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Meng, X.;  He, M.;  Xia, P.;  Wang, J.;  Wang, H.;  Zhu, G. Small Non-Coding RNAs in Salmonella–Host Interactions. Encyclopedia. Available online: https://encyclopedia.pub/entry/27236 (accessed on 26 December 2024).
Meng X,  He M,  Xia P,  Wang J,  Wang H,  Zhu G. Small Non-Coding RNAs in Salmonella–Host Interactions. Encyclopedia. Available at: https://encyclopedia.pub/entry/27236. Accessed December 26, 2024.
Meng, Xia, Mengping He, Pengpeng Xia, Jinqiu Wang, Heng Wang, Guoqiang Zhu. "Small Non-Coding RNAs in Salmonella–Host Interactions" Encyclopedia, https://encyclopedia.pub/entry/27236 (accessed December 26, 2024).
Meng, X.,  He, M.,  Xia, P.,  Wang, J.,  Wang, H., & Zhu, G. (2022, September 16). Small Non-Coding RNAs in Salmonella–Host Interactions. In Encyclopedia. https://encyclopedia.pub/entry/27236
Meng, Xia, et al. "Small Non-Coding RNAs in Salmonella–Host Interactions." Encyclopedia. Web. 16 September, 2022.
Small Non-Coding RNAs in Salmonella–Host Interactions
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This entry is adapted from the peer-reviewed paper 10.3390/biology11091283

Salmonella species infect hosts by entering phagocytic and non-phagocytic cells, causing diverse disease symptoms, such as fever, gastroenteritis, and even death. Therefore, Salmonella has attracted much attention. Many factors are involved in pathogenesis, for example, the capsule, enterotoxins, Salmonella pathogenicity islands (SPIs), and corresponding regulators. These factors are all traditional proteins associated with virulence and regulation. Small non-coding RNAs (sRNAs) have also been reported to function as critical regulators. Salmonella has become a model organism for studying sRNAs. sRNAs regulate gene expression by imperfect base-pairing with targets at the post-transcriptional level. sRNAs are involved in diverse biological processes, such as virulence, substance metabolism, and adaptation to stress environments. 

