5.00E-3; minimum length 30; maximum length 550; minimum TT confidence 86; and maximum RNAMotif score −6. These are the default settings when a new analysis is launched on the SIPHT web interface (http://newbio.cs.wisc.edu/sRNA/apps/sRNA/submitjob_pegasus_web.php).
The locations of the CREE within N. gonorrhoeae strains FA1090 and NCCP11945 were reported previously [30]. Within N. meningitidis strains MC58, Z2491, FAM18, alpha14, and 053442, and N. lactamica strain 020-06, CREE were identified using the Fuzznuc pattern finder [35] within xBASE [36], as had been done previously for the gonococci [30]. Search terms were based on the previously reported variants of the 26 bp inverted Correia repeat: 5′-tatagtggattaacaaaaaccggtacgg-3′; 5′-tatagtggattaaatttaaaccggtacgg-3′; 5′-tatagtggattaacaaaaatcaggacaa-3′; 5′-tatagtggattaaatttaaatcaggacaa-3′ [30,32,33].
CREE and ncRNA location data was organised in Excel matching CREE with the closest ncRNA for N. gonorrhoeae strain NCCP11945. Statistical analyses used the Kolmogorov-Smirnov test and non-parametric Spearman’s Rho correlation analysis in IBM SPSS Statistics version 21 to assess the distribution of CREE in the genome and between the CREE and ncRNAs.
N. gonorrhoeae strain NCCP11945 was grown on GC agar (Oxoid) at 37°C, 5% CO2 overnight. Growth was immediately removed to RNALater (LifeTechnologies) and RNA extracted using the RNasy kit (Qiagen). RNA quality was determined on the 2100 Bioanalyzer (Agilent) to have a RIN of 9 or above. RNA-seq used the Ion Personal Genome Machine, Ion Total RNA-Seq Kit with ERCC RNA Spike-In Control Mix, Ion Express Template kit, Ion Sequencing kit (Life Technologies), and 1 μg of rRNA-depleted RNA. RNA-seq data (GEO accession numbers GSE58650 and GSE73032) was aligned against the reference genome NCCP11945 using NextGENe v2.3.4.2.

