J Pediatr Infect Dis 2021; 16(03): 106-110
DOI: 10.1055/s-0041-1724021
Original Article

Expression of MicroRNA of Macrophages Infected with Attenuated Leishmania major Parasite

Mohammad Hossein Feiz Haddad
1   Cellular and Molecular Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
2   Department of Parasitology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
,
Hossein Rezvan
3   Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran
,
Alireza Nourian
3   Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran
,
Habib Habibpour
1   Cellular and Molecular Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
2   Department of Parasitology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
› Author Affiliations
Funding This study received financial support from Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran (grant No. CMRC-9820).

Abstract

Objective Leishmaniasis has been proposed as one of the neglected vector-borne diseases due to an obligate intracellular parasite of the genus Leishmania. MicroRNAs (miRNAs) with a length of 22-nucleotide are known as the noncoding small RNAs. MiRNAs contribute to many biological and cellular approaches. Therefore, the present study evaluated expressing mmu-miR-721, mmu-miR-294–3p, mmu-miR-155–3p, and mmu-miR-30a in murine macrophages infected with attenuated Leishmania major parasites on 3 days after infection.

Methods Attenuated promastigotes have been achieved after 20 passages of Leishmania major parasites. Cell line J774A.1 (murine macrophage) has been used for in vitro experiments. The stationary phase of attenuated L. major promastigotes has been chosen to infect the cells, and then their incubation has been performed with 5% CO2 at 37°C for 3 days. The real-time polymerase chain reaction (PCR) has also been performed with SYBR Green master-mix Kit for measuring the level of mmu-miR-721, mmu-miR-294–3p, mmu-miR-30a, and mmu-miR-155-3p expression. Uninfected macrophages have been considered as a control group.

Results Real-time PCR demonstrated overexpression of mmu-miR-155-3p, mmu-miR-294–3p, and, mmu-miR-721 in the infected cells with Leishmania parasites after 3 days. Results showed no statistically significant difference in the mmu-miR-30a expression between infected macrophages and the uninfected control group.

Conclusion Our findings suggested the significant contribution of the alterations in the miRNA levels to the regulation of macrophage functions following the creation of intracellular parasites like Leishmania. These data could help to understand better the genes' expression in the host cells in the course of leishmaniasis.

Declaration

The manuscript is the original work of authors.


All data, tables, etc., used in the manuscript are prepared originally by authors, otherwise the sources are cited and reprint permission is attached.


The manuscript has not been and will not be published elsewhere or submitted elsewhere for publication.


Ethical Approval

The study protocol is done based on the Helsinki declaration and was confirmed by the ethics committee of the deputy of research of Ahvaz Jundishapour University of Medical Sciences, Ahvaz, Iran (grant no.: IR.AJUMS.ABHC.REC.1398.074).




Publication History

Received: 03 September 2020

Accepted: 22 December 2020

Article published online:
25 February 2021

© 2021. Thieme. All rights reserved.