sRNAs Salmonella host interactions

1. Introduction

Salmonella enterica is one of the leading causes of foodborne gastroenteritis worldwide. The two most important serovars of Salmonella are Salmonella enterica serovar Typhimurium (S. Typhimurium) and Salmonella enterica serovar Enteritidis (S. Enteritidis), which cause non-typhoid salmonellosis infections [1]. As an intracellular zoonotic pathogen, Salmonella regularly infects hosts. It enters the stomach and intestinal lumen of the host after ingestion of contaminated food, causing gastroenteritis in both humans and animals as well as typhoid fever in mice. Salmonella must survive within the acidic environment of the stomach and penetrates the gut barrier via M cells in Peyer’s patches of the intestine [2]. Salmonella invades the cell membrane and forms Salmonella-containing vacuoles (SCVs) with the help of a Type III secretion system (T3SS) encoded by Salmonella pathogenicity islands (SPIs) [3]. After that, macrophages engulf the bacteria and kill them to resist infection by producing reactive nitrogen species (RNS) and reactive oxygen species (ROS) [4]. Interestingly, Salmonella employs sophisticated strategies to survive and replicate inside phagocytic and non-phagocytic cells, causing serious diseases in humans and animals.
The small non-coding RNAs (sRNAs), which are known to be involved in the regulation of gene expression, have a length of 50–500 nucleotides and have been found in various bacteria, for example, Escherichia coli, Listeria monocytogenes, and S. Typhimurium [5][6]. Based on their mode of base-pairing, they are classified into cis- and trans-encoded sRNAs. Cis-encoded sRNAs are transcribed from the same loci as the mRNAs on the opposite strand of DNA and bind to their cognate mRNA targets with perfect complementarity, resulting in either transcriptional termination or translational initiation. Trans-encoded sRNAs interact with multiple mRNA targets through imperfect complementation [6][7]. Gene expression is usually regulated by trans-acting sRNAs at the post-transcriptional level [8]. The functions of more than half of the trans-acting sRNAs require the chaperone protein Hfq, which plays an important role in regulation by stabilizing sRNAs and mediates their interaction with the trans-encoded target mRNAs of host cells, leading to repression of translation or acceleration of mRNA decay [9]. S. Typhimurium expresses hundreds of sRNAs, many of which are activated under special stress and virulence conditions, suggesting that sRNAs are an important component of regulatory networks controlling gene expression in bacteria during host infection [10].
sRNAs regulate many physiological processes in bacteria, including metabolism, iron homeostasis, quorum sensing, outer membrane protein biosynthesis, and the regulation of virulence genes [11][12]. In recent years, attention has been focused on the functions of sRNAs in bacteria–host interactions. To establish a successful infection, Salmonella must first resist the acidic environment and oxidative stress, adhere to and invade non-phagocytic cells, and finally evade host immunity to survive inside macrophages [13]. sRNAs play integral roles in bacterial stress responses, promote intracellular survival, and modulate host immune responses [9][14]. In this entry, researchers summarize the roles of sRNAs in the interaction between Salmonella and host cells (see Table 1 for a summary of sRNAs), aiming to understand the roles of sRNAs upon host cell infection, provide an overview of the functional mechanisms of sRNAs, and provide ideas to improve host resistance to Salmonella infection.
Table 1. Summarized characteristics of sRNAs during Salmonella–host interactions.
Function in Infection Serotype sRNA Description Target Gene/Protein Reference
Resisting AcidEnvironment S. Typhimurium SB300 DsrA Trans-coded rpoS [15]
S. Typhimurium RyeC Trans-coded ptsi [16]
S. Typhimurium 6S RNA Trans-coded citGXFED, nuo operon [17]
Adhering and Invading to Non-Phagocytic Cells S. Enteritidis 50336 STnc640 Trans-coded fimA [18][19]
S. Typhimurium MicC Trans-coded OmpD [20][21]
S. Enteritidis InvR Trans-coded OmpD [22]
S. Typhimurium IsrJ Trans-coded SptP [23]
Salmonella IsrM Trans-coded HilE [24]
S. Enteritidis 50336 RyhB-1, RyhB-2 Trans-coded sipA, sopE [25]
S. Typhimurium InvS Trans-coded PrgH, FimZ [26]
  Salmonella PinT Trans-coded hilA, rtsA [27]
Resisting Oxidative Stress S. Enteritidis 2472 Sal-1 Trans-coded iNOS [28]
S. Typhimurium OxyS cis-coded ompX [29]
S. Typhimurium CyaR Trans-coded ompX [29]
S. Typhimurium MicA Trans-coded ompX [29]
S. Typhimurium YK5104 RaoN Trans-coded ldhA [29]
S. Typhimurium RyhB-1, RyhB-2 Trans-coded - [23][30]
Survivalin Macrophages S. Typhimurium IsrC cis-coded msgA [23]
S. Typhimurium IsrN cis-coded STM2765 [23]
S. Typhimurium OxyS cis-coded - [23]
S. Typhi RfrA, RfrB Trans-coded - [31]
S. Typhimurium RyhB-1, RyhB-2 Trans-coded fumA, sdhD [32]
S. Typhimurium IsrM Trans-coded SopA [24]
  S. Typhimurium YK5104 RaoN Trans-coded - [30][33]
Regulating Inflammatory Cytokines of Hosts S. Typhimurium PinT Trans-coded IL-8, SOCS3 [34][35]