3. Results

Small ncRNAs were predicted using SIPHT [34] for N. gonorrhoeae strains NCCP11945 and FA1090, N. meningitidis strains MC58, Z2491, FAM18, alpha14, and 053442, and N. lactamica strain 020-06 (Table S1 to Table S8). Between 760 and 996 ncRNAs were predicted to be present in these Neisseria spp. genomes (Table 1, Table S1 to Table S8). These results include the known ncRNA nrrF [13,16] (Table S4, Candidate 223–225), the ncRNA adjacent to pilE [14,19] (Table S1, Candidate 468; Table S4, Candidate 182; Table S6, Candidate 880), and aniS [24] (Table S1, Candidate 793; Table S6, Candidate 716;). The aniS sequence is annotated as a putative protein encoding gene in strains FA1090 and MC58 (NGO0796 and NMB1205, respectively). SIPHT uses only intergenic regions for its predictions, therefore the aniS annotation as a CDS excludes it from detection by SIPHT. Annotations as CDSs may account for otherwise conserved ncRNAs being absent from some SIPHT predictions.
CREE locations were previously reported for N. gonorrhoeae strains NCCP11945 and FA1090 [30] (Table 2; Table S9 and Table S10). CREE locations were identified here using the same method for N. meningitidis strains MC58, Z2491, FAM18, alpha14, 53442, and N. lactamica strain 020-05 (Table 2; Table S11 to Table S16). On average, 127 CREE were identified in N. gonorrhoeae and 249 in N. meningitidis. In the single N. lactamica strain 92 were found, similar to previous analyses of non-pathogenic Neisseria spp. [37,38].
The output of SIPHT was combined with the CREE location information for each genome and those within 1000 bp were identified (Table S17 to Table S24). Starting from the distance of 1000 bp, the distances between the CREE and ncRNAs were assessed. This revealed that most of the CREE were within 300 bp of a predicted ncRNA (Table 3). For example, in strain NCCP11945 86 of the 131 CREE are within 300 bp of a predicted ncRNA (66%) (Table 3; Table S17). There are fewer CREE within 300 bp of a predicted ncRNA in the meningococci (average 56%) than in the gonococci (average 71%) and N. lactamica (64%) (Table 3; Table S17 to Table S24).
Many of the CREE overlap the sequences of predicted ncRNAs (Table 3; Table S17 to Table S24). In gonococcal strain NCCP11945, for example, 57% of all of the CREE (75 out of 131) in the genome overlap with predicted ncRNAs (Table 3; Table S17). There are fewer overlaps seen in N. meningitidis and N. lactamica, where on average 37% and 39%, respectively, of all CREE overlap with predicted ncRNAs, compared to a 58% average in N. gonorrhoeae (Table 3).
Using all of the CREE start or end locations for strain NCCP11945 matched to the nearest corresponding ncRNA start or end locations (Table S25), the Kolmogorov- Smirnov test indicated that the CREE locations were not normally distributed (p < 0.001). Using the same test, CREE distribution around the genome was shown to be neither random (Z = 5.292; p < 0.001) nor uniform (Z = 1.557; p = 0.016). Spearman’s Rho correlation demonstrated that CREE locations were very strongly correlated with ncRNA locations (ρ = 1; p < 0.001). The ncRNA locations were all either located within or very close to CREE regions (Figure 1).
Alignment of RNA-seq data against the N. gonorrhoeae strain NCCP11945 genome sequence showed ncRNA transcription (Table S26) at 91 out of 96 locations (95%) where CREE are near to the ncRNAs (Table 3). Read coverage varied: ncRNAs with ≤10 reads were considered low coverage (74 of 91, 81%); >10 to ≤25 were considered medium coverage (3 of 91, 3%); and >25 were considered high coverage (14 of 91, 15%) (Table S26). Genes at high coverage locations included virulence associated genes pilQ, pilin, outer membrane genes, as well as chaperone related genes (Table S27).

4. Discussion

SIPHT predicts between 760 and 996 ncRNAs in the Neisseria spp. genomes investigated present within the 1782 to 2255 intergenic regions (Table 1; Table S1 to Table S8). Amongst these predictions are several previously reported and verified ncRNAs [13,14,16,19,24,25,39], which supports the accuracy of the SIPHT predictions. The predictions reported here include some that span the same region of sequence, where only one is likely to be a ncRNA, and some that may be over-predictions. However, these predictions provide a starting point for investigations into ncRNAs in these species.
Correia Repeat Enclosed Elements are unique to the Neisseria spp. [29,30]. They have been demonstrated to insertionally inactivate genes [31] and to disrupt ancestral regulatory systems through CREE-associated promoters [40]. There are, on average 127 CREE in a N. gonorrhoeae genome, 249 in a N. meningitidis genome, and there are 92 CREE in the N. lactamica strain 050-20 (Table 2; Table S9 to Table S16).
CREE tend to be located within 300 bp of predicted ncRNAs, with many overlapping (Table 3; Table S17 to Table S25). The frequency with which CREE overlap predicted ncRNAs is higher in N. gonorrhoeae (average 58%) than in N. meningitidis (average 37%) and N. lactamica (39%). This is particularly of note because there are only half as many CREE in N. gonorrhoeae, yet those that are present are far more likely to be located close to ncRNAs and to overlap the ncRNA sequences. In N. lactamica, the number of CREE in the genome is closer to that seen in the gonococcus and yet the overlaps between CREE and ncRNAs are on par with N. meningitidis (Table 3). Given the known roles of CREE in gene regulation [40,41,42], it is possible that the presence of CREE and its associated promoters may influence the expression of small ncRNAs through insertional inactivation and/or disruption of ancestral regulatory networks through introduction of CREE-associated promoters.
RNA-seq data supports the SIPHT predictions (Table S26), demonstrating transcription of 95% of the ncRNAs that have adjacent or overlapping CREE in N. gonorrhoeae strain NCCP11945. Those with the highest detected transcription are upstream of virulence determinants (Table S27), further supporting the important role of ncRNAs in these pathogens.