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  • References

  • 1 Hamoon Navard S, Rezvan H, Feiz Haddad MH. et al. Therapeutic effects of mesenchymal stem cells on cutaneous leishmaniasis lesions caused by Leishmania major . J Glob Antimicrob Resist 2020; 23: 243-250
  • 2 McGwire BS, Satoskar AR. Leishmaniasis: clinical syndromes and treatment. QJM 2014; 107 (01) 7-14
  • 3 Feiz-Haddad MH, Safaei K, Saki A, Feiz-Haddad R. Epidemiological study of cutaneous leishmaniasis in southwest of Iran during 2001–2011. Asian Pac J Trop Dis 2016; 6 (06) 432-436
  • 4 Shokri A, Emami S, Fakhar M, Teshnizi SH, Keighobadi M. In vitro antileishmanial activity of novel azoles (3-imidazolylflavanones) against promastigote and amastigote stages of Leishmania major . Acta Trop 2017; 167: 73-78
  • 5 Patwardhan V, Kumar D, Singh S. Parasitic infections in pediatric population of india: epidemiology, diagnosis, and strategies for prevention. J Pediatr Infect Dis 2017; 12 (04) 228-237
  • 6 Rezvan H, Moafi M. An overview on Leishmania vaccines: a narrative review article. Vet Res Forum 2015; 6 (01) 1-7
  • 7 Liu D, Uzonna JE. The early interaction of Leishmania with macrophages and dendritic cells and its influence on the host immune response. Front Cell Infect Microbiol 2012; 2: 83
  • 8 Merida-de-Barros DA, Chaves SP, Belmiro CLR, Wanderley JLM. Leishmaniasis and glycosaminoglycans: a future therapeutic strategy?. Parasit Vectors 2018; 11 (01) 536
  • 9 Rossi M, Fasel N. How to master the host immune system? Leishmania parasites have the solutions!. Int Immunol 2018; 30 (03) 103-111
  • 10 Gupta AK, Singh A, Srivastava S, Shankar P, Singh S. Visceral leishmaniasis in children: diagnosis, treatment, and prevention. J Pediatr Infect Dis 2017; 12 (04) 214-221
  • 11 Nawaz M. Nanotechnology-based approaches in pediatric parasitic infections. J Pediatr Infect Dis 2017; 12 (04) 264-270
  • 12 Shokri A, Saeedi M, Fakhar M. et al. Antileishmanial activity of Lavandula angustifolia and Rosmarinus officinalis essential oils and nano-emulsions on Leishmania major (MRHO/IR/75/ER). Iran J Parasitol 2017; 12 (04) 622-631
  • 13 Liu Q, Tuo W, Gao H, Zhu X-Q. MicroRNAs of parasites: current status and future perspectives. Parasitol Res 2010; 107 (03) 501-507
  • 14 Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell 2009; 136 (02) 215-233
  • 15 Rodriguez A, Vigorito E, Clare S. et al. Requirement of bic/microRNA-155 for normal immune function. Science 2007; 316 (5824): 608-611
  • 16 Trotta R, Chen L, Ciarlariello D. et al. miR-155 regulates IFN-γ production in natural killer cells. Blood 2012; 119 (15) 3478-3485
  • 17 Eren RO, Reverte M, Rossi M. et al. Mammalian innate immune response to a Leishmania-resident RNA virus increases macrophage survival to promote parasite persistence. Cell Host Microbe 2016; 20 (03) 318-328
  • 18 Tili E, Michaille J-J, Cimino A. et al. Modulation of miR-155 and miR-125b levels following lipopolysaccharide/TNF-α stimulation and their possible roles in regulating the response to endotoxin shock. J Immunol 2007; 179 (08) 5082-5089
  • 19 Singh AK, Pandey RK, Shaha C, Madhubala R. MicroRNA expression profiling of Leishmania donovani-infected host cells uncovers the regulatory role of MIR30A-3p in host autophagy. Autophagy 2016; 12 (10) 1817-1831
  • 20 Zhu H, Wu H, Liu X. et al. Regulation of autophagy by a beclin 1-targeted microRNA, miR-30a, in cancer cells. Autophagy 2009; 5 (06) 816-823
  • 21 Chen Z, Wang T, Liu Z. et al. Inhibition of autophagy by MiR-30A induced by mycobacteria tuberculosis as a possible mechanism of immune escape in human macrophages. Jpn J Infect Dis 2015; 68 (05) 420-424
  • 22 Frank B, Marcu A, de Oliveira Almeida Petersen AL. et al. Autophagic digestion of Leishmania major by host macrophages is associated with differential expression of BNIP3, CTSE, and the miRNAs miR-101c, miR-129, and miR-210. Parasit Vectors 2015; 8: 404-404
  • 23 Lemaire J, Mkannez G, Guerfali FZ. et al; Sysco-Consortium. MicroRNA expression profile in human macrophages in response to Leishmania major infection. PLoS Negl Trop Dis 2013; 7 (10) e2478
  • 24 Ghosh J, Bose M, Roy S, Bhattacharyya SN. Leishmania donovani targets Dicer1 to downregulate miR-122, lower serum cholesterol, and facilitate murine liver infection. Cell Host Microbe 2013; 13 (03) 277-288
  • 25 Geraci NS, Tan JC, McDowell MA. Characterization of microRNA expression profiles in Leishmania-infected human phagocytes. Parasite Immunol 2015; 37 (01) 43-51
  • 26 Muxel SM, Laranjeira-Silva MF, Zampieri RA, Floeter-Winter LM. Leishmania (Leishmania) amazonensis induces macrophage miR-294 and miR-721 expression and modulates infection by targeting NOS2 and L-arginine metabolism. Sci Rep 2017; 7: 44141
  • 27 Ali KS, Rees RC, Terrell-Nield C, Ali SA. Virulence loss and amastigote transformation failure determine host cell responses to Leishmania mexicana . Parasite Immunol 2013; 35 (12) 441-456
  • 28 Moreira D, Santarém N, Loureiro I. et al. Impact of continuous axenic cultivation in Leishmania infantum virulence. PLoS Negl Trop Dis 2012; 6 (01) e1469
  • 29 Noorpisheh Ghadimi S, Homayoon L, Shahriarirad R, Fatehpour S, Rastegarian M, Sarkari B. Attenuated Leishmania major induce a high level of protection against Leishmania infantum in BALB/c mice. Iran J Parasitol 2019; 14 (02) 310-317
  • 30 Hashemi N, Sharifi M, Tolouei S, Hashemi M, Hashemi C, Hejazi SH. Expression of hsa Let-7a MicroRNA of macrophages infected by Leishmania major . Int J Med Res Health Sci 2018; 5 (10) 27-32
  • 31 Hsu Y-A, Lin C-H, Lin H-J. et al. Effect of microRNA-155 on the interferon-gamma signaling pathway in biliary atresia. Chin J Physiol 2016; 59 (06) 315-322
  • 32 Manzano-Román R, Siles-Lucas M. MicroRNAs in parasitic diseases: potential for diagnosis and targeting. Mol Biochem Parasitol 2012; 186 (02) 81-86
  • 33 Lodish HF, Zhou B, Liu G, Chen C-Z. Micromanagement of the immune system by microRNAs. Nat Rev Immunol 2008; 8 (02) 120-130
  • 34 Rodriguez NE, Chang HK, Wilson ME. Novel program of macrophage gene expression induced by phagocytosis of Leishmania chagasi . Infect Immun 2004; 72 (04) 2111-2122
  • 35 Lin Y, Sibanda VL, Zhang H-M, Hu H, Liu H, Guo A-Y. MiRNA and TF co-regulatory network analysis for the pathology and recurrence of myocardial infarction. Sci Rep 2015; 5: 9653
  • 36 Qin Y, Wang Q, Zhou Y, Duan Y, Gao Q. Inhibition of IFN-γ-induced nitric oxide dependent antimycobacterial activity by miR-155 and C/EBPβ. Int J Mol Sci 2016; 17 (04) 535
  • 37 Silva SC, Silva DF, Almeida TC. et al. Behavior of two Leishmania infantum strains-evaluation of susceptibility to antimonials and expression of microRNAs in experimentally infected J774 macrophages and in BALB/c mice. Parasitol Res 2018; 117 (09) 2881-2893
  • 38 Wendlandt EB. Macrophage microRNA and mRNA responses to stimulation of TLRs or upon infection with Leishmania infantum chagasi [dissertation]. Iowa, Missouri: University of Iowa; 2013