2. sRNAs’ Functions in Salmonella–Host Interactions

2.1. sRNAs Regulate Resistance to the Acidic Environment

Acid stress is one of the most important stresses that Salmonella must overcome to colonize the host. Salmonella may encounter acidic environments such as the stomach, and acid exposure also occurs after invading the intestinal mucosa [13][36]. Interestingly, Salmonella has evolved a precise response known as the acid tolerance response (ATR), which promotes the survival of acid-adapted cells at low pH levels [36]. The alternative sigma factor RpoS, which is a global regulator of gene expression when bacteria suffer from starvation or other stress conditions, is required for Salmonella resistance to acid stress [37]. Recently, sRNAs have been identified as major regulators of acid stress response networks. The 87-nucleotide sRNA DsrA, which is present in both Salmonella and E. coli, is a regulator of acid resistance. DsrA expression can be induced in S. Typhimurium in a minimum essential medium, with maximum induction at pH 3.1. Deletion of dsrA reduced the effectiveness of the ATR, resulting in a lower survival rate in acidic environments [38]. Although how DsrA modulates the acid stress response is still unclear, some evidence has proven that DsrA could regulate the translation of RpoS and the expression of some acid resistance genes [15][39][40]. DsrA activates the translation of RpoS by base-pairing with the upstream leader portion of rpoS mRNA in S. Typhimurium [15]. Mutations in dsrA decreased the expression of RpoS in exponential and stationary phases of E. coli [39]. The mRNA levels of multiple acid resistance genes in the hdeAB, gadAX, and gadBC operons were increased with DsrA overproduction in E. coli [40]. The above reports are useful for further study of the mechanism of acid resistance regulation through DsrA. Besides the acid stress response, DsrA enhances the invasive phenotype of S. Typhimurium by repressing the translation of the histone-like nucleoid protein (H-NS) [15][38]. Moreover, deletion of dsrA reduced the motility, adhesion, and invasion efficacy of S. Typhimurium [38]. Another example is the sRNA RyeC, which is the antitoxin component of a type I toxin–antitoxin (TA) system that is encoded by a small ORF and is associated with extremely high toxicity [41]. Overexpression of the trans-encoded RyeC in S. Typhimurium during the ATR inhibits the expression of the target PtsI, which is a subunit of a major carbohydrate transporter, through direct interaction at the post-transcriptional level, resulting in a reduced ATR in Salmonella [16].

2.2. sRNAs Regulate Adhesion to and Invasion of Non-Phagocytic Cells

Salmonella initiates infection of the host by attaching to the intestinal mucosal surface and subsequently adhering to and invading non-phagocytic cells. Adhesion to and invasion of host cells are crucial steps in Salmonella infection. Many adhesive structures such as fimbrial and non-fimbrial proteins were found in Salmonella, including type I fimbriae, autotransporter adhesins, and the outer membrane protein OmpD [1][42][43][44].

2.2.1. sRNAs Regulate the Expression of a Fimbrial Subunit

FimA is the major fimbrial subunit of Type 1 Fimbriae in Salmonella, and it is important for adhesion to enterocytes and colonization of the intestine [18]. STnc640, which is an Hfq-binding sRNA identified in S. Typhimurium by deep sequencing [45], is also present in S. Enteritidis and upregulates the expression of fimA. Although STnc640 regulates the expression of fimA, it decreases the adhesion ability of S. Enteritidis to human colorectal adenocarcinoma epithelial cells (Caco-2) and attenuates the virulence of S. Enteritidis in chickens [19]. STnc150, another sRNA of S. Typhimurium, downregulates the protein expression of FimA by base-pairing with the 5’-end of fimA mRNA. Deletion of STnc150 enhanced the adhesion ability of S. Typhimurium to macrophages and reduced LD50 in mice [46].