5. Conclusions

In the Neisseria spp., CREE are frequently found near or overlapping ncRNAs in the genome. CREE may influence the expression of ncRNAs through the presence of their promoters and/or insertional activation, similar to the role of CREE in gene regulation. It may be possible to exploit differences between the species with regards to ncRNAs and their interaction with CREE in the design of RNA-based therapies to restrict the meningococcus to the mucosal surface, where it is as harmless as N. lactamica, and to prevent gonococcal antigenic variation, enabling rapid clearance and immunity.

Supplementary Materials

The following are available online at www.mdpi.com/2076-2607/4/3/31/s1, Table S1: SIPHT predicted small non-coding RNAs in Neisseria gonorrhoeae strain NCCP11945, Table S2: SIPHT predicted small non-coding RNAs in Neisseria gonorrhoeae strain FA1090, Table S3: SIPHT predicted small non-coding RNAs in Neisseria meningitidis strain MC58, Table S4: SIPHT predicted small non-coding RNAs in Neisseria meningitidis strain Z2491, Table S5: SIPHT predicted small non-coding RNAs in Neisseria meningitidis strain FAM18, Table S6: SIPHT predicted small non-coding RNAs in Neisseria meningitidis strain alpha14, Table S7: SIPHT predicted small non-coding RNAs in Neisseria meningitidis strain 53442, Table S8: SIPHT predicted small non-coding RNAs in Neisseria lactamica strain 020-06, Table S9: CREE in Neisseria gonorrhoeae strain NCCP11945, Table S10: CREE in Neisseria gonorrhoeae strain FA1090, Table S11: CREE in Neisseria meningitidis strain MC58, Table S12: CREE in Neisseria meningitidis strain Z2491, Table S13: CREE in Neisseria meningitidis strain FAM18, Table S14: CREE in Neisseria meningitidis strain alpha14, Table S15: CREE in Neisseria meningitidis strain 53442, Table S16: CREE in Neisseria lactamica strain 020-06, Table S17: Association of CREE and ncRNAs in Neisseria gonorrhoeae strain NCCP11945, Table S18: Association of CREE and ncRNAs in Neisseria gonorrhoeae strain FA1090, Table S19: Association of CREE and ncRNAs in Neisseria meningitidis strain MC58, Table S20: Association of CREE and ncRNAs in Neisseria meningitidis strain Z2491, Table S21: Association of CREE and ncRNAs in Neisseria meningitidis strain FAM18, Table S22: Association of CREE and ncRNAs in Neisseria meningitidis strain alpha14, Table S23: Association of CREE and ncRNAs in Neisseria meningitidis strain 53442, Table S24: Association of CREE and ncRNAs in Neisseria lactamica strain 020-06, Table S25: Locations of the start or end points of the CREE and the closest predicted ncRNA in Neisseria gonorrhoeae strain NCCP11945, Table S26: RNA-seq data supporting candidacy of ncRNAs with nearby CREE in Neisseria gonorrhoeae strain NCCP11945, Table S27: Genes nearby to CREE that are nearby to ncRNAs in Neisseria gonorrhoeae strain NCCP11945.

Acknowledgments

S.B.R. was the recipient of a Kingston University PhD studentship. R.S.-S. was the recipient of a Kingston University MSc studentship. The authors would like to thank Jonathan Livny of the Broad Institute of MIT and Harvard for his development of SIPHT and Samuel Friedman of the University of Wisconsin-Madison for keeping the system running.