2.3. sRNAs Regulate Resistance to Oxidative Stress within Cells

After entry into phagocytic cells, Salmonella faces oxidative stress in the cytoplasm. Phagocytic cells have two important antimicrobial systems, the NADPH phagocyte oxidase (phox) and inducible nitric oxide synthase (iNOS) pathways, which produce ROS and RNS, respectively. ROS play important roles in the early host response to infection, and RNS limit bacterial survival in host cells [47]. As a result, the ability of bacteria to survive the oxidative stress inside hosts is the key to induce pathogenicity. Interestingly, bacteria have involved mature mechanisms to promote survival and replication inside host cells. Recently, sRNAs in Salmonella have been demonstrated to have irreplaceable functions in resisting oxidative stress inside host cells. S. Enteritidis strain SE2472 can use mammalian atypical miRNA processing machinery to cleave sRNA into a ~22-nt miRNA-like RNA fragment, Sal-1, which facilitates the intracellular survival of invaded bacteria by targeting cellular iNOS, attenuating the iNOS-mediated antimicrobial ability of human colonic epithelial cells. sRNAs are important in the resistance to oxidative stress inside host cells [28].
OxyS is a stable and abundant sRNA that was first identified in E. coli. It has been proven that OxyS helps bacteria adapt to the mutagenic effects of hydrogen peroxide (H2O2) and protects E. coli against oxidative damage [48][49]. Moreover, OxyS is strongly activated when S. Typhimurium resides within J774 macrophages, suggesting that SPI-encoded sRNAs play significant roles in the network that regulates the stress response within the macrophage environment [23]. A recent report showed that OxyS could positively regulate the mRNA levels of the porin-encoding gene ompX under H2O2-induced stress in S. Typhimurium, and sRNAs CyaR and MicA positively regulate ompA mRNA levels under H2O2-induced stress [29]. To sum up, OxyS provides important assistance for bacteria to resist oxidative stress.
Some sRNAs also target virulence genes under oxidative stress to promote survival and replication in macrophages. RaoN is a sRNA encoded in the cspH-envE intergenic region on SPI-11. The expression of RaoN is increased under oxidative stress with nutrient-limiting conditions in vitro. It has been shown that the lactate dehydrogenase gene ldhA, whose inactivation and overexpression both render Salmonella more sensitive to oxidative stress, was upregulated in the raoN knockout mutant. Deletion of raoN impedes Salmonella survival and replication in macrophages [30][33].
RyhB and its homologs are key regulators of iron homeostasis in E. coli and Salmonella [31][50]. As an iron-regulatory sRNA, RyhB downregulates a large number of transcripts encoding iron-using proteins when facing iron deficiency and modulates the usage of intracellular iron. Beyond that, RyhB-1 and RyhB-2 expression is induced upon exposure to H2O2 [23]. RyhB deletion mutants (ΔryhB-1, ΔryhB-2, and ΔryhB-1/ΔryhB-2) displayed increased levels of intracellular ROS and a growth defect when treated with H2O2 in iron-rich or iron-deficient conditions. OxyR upregulated the expression of ryhB-1 and ryhB-2 through direct interaction with their promoter region when Salmonella was treated with H2O2 [51]. The above illustrates that RyhB-1 and RyhB-2 are necessary for Salmonella to resist oxidative stress in the intracellular environment.

2.4. sRNAs Regulate Survival in Macrophages

Though T3SS-1 effectors are translocated into host cells to promote invasion of diverse cell types, the expression of T3SS-2 (encoded by SPI-2) is mainly triggered after entering cells and results in translocation of effectors to manipulate the intracellular niche [44][52]. Salmonella suffers extreme stresses in macrophages because macrophages produce RNS and ROS to kill it [4]. Therefore, survival and replication of Salmonella within macrophages is essential for its pathogenicity in hosts. Recently, many sRNAs have been found to promote survival and replication of Salmonella in macrophages.
When Salmonella is present in the intracellular environment of macrophages, the expression of many sRNAs is induced. Transcriptome analysis of intra-macrophage S. Typhimurium showed that 88% of 280 sRNAs were expressed [53]. Compared to the early stationary phase (ESP) conditions, with high expression of SPI-1 genes, 34 sRNAs (including RyhB-1, RyhB-2, OxyS, MicF, and RybB) were upregulated, and 119 sRNAs were downregulated [52]. The expression of many SPI-encoded sRNAs is induced when Salmonella multiplies within macrophages. For example, the transcription of IsrC and IsrN is increased 7-fold within the first hour post-infection of J774 macrophages and declines as infection progresses. IsrC overlaps with its flanking gene msgA at the 3’-end and affects the expression of msgA (encoding a macrophage survival-related protein) in cis. This indicates that IsrC is important for Salmonella to survive in macrophages [23]. OxyS, an sRNA that responds to oxidative stress, shows the same expression pattern as IsrC and IsrN. OxyS levels increase 35-fold within the first hour of infection and decrease thereafter. OxyS is strongly activated by H2O2 and increases the H2O2 resistance of Salmonella in macrophages [23]. The transcript levels of IsrH, IsrE (RyhB-2), and its homolog RyhB-1 increase within the first hour of infection and then increase dramatically at 8 h post-infection. The induction of expression of these sRNAs suggests that these sRNAs play important roles in the survival and replication of Salmonella inside macrophages [23].
Besides regulating the invasion of epithelial cells and the response to oxidative stress, RyhB-1 and RyhB-2 also contribute to intracellular survival in macrophages. In S. Typhi, RyhBs (RfrA and RfrB) are regulated by the ferric uptake regulator (Fur). Expression of both is induced within the human monocyte cell line THP-1 at 24 h post-infection. They are crucial for Salmonella replication inside macrophages [31]. In S. Typhimurium, RyhB-1 and RyhB-2 are the most highly induced sRNAs within macrophages compared to ESP conditions [53]. They contribute to survival and proliferation inside RAW264.7 murine macrophages [32]. Deletion of RyhB-1 and RyhB-2 leads to an increase in ATP levels and a decrease in the NAD+/NADH ratio, resulting in more active metabolism of S. Typhimurium in macrophages. RyhB-1 and RyhB-2 affect the expression of SPI-1-related genes encoding the transcriptional regulators HilA, HilC, HilD, InvF, and RtsA, the effector proteins SipA, SipB, SopA, and SopB, and the tricarboxylic acid cycle-related genes fumA and sdhD, which encode iron-containing enzymes involved in energy metabolism within macrophages. Moreover, RyhB-1 and RyhB-2 directly downregulate the expression of rtsB (encoding an invasion chaperone) and sicA (encoding a regulatory protein). This suggests that the two sRNAs possess the ability to integrate a global response to multiple stresses encountered inside macrophages [32].

2.5. sRNAs Regulate the Expression of Inflammatory Cytokines in Host Cells

The innate immune system is essential to defend against bacterial pathogens [54]. SCVs induce the innate immune response through the interaction of pathogen-associated molecular patterns with Toll-like receptors in host cells, such as epithelial cells and macrophages. Upon this interaction, mitogen-activated protein kinases produce a signal, leading to secretion of a variety of cytokines, such as tumor necrosis factor and interleukin-8 (IL-8), which stimulate antibacterial responses and are beneficial for bacterial clearance [14][55][56]. However, Salmonella has evolved sophisticated methods to modify the host cells to meet their needs by regulating these inflammatory cytokines. This regulatory function of sRNAs of Salmonella has received increasing attention in recent years.

References

  1. Rehman, T.; Yin, L.; Latif, M.B.; Chen, J.H.; Wang, K.Y.; Geng, Y.; Huang, X.L.; Abaidullah, M.; Guo, H.R.; Ouyang, P. Adhesive mechanism of different Salmonella fimbrial adhesins. Microb. Pathog. 2019, 137, 103748.
  2. Jones, B.D.; Ghori, N.; Falkow, S. Salmonella typhimurium initiates murine infection by penetrating and destroying the specialized epithelial M cells of the Peyer’s patches. J. Exp. Med. 1994, 180, 15–23.
  3. Bakowski, M.A.; Braun, V.; Brumell, J.H. Salmonella-containing vacuoles: Directing traffic and nesting to grow. Traffic 2008, 9, 2022–2031.
  4. Fang, F.C. Antimicrobial reactive oxygen and nitrogen species: Concepts and controversies. Nat. Rev. Microbiol. 2004, 2, 820–832.
  5. Waters, L.S.; Storz, G. Regulatory RNAs in bacteria. Cell 2009, 136, 615–628.
  6. Chan, H.; Ho, J.; Liu, X.; Zhang, L.; Wong, S.H.; Chan, M.T.; Wu, W.K. Potential and use of bacterial small RNAs to combat drug resistance: A systematic review. Infect. Drug Resist. 2017, 10, 521–532.
  7. Kwenda, S.; Gorshkov, V.; Ramesh, A.M.; Naidoo, S.; Rubagotti, E.; Birch, P.R.; Moleleki, L.N. Discovery and profiling of small RNAs responsive to stress conditions in the plant pathogen Pectobacterium atrosepticum. BMC Genom. 2016, 17, 47.
  8. Altuvia, S.; Wagner, E.G. Switching on and off with RNA. Proc. Natl. Acad. Sci. USA 2000, 97, 9824–9826.
  9. Chao, Y.; Vogel, J. The role of Hfq in bacterial pathogens. Curr. Opin. Microbiol. 2010, 13, 24–33.
  10. Hoe, C.H.; Raabe, C.A.; Rozhdestvensky, T.S.; Tang, T.H. Bacterial sRNAs: Regulation in stress. Int. J. Med. Microbiol. 2013, 303, 217–229.
  11. Papenfort, K.; Vogel, J. Regulatory RNA in bacterial pathogens. Cell Host Microbe 2010, 8, 116–127.
  12. Masse, E.; Salvail, H.; Desnoyers, G.; Arguin, M. Small RNAs controlling iron metabolism. Curr. Opin. Microbiol. 2007, 10, 140–145.
  13. Rychlik, I.; Barrow, P.A. Salmonella stress management and its relevance to behaviour during intestinal colonisation and infection. FEMS Microbiol. Rev. 2005, 29, 1021–1040.
  14. Ahmed, W.; Zheng, K.; Liu, Z.F. Small non-coding RNAs: New insights in modulation of host immune response by intracellular bacterial pathogens. Front. Immunol. 2016, 7, 431.