Author Contributions

S.B.R. and L.A.S.S. conceived and designed the experiments; S.B.R. and R.S.-S. performed the experiments; S.B.R., M.S., J.C.N., R.T.C., and L.A.S.S. analyzed the data; R.S.-S. contributed reagents/materials/analysis tools; L.A.S.S. and S.B.R. wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Chisholm, S.A.; Wilson, J.; Alexander, S.; Tripodo, F.; Al-Shahib, A.; Schaefer, U.; Lythgow, K.; Fifer, H. An outbreak of high-level azithromycin resistant Neisseria gonorrhoeae in England. Sex. Transm. Infect. 2016, 92, 365–367. [Google Scholar] [CrossRef] [PubMed]
  2. Tanaka, M.; Furuya, R.; Irie, S.; Kanayama, A.; Kobayashi, I. High prevalence of azithromycin-resistant Neisseria gonorrhoeae isolates with a multidrug resistance phenotype in Fukuoka, Japan. Sex. Transm. Dis. 2015, 42, 337–341. [Google Scholar] [CrossRef] [PubMed]
  3. Demczuk, W.; Martin, I.; Peterson, S.; Bharat, A.; van Domselaar, G.; Graham, M.; Lefebvre, B.; Allen, V.; Hoang, L.; Tyrrell, G.; et al. Genomic epidemiology and molecular resistance mechanisms of azithromycin-resistant Neisseria gonorrhoeae in Canada from 1997 to 2014. J. Clin. Microbiol. 2016, 54, 1304–1313. [Google Scholar] [CrossRef] [PubMed]
  4. Liang, J.Y.; Cao, W.L.; Li, X.D.; Bi, C.; Yang, R.D.; Liang, Y.H.; Li, P.; Ye, X.D.; Chen, X.X.; Zhang, X.B. Azithromycin-resistant Neisseria gonorrhoeae isolates in Guangzhou, China (2009–2013): Coevolution with decreased susceptibilities to ceftriaxone and genetic characteristics. BMC Infect. Dis. 2016, 16, 152. [Google Scholar] [CrossRef] [PubMed]
  5. Hoang, L.M.N.; Thomas, E.; Tyler, S.; Pollard, A.J.; Stephens, G.; Gustafson, L.; McNabb, A.; Pocock, I.; Tsang, R.; Tan, R. Rapid and fatal meningococcal disease due to a strain of Neisseria meningitidis containing the capsule null locus. Clin. Infect. Dis. 2005, 40, e38–e42. [Google Scholar] [CrossRef] [PubMed]
  6. Stephens, D.S.; Greenwood, B.; Brandtzaeg, P. Epidemic meningitis, meningococcaemia, and Neisseria meningitidis. Lancet 2007, 369, 2196–2210. [Google Scholar] [CrossRef]
  7. Caugant, D.A. Genetics and evolution of Neisseria meningitidis: Importance for the epidemiology of meningococcal disease. Infect. Genet. Evol. 2008, 8, 558–565. [Google Scholar] [CrossRef] [PubMed]
  8. Azzari, C.; Nieddu, F.; Moriondo, M.; Indolfi, G.; Canessa, C.; Ricci, S.; Bianchi, L.; Serranti, D.; Poggi, G.M.; Resti, M. Underestimation of Invasive Meningococcal Disease in Italy. Emerg. Infect. Dis. 2016, 22, 469–475. [Google Scholar] [CrossRef] [PubMed]
  9. Dinan, A.M.; Loftus, B.J. Non-translational medicine: Targeting bacterial RNA. Front. Genet. 2013, 4, 230. [Google Scholar] [CrossRef] [PubMed]
  10. Edson, J.A.; Kwon, Y.J. RNAi for silencing drug resistance in microbes toward development of nanoantibiotics. J. Control. Release 2014, 189, 150–157. [Google Scholar] [CrossRef] [PubMed]
  11. Turner, M.; Galloway, A.; Vigorito, E. Noncoding RNA and its associated proteins as regulatory elements of the immune system. Nat. Immunol. 2014, 15, 484–491. [Google Scholar] [CrossRef] [PubMed]
  12. Wagner, E.G.; Romby, P. Small RNAs in bacteria and archaea: Who they are, what they do, and how they do it. Adv. Genet. 2015, 90, 133–208. [Google Scholar] [PubMed]
  13. Mellin, J.R.; Goswami, S.; Grogan, S.; Tjaden, B.; Genco, C.A. A novel fur- and iron-regulated small RNA, NrrF, is required for indirect fur-mediated regulation of the sdhA and sdhC genes in Neisseria meningitidis. J. Bacteriol. 2007, 189, 3686–3694. [Google Scholar] [CrossRef] [PubMed]
  14. Cahoon, L.A.; Seifert, H.S. Transcription of a cis-acting, noncoding, small RNA is required for pilin antigenic variation in Neisseria gonorrhoeae. PLoS Pathog. 2013, 9, e1003074. [Google Scholar] [CrossRef] [PubMed]
  15. Fagnocchi, L.; Bottini, S.; Golfieri, G.; Fantappiè, L.; Ferlicca, F.; Antunes, A.; Guadagnuolo, S.; Del Tordello, E.; Siena, E.; Serruto, D.; et al. Global transcriptome analysis reveals small RNAs affecting Neisseria meningitidis bacteremia. PLoS ONE 2015, 10, e0126325. [Google Scholar] [CrossRef] [PubMed]
  16. Jackson, L.A.; Pan, J.C.; Day, M.W.; Dyer, D.W. Control of RNA stability by NrrF, an iron-regulated small RNA in Neisseria gonorrhoeae. J. Bacteriol. 2013, 195, 5166–5173. [Google Scholar] [CrossRef] [PubMed]
  17. McClure, R.; Balasubramanian, D.; Sun, Y.; Bobrovskyy, M.; Sumby, P.; Genco, C.A.; Vanderpool, C.K.; Tjaden, B. Computational analysis of bacterial RNA-Seq data. Nucleic Acids Res. 2013, 41, e140. [Google Scholar] [CrossRef] [PubMed]
  18. Ramsey, M.E.; Bender, T.; Klimowicz, A.K.; Hackett, K.T.; Yamamoto, A.; Jolicoeur, A.; Callaghan, M.M.; Wassarman, K.M.; van der Does, C.; Dillard, J.P. Targeted mutagenesis of intergenic regions in the Neisseria gonorrhoeae gonococcal genetic island reveals multiple regulatory mechanisms controlling type IV secretion. Mol. Microbiol. 2015, 97, 1168–1185. [Google Scholar] [CrossRef] [PubMed]
  19. Tan, F.Y.; Wörmann, M.E.; Loh, E.; Tang, C.M.; Exley, R.M. Characterization of a novel antisense RNA in the major pilin locus of Neisseria meningitidis influencing antigenic variation. J. Bacteriol. 2015, 197, 1757–1768. [Google Scholar] [CrossRef] [PubMed]
  20. Wachter, J.; Hill, S.A. Small transcriptome analysis indicates that the enzyme RppH influences both the quality and quantity of sRNAs in Neisseria gonorrhoeae. FEMS Microbiol. Lett. 2015, 362, 1–7. [Google Scholar] [CrossRef] [PubMed]
  21. Gunesekere, I.C.; Kahler, C.M.; Ryan, C.S.; Snyder, L.A.; Saunders, N.J.; Rood, J.I.; Davies, J.K. Ecf, an alternative sigma factor from Neisseria gonorrhoeae, controls expression of msrAB, which encodes methionine sulfoxide reductase. J. Bacteriol. 2006, 188, 3463–3469. [Google Scholar] [CrossRef] [PubMed]
  22. Overton, T.W.; Whitehead, R.; Li, Y.; Snyder, L.A.; Saunders, N.J.; Smith, H.; Cole, J.A. Coordinated regulation of the Neisseria gonorrhoeae-truncated denitrification pathway by the nitric oxide-sensitive repressor, NsrR, and nitrite-insensitive NarQ-NarP. J. Biol. Chem. 2006, 281, 33115–33126. [Google Scholar] [CrossRef] [PubMed]
  23. Whitehead, R.N.; Overton, T.W.; Snyder, L.A.; McGowan, S.J.; Smith, H.; Cole, J.A.; Saunders, N.J. The small FNR regulon of Neisseria gonorrhoeae: Comparison with the larger Escherichia coli FNR regulon and interaction with the NarQ-NarP regulon. BMC Genom. 2007, 8, 35. [Google Scholar] [CrossRef] [PubMed]
  24. Fantappiè, L.; Oriente, F.; Muzzi, A.; Serruto, D.; Scarlato, V.; Delany, I. A novel Hfq-dependent sRNA that is under FNR control and is synthesized in oxygen limitation in Neisseria meningitidis. Mol. Microbiol. 2011, 80, 507–523. [Google Scholar] [CrossRef] [PubMed]
  25. Isabella, V.M.; Clark, V.L. Deep sequencing-based analysis of the anaerobic stimulon in Neisseria gonorrhoeae. BMC Genom. 2011, 12, 1–24. [Google Scholar] [CrossRef] [PubMed]
  26. Saunders, N.J.; Davies, J.K. The use of the pan-Neisseria microarray and experimental design for transcriptomics studies of Neisseria. Methods Mol. Biol. 2012, 799, 295–317. [Google Scholar] [PubMed]
  27. Haas, B.J.; Chin, M.; Nusbaum, C.; Birren, B.W.; Livny, J. How deep is deep enough for RNA-Seq profiling of bacterial transcriptomes? BMC Genom. 2012, 13, 734. [Google Scholar] [CrossRef] [PubMed]
  28. Remmele, C.W.; Xian, Y.; Albrecht, M.; Faulstich, M.; Fraunholz, M.; Heinrichs, E.; Dittrich, M.T.; Müller, T.; Reinhardt, R.; Rudel, T. Transcriptional landscape and essential genes of Neisseria gonorrhoeae. Nucleic Acids Res. 2014, 42, 10579–10595. [Google Scholar] [CrossRef] [PubMed]
  29. Snyder, L.A.; Cole, J.A.; Pallen, M.J. Comparative analysis of two Neisseria gonorrhoeae genome sequences reveals evidence of mobilization of Correia Repeat Enclosed Elements and their role in regulation. BMC Genom. 2009, 10, 70. [Google Scholar] [CrossRef] [PubMed]