  15. Majdalani, N.; Cunning, C.; Sledjeski, D.; Elliott, T.; Gottesman, S. DsrA RNA regulates translation of RpoS message by an anti- antisense mechanism, independent of its action as an antisilencer of transcription. Proc. Natl. Acad. Sci. USA 1998, 95, 12462–12467.
  16. Ryan, D.; Mukherjee, M.; Nayak, R.; Dutta, R.; Suar, M. Biological and regulatory roles of acid-induced small RNA RyeC in Salmonella Typhimurium. Biochimie 2018, 150, 48–56.
  17. Ren, J.; Sang, Y.; Qin, R.; Cui, Z.; Yao, Y.F. 6S RNA is involved in acid resistance and invasion of epithelial cells in Salmonella enterica serovar Typhimurium. Future Microbiol. 2017, 12, 1045–1057.
  18. Althouse, C.; Patterson, S.; Fedorka-Cray, P.; Isaacson, R.E. Type 1 fimbriae of Salmonella enterica serovar Typhimurium bind to enterocytes and contribute to colonization of swine in vivo. Infect. Immun. 2003, 71, 6446–6452.
  19. Meng, X.; Meng, X.C.; Wang, J.Q.; Wang, H.; Zhu, C.H.; Ni, J.; Zhu, G.Q. Small non-coding RNA STnc640 regulates expression of fimA fimbrial gene and virulence of Salmonella enterica serovar Enteritidis. BMC Vet. Res. 2019, 15, 319.
  20. Chen, S.; Zhang, A.; Blyn, L.B.; Storz, G. MicC, a second small-RNA regulator of Omp protein expression in Escherichia coli. J. Bacteriol. 2004, 186, 6689–6697.
  21. Pfeiffer, V.; Papenfort, K.; Lucchini, S.; Hinton, J.C.; Vogel, J. Coding sequence targeting by MicC RNA reveals bacterial mRNA silencing downstream of translational initiation. Nat. Struct. Mol. Biol. 2009, 16, 840–846.
  22. Pfeiffer, V.; Sittka, A.; Tomer, R.; Tedin, K.; Brinkmann, V.; Vogel, J. A small non-coding RNA of the invasion gene island (SPI-1) represses outer membrane protein synthesis from the Salmonella core genome. Mol. Microbiol. 2007, 66, 1174–1191.
  23. Padalon-Brauch, G.; Hershberg, R.; Elgrably-Weiss, M.; Baruch, K.; Rosenshine, I.; Margalit, H.; Altuvia, S. Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulence. Nucleic Acids Res. 2008, 36, 1913–1927.
  24. Gong, H.; Vu, G.P.; Bai, Y.; Chan, E.; Wu, R.; Yang, E.; Liu, F.Y.; Lu, S.W. A Salmonella small non-coding RNA facilitates bacterial invasion and intracellular replication by modulating the expression of virulence factors. PLoS Pathog. 2011, 7, e1002120.
  25. Chen, B.J.; Meng, X.; Ni, J.; He, M.P.; Chen, Y.F.; Xia, P.P.; Wang, H.; Liu, S.G.; Zhu, G.Q. Positive regulation of type III secretion effectors and virulence by RyhB paralogs in Salmonella enterica serovar Enteritidis. Vet. Res. 2021, 52, 44.
  26. Wang, L.; Cai, X.; Wu, S.Y.; Bomjan, R.; Nakayasu, E.S.; Handler, K.; Hinton, J.C.D.; Zhou, D.G. InvS coordinates expression of PrgH and FimZ and is required for invasion of epithelial cells by Salmonella enterica serovar Typhimurium. J. Bacteriol. 2017, 199, e00824-16.
  27. Kim, K.; Palmer, A.D.; Vanderpool, C.K.; Slauch, J.M. The small RNA PinT contributes to PhoP-mediated regulation of the Salmonella pathogenicity island 1 type III secretion system in Salmonella enterica serovar Typhimurium. J. Bacteriol. 2019, 201, e00312-19.
  28. Zhao, C.H.; Zhou, Z.; Zhang, T.F.; Liu, F.Y.; Zhang, C.Y.; Zen, K.; Gu, H.W. Salmonella small RNA fragment Sal-1 facilitates bacterial survival in infected cells via suppressing iNOS induction in a microRNA manner. Sci. Rep. 2017, 7, 16979.