  30. Liu, S.V.; Saunders, N.J.; Jeffries, A.; Rest, R.F. Genome analysis and strain comparison of correia repeats and correia repeat-enclosed elements in pathogenic Neisseria. J. Bacteriol. 2002, 184, 6163–6173. [Google Scholar] [CrossRef] [PubMed]
  31. Bentley, S.D.; Vernikos, G.S.; Snyder, L.A.; Churcher, C.; Arrowsmith, C.; Chillingworth, T.; Cronin, A.; Davis, P.H.; Holroyd, N.E.; Jagels, K.; et al. Meningococcal genetic variation mechanisms viewed through comparative analysis of serogroup C strain FAM18. PLoS Genet. 2007, 3, e23. [Google Scholar] [CrossRef] [PubMed]
  32. Correia, F.F.; Inouye, S.; Inouye, M. A 26-base-pair repetitive sequence specific for Neisseria gonorrhoeae and Neisseria meningitidis genomic DNA. J. Bacteriol. 1986, 167, 1009–1015. [Google Scholar] [PubMed]
  33. Correia, F.F.; Inouye, S.; Inouye, M. A family of small repeated elements with some transposon-like properties in the genome of Neisseria gonorrhoeae. J. Biol. Chem. 1988, 263, 12194–12198. [Google Scholar] [PubMed]
  34. Livny, J. Bioinformatic discovery of bacterial regulatory RNAs using SIPHT. Methods Mol. Biol. 2012, 905, 3–14. [Google Scholar] [PubMed]
  35. Rice, P.; Longden, L.; Bleasby, A. EMBOSS: The European molecular biology open software suite. Trends Genet. 2000, 16, 276–277. [Google Scholar] [CrossRef]
  36. Chaudhuri, R.R.; Loman, N.J.; Snyder, L.A.S.; Bailey, C.M.; Stekel, D.J.; Pallen, M.J. xBASE2: A comprehensive resource for comparative bacterial genomics. Nucleic Acids Res. 2008, 36, D543–D546. [Google Scholar] [CrossRef] [PubMed]
  37. De Gregorio, E.; Abrescia, C.; Carlomagno, M.S.; di Nocera, P.P. Asymmetrical distribution of Neisseria miniature insertion sequence DNA repeats among pathogenic and nonpathogenic Neisseria strains. Infect. Immun. 2003, 71, 4217–4221. [Google Scholar] [CrossRef] [PubMed]
  38. Marri, P.R.; Paniscus, M.; Weyand, N.J.; Rendón, M.A.; Calton, C.M.; Hernández, D.R.; Higashi, D.L.; Sodergren, E.; Weinstock, G.M.; Rounsley, S.D.; et al. Genome sequencing reveals widespread virulence gene exchange among human Neisseria species. PLoS ONE 2010, 5, e11835. [Google Scholar] [CrossRef] [PubMed]
  39. Huis in ′t Veld, R.A.; Willemsen, A.M.; van Kampen, A.H.; Bradley, E.J.; Baas, F.; Pannekoek, Y.; van der Ende, A. Deep sequencing whole transcriptome exploration of the σE regulon in Neisseria meningitidis. PLoS ONE 2011, 6, e29002. [Google Scholar] [CrossRef] [PubMed]
  40. Rouquette-Loughlin, C.E.; Balthazar, J.T.; Hill, S.A.; Shafer, W.M. Modulation of the mtrCDE-encoded efflux pump gene complex of Neisseria meningitidis due to a Correia element insertion sequence. Mol. Microbiol. 2004, 54, 731–741. [Google Scholar] [CrossRef] [PubMed]
  41. Mazzone, M.; de Gregorio, E.; Lavitola, A.; Pagliarulo, C.; Alifano, P.; di Nocera, P.P. Whole-genome organization and functional properties of miniature DNA insertion sequences conserved in pathogenic Neisseriae. Gene 2001, 278, 211–222. [Google Scholar] [CrossRef]
  42. De Gregorio, E.; Abrescia, C.; Carlomagno, M.S.; di Nocera, P.P. The abundant class of nemis repeats provides RNA substrates for ribonuclease III in Neisseriae. Biochim. Biophys. Acta 2002, 1576, 39–44. [Google Scholar] [CrossRef]
Microorganisms 04 00031 g001 550
Figure 1. Statistical analysis of the associations between CREE and predicted ncRNAs. (a) Using SPSS, CREE locations in N. gonorrhoeae strain NCCP11945 were tested for a normal distribution using the Kolmogorov-Smirnov test. Non-parametric Spearman’s Rho correlation analysis was employed to determine correlation between CREE locations (x-axis) and the SIPHT predicted ncRNA genome sequence locations (y-axis). (b) Statistical analysis of the start/end points of the CREE and the start/end points of the SIPHT predicted ncRNAs shows a close association of these elements in the chromosome. On the x-axis is plotted the distance of the ncRNA to the CREE in basepairs, while on the y-axis are the CREE positions along the N. gonorrhoeae strain NCCP11945 chromosome. This shows that the majority of the CREE are overlapping ncRNAs.
Figure 1. Statistical analysis of the associations between CREE and predicted ncRNAs. (a) Using SPSS, CREE locations in N. gonorrhoeae strain NCCP11945 were tested for a normal distribution using the Kolmogorov-Smirnov test. Non-parametric Spearman’s Rho correlation analysis was employed to determine correlation between CREE locations (x-axis) and the SIPHT predicted ncRNA genome sequence locations (y-axis). (b) Statistical analysis of the start/end points of the CREE and the start/end points of the SIPHT predicted ncRNAs shows a close association of these elements in the chromosome. On the x-axis is plotted the distance of the ncRNA to the CREE in basepairs, while on the y-axis are the CREE positions along the N. gonorrhoeae strain NCCP11945 chromosome. This shows that the majority of the CREE are overlapping ncRNAs.
Microorganisms 04 00031 g001
Table
Table 1. Number of intergenic regions and predicted non-coding RNAs (ncRNAs) in Neisseria spp. genome sequences.
Table 1. Number of intergenic regions and predicted non-coding RNAs (ncRNAs) in Neisseria spp. genome sequences.
StrainIntergenic RegionsSIPHT ncRNAs 1
N. gonorrhoeae strain NCCP119452255760
N. gonorrhoeae strain FA10901806976
N. meningitidis strain MC582015912
N. meningitidis strain Z24911846996
N. meningitidis strain FAM181833959
N. meningitidis strain alpha141782976
N. meningitidis strain 534421881846
N. lactamica strain 020-061873890
1 Number of SIPHT predicted small non-coding RNAs in the genomes (Table S1 to Table S8).
Table
Table 2. Number of Correia Repeat Enclosed Elements in Neisseria spp. genome sequences.
Table 2. Number of Correia Repeat Enclosed Elements in Neisseria spp. genome sequences.
StrainIntergenic RegionsCREE 1
N. gonorrhoeae strain NCCP119452255131
N. gonorrhoeae strain FA10901806123
N. meningitidis strain MC582015248
N. meningitidis strain Z24911846260
N. meningitidis strain FAM181833249
N. meningitidis strain alpha141782255
N. meningitidis strain 534421881234
N. lactamica strain 020-06187392
1 Number of Correia Repeat Enclosed Elements in the genome (Table S9 to Table S16).
Table
Table 3. Correia Repeat Enclosed Elements (CREE) associations with ncRNAs in Neisseria spp. genome sequences.
Table 3. Correia Repeat Enclosed Elements (CREE) associations with ncRNAs in Neisseria spp. genome sequences.
StrainIntergenic RegionsSIPHT ncRNAs 1CREE 2within 1 kb 31 kb % 4within 300 bp 5300 bp % 6Overlap 7Overlap % 8
N. gonorrhoeae strain NCCP1194522557601319673%8666%7557%
N. gonorrhoeae strain FA1090180697612310081%9275%7359%
N. meningitidis strain MC58201591224816466%13153%8735%
N. meningitidis strain Z2491184699626018872%15158%9938%
N. meningitidis strain FAM18183395924918374%14357%9839%
N. meningitidis strain alpha14178297625519175%14758%9537%
N. meningitidis strain 53442188184623415165%12754%8536%
N. lactamica strain 020-061873890927278%5964%3639%
1 Number of SIPHT predicted small non-coding RNAs in the genomes (Tables S1 to S8); 2 Number of Correia Repeat Enclosed Elements in the genome (Table S9 to Table S16); 3 CREE that have one or more SIPHT predicted ncRNAs within 1 kb (Table S17 to Table S24); 4 Percentage of CREE associated with predicted ncRNAs within 1 kb; 5 CREE that have one or more SIPHT predicted ncRNAs within 300 bp (Table S17 to Table S24); 6 Percentage of CREE associated with predicted ncRNA within 300 bp; 7 CREE that overlap one or more SIPHT predicted ncRNAs (Table S17 to Table S24); 8 Percentage of CREE that overlap with predicted ncRNAs.