  29. Briones, A.C.; Lorca, D.; Cofre, A.; Cabezas, C.E.; Kruger, G.I.; Pardo-Este, C.; Baquedano, M.S.; Salinas, C.R.; Espinoza, M.; Castro-Severyn, J.; et al. Genetic regulation of the ompX porin of Salmonella Typhimurium in response to hydrogen peroxide stress. Biol. Res. 2022, 55, 8.
  30. Kim, S.; Lee, Y.H. Impact of small RNA RaoN on nitrosative-oxidative stress resistance and virulence of Salmonella enterica serovar Typhimurium. J. Microbiol. 2020, 58, 499–506.
  31. Leclerc, J.M.; Dozois, C.M.; Daigle, F. Role of the Salmonella enterica serovar Typhi Fur regulator and small RNAs RfrA and RfrB in iron homeostasis and interaction with host cells. Microbiology 2013, 159, 91–602.
  32. Penaloza, D.; Acuna, L.G.; Barros, M.J.; Nunez, P.; Montt, F.; Gil, F.; Fuentes, J.A.; Calderon, I.L. The small RNA RyhB homologs from Salmonella Typhimurium restrain the intracellular growth and modulate the SPI-1 gene expression within RAW264.7 macrophages. Microorganisms 2021, 9, 635.
  33. Lee, Y.H.; Kim, S.; Helmann, J.D.; Kim, B.H.; Park, Y.K. RaoN, a small RNA encoded within Salmonella pathogenicity island-11, confers resistance to macrophage-induced stress. Microbiology 2013, 159, 1366–1378.
  34. Westermann, A.J.; Forstner, K.U.; Amman, F.; Barquist, L.; Chao, Y.; Schulte, L.N.; Muller, L.; Reinhardt, R.; Stadler, P.F.; Vogel, J. Dual RNA-seq unveils noncoding RNA functions in host-pathogen interactions. Nature 2016, 529, 496–501.
  35. Correia Santos, S.; Bischler, T.; Westermann, A.J.; Vogel, J. MAPS integrates regulation of actin-targeting effector SteC into the virulence control network of Salmonella small RNA PinT. Cell Rep. 2021, 34, 108722.
  36. Foster, J.W.; Hall, H.K. Adaptive acidification tolerance response of Salmonella typhimurium. J. Bacteriol. 1990, 172, 771–778.
  37. Chen, C.Y.; Eckmann, L.; Libby, S.J.; Fang, F.C.; Okamoto, S.; Kagnoff, M.F.; Fierer, J.; Guiney, D.G. Expression of Salmonella typhimurium rpoS and rpoS-dependent genes in the intracellular environment of eukaryotic cells. Infect. Immun. 1996, 64, 4739–4743.
  38. Ryan, D.; Ojha, U.K.; Jaiswal, S. The small RNA DsrA influences the acid tolerance response and virulence of Salmonella enterica serovar Typhimurium. Front. Microbiol. 2016, 7, 599.
  39. Sledjeski, D.D.; Gupta, A.; Gottesman, S. The small RNA, DsrA, is essential for the low temperature expression of RpoS during exponential growth in Escherichia coli. EMBO J. 1996, 15, 3993–4000.
  40. Lease, R.A.; Smith, D.; McDonough, K.; Belfort, M. The small noncoding DsrA RNA is an acid resistance regulator in Escherichia coli. J. Bacteriol. 2004, 186, 6179–6185.
  41. Fozo, E.M.; Kawano, M.; Fontaine, F.; Kaya, Y.; Mendieta, K.S.; Jones, K.L.; Ocampo, A.; Rudd, K.E.; Storz, G. Repression of small toxic protein synthesis by the Sib and OhsC small RNAs. Mol. Microbiol. 2008, 70, 1076–1093.
  42. Wagner, C.; Hensel, M. Adhesive mechanisms of Salmonella enterica. Adv. Exp. Med. Biol. 2011, 715, 17–34.
  43. Hara-Kaonga, B.; Pistole, T.G. OmpD but not OmpC is involved in adherence of Salmonella enterica serovar typhimurium to human cells. Can. J. Microbiol. 2004, 50, 719–727.
  44. Hensel, M. Evolution of pathogenicity islands of Salmonella enterica. Int. J. Med. Microbiol. 2004, 294, 95–102.
  45. Sittka, A.; Lucchini, S.; Papenfort, K.; Sharma, C.M.; Rolle, K.; Binnewies, T.T.; Hinton, J.C.; Vogel, J. Deep sequencing analysis of small noncoding RNA and mRNA targets of the global post-transcriptional regulator, Hfq. PLoS Genet. 2008, 4, e1000163.
  46. Li, J.; Li, N.; Ning, C.C.; Guo, Y.; Ji, C.H.; Zhu, X.Z.; Zhang, X.X.; Meng, Q.L.; Shang, Y.X.; Xiao, C.C.; et al. sRNA STnc150 is involved in virulence regulation of Salmonella Typhimurium by targeting fimA mRNA. FEMS Microbiol. Lett. 2021, 368, fnab124.
  47. Mastroeni, P.; Vazquez-Torres, A.; Fang, F.C.; Xu, Y.; Khan, S.; Hormaeche, C.E.; Dougan, G. Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. II. Effects on microbial proliferation and host survival in vivo. J. Exp. Med. 2000, 192, 237–248.
  48. Altuvia, S.; Weinstein-Fischer, D.; Zhang, A.; Postow, L.; Storz, G. A small, stable RNA induced by oxidative stress: Role as a pleiotropic regulator and antimutator. Cell 1997, 90, 43–53.
  49. Schlosser-Silverman, E.; Elgrably-Weiss, M.; Rosenshine, I.; Kohen, R.; Altuvia, S. Characterization of Escherichia coli DNA lesions generated within J774 macrophages. J. Bacteriol. 2000, 182, 5225–5230.
  50. Massé, E.; Gottesman, S. A small RNA regulates the expression of genes involved in iron metabolism in Escherichia coli. Proc. Natl. Acad. Sci. USA 2002, 99, 4620–4625.
  51. Calderon, I.L.; Morales, E.H.; Collao, B.; Calderon, P.F.; Chahuan, C.A.; Acuna, L.G.; Gil, F.; Saavedra, C.P. Role of Salmonella Typhimurium small RNAs RyhB-1 and RyhB-2 in the oxidative stress response. Res. Microbiol. 2014, 165, 30–40.
  52. Steele-Mortimer, O.; Brumell, J.H.; Knodler, L.A.; Méresse, S.; Lopez, A.; Finlay, B.B. The invasion-associated type III secretion system of Salmonella enterica serovar typhimurium is necessary for intracellular proliferation and vacuole biogenesis in epithelial cells. Cell Microbiol. 2002, 4, 43–54.
  53. Srikumar, S.; Kröger, C.; Hébrard, M.; Colgan, A.; Owen, S.V.; Sivasankaran, S.K.; Cameron, A.D.; Hokamp, K.; Hinton, J.C. RNA-seq brings new insights to the intra-macrophage transcriptome of Salmonella Typhimurium. PLoS Pathog. 2015, 11, e1005262.
  54. Medzhitov, R. Recognition of microorganisms and activation of the immune response. Nature 2007, 449, 819–826.
  55. Zhong, J.; Kyriakis, J.M. Dissection of a signaling pathway by which pathogen-associated molecular patterns recruit the JNK and p38 MAPKs and trigger cytokine release. J. Biol. Chem. 2007, 282, 24246–24254.
  56. Bahrami, B.; Macfarlane, S.; Macfarlane, G.T. Induction of cytokine formation by human intestinal bacteria in gut epithelial cell lines. J. Appl. Microbiol. 2011, 110, 353–363.
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Subjects: Agriculture, Dairy & Animal Science
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Xia Meng
,
Mengping He
,
Pengpeng Xia
,
Jinqiu Wang
,
Heng Wang
,
Guoqiang Zhu
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Revisions: 2 times (View History)
Update Date: 19 Sep 2022
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