Share and Cite

MDPI and ACS Style

Roberts, S.B.; Spencer-Smith, R.; Shah, M.; Nebel, J.-C.; Cook, R.T.; Snyder, L.A.S. Correia Repeat Enclosed Elements and Non-Coding RNAs in the Neisseria Species. Microorganisms 2016, 4, 31. https://doi.org/10.3390/microorganisms4030031

AMA Style

Roberts SB, Spencer-Smith R, Shah M, Nebel J-C, Cook RT, Snyder LAS. Correia Repeat Enclosed Elements and Non-Coding RNAs in the Neisseria Species. Microorganisms. 2016; 4(3):31. https://doi.org/10.3390/microorganisms4030031

Chicago/Turabian Style

Roberts, Sabrina B., Russell Spencer-Smith, Mahwish Shah, Jean-Christophe Nebel, Richard T. Cook, and Lori A. S. Snyder. 2016. "Correia Repeat Enclosed Elements and Non-Coding RNAs in the Neisseria Species" Microorganisms 4, no. 3: 31. https://doi.org/10.3390/microorganisms4030031

APA Style

Roberts, S. B., Spencer-Smith, R., Shah, M., Nebel, J.-C., Cook, R. T., & Snyder, L. A. S. (2016). Correia Repeat Enclosed Elements and Non-Coding RNAs in the Neisseria Species. Microorganisms, 4(3), 31. https://doi.org/10.3390/microorganisms4030031

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop