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Diseases 2019, 7(1), 9; https://doi.org/10.3390/diseases7010009

Review
The MAPK Signaling Pathways as a Novel Way in Regulation and Treatment of Parasitic Diseases
Department of Nursing Teaching and Research, School of Basic Medicine, Guilin Medical University, Guilin 541004, China
*
Author to whom correspondence should be addressed.
Received: 3 December 2018 / Accepted: 15 January 2019 / Published: 17 January 2019

Abstract

:
Few major advances in fighting parasitic diseases have been made in China since the development of new methods for prevention, control, and elimination. However, the proportion of immunocompromised individuals has increased due to the growth of chronic diseases, population aging, and more frequent cases of patients with AIDS and cancer. All these problems can promote development of parasitic infections, which is commonly associated with manipulation of host signaling pathways and the innate immune system. Mitogen-activated protein kinase (MAPK) signaling pathways are evolutionarily conserved in metazoan organisms, which play critical roles in the cell cycle, gene expression, growth, differentiation, apoptosis, and parasite–host interactions. Recent discoveries of the MAPK components involved in activation, regulation, and signal transduction appeared to be promising for the diagnosis, prevention, and treatment of parasitic diseases in the future. This review summarizes the involvement and critical role of the MAPK family in parasitic disease development and maintenance in the host. Moreover, it highlights recent studies concerning the mechanisms and novel drug development for inhibition and regulation of MAPK pathways in order to prevent parasitic disease. In addition, we discuss some antigenic proteins as prospective inhibitory molecules or vaccines for the regulation and control of MAPK signaling involved in parasite physiological activity.
Keywords:
MAPK; mitogen-activated protein kinase; transduction pathway; parasite

1. Introduction

Significant advances have been made in the control and elimination of human parasitic diseases in China since the growth of central and local government attention in developing a range of control programs, as well as improvements in hygienic conditions. Therefore, recent improvements resulted in significant decrease of clinical incidents associated with the hookworms, roundworms, and other soil-transmitted infections. However, the increased prevalence of foodborne parasitic diseases in some provinces of China remains a challenging issue. For instance, the abundance of hydatidosis is still a serious problem in Western China [1]. Furthermore, the growing number of people in the older generation and the increase of chronic diseases resulted in an increase in the number of immunocompromised individuals in the population, which also includes frequent cases of patients with AIDS or cancer [2]. Therefore, the acute problem of parasitic infections is one of the major subjects for health protection and research in China.
Many pathogens target a variety of cell signaling pathways to inhibit or modulate the host’s immune response [3]. Besides strategies to overcome the immune response, pathogens can also utilize cell signaling, including the mitogen-activated protein kinase (MAPK), for the most appropriate cellular response [4].
MAPK signaling includes many evolutionary conserved pathways, which are essential in virtually all metazoan organisms [5]. MAPK signal transduction molecules can modulate a variety of crucial functions in both host and parasite cells, such as cell differentiation [6,7], proliferation [8,9], and apoptosis [8,10]. For instance, Erika Pellegrini et al. found that the intracellular parasite Toxoplasma gondii has an ability to deliver a protein, GRA24, into cells, which establishes an interaction with a host protein, p38αMAPK(MAPK14). Consequently this interaction results in activation and nuclear translocation of the host kinase, which triggers an inflammatory response [11]. In addition, MAPK is regulated through the activation of three family members: MAPKKK/MEKK/MKKK, MAPKK/MEK/MKK, and MAPK [5]. Therefore, the MAPK pathway is subdivided into three branches: ERK1/2, JNK1/2/3, and p38 MAPK (Figure 1) [6].
Taking in account an important role of MAPK in cell proliferation and survival, many researches are focused on developing novel drugs for eliminating parasites via a specific inhibition of their MAPK pathway. Moreover, a profound study of the mechanism of function and regulation of MAPK signaling could reveal important findings regarding a molecular mechanism of the host–parasite interaction. Therefore, it can be extensively utilized for diagnostic, treatment, and prevention of parasitic diseases.

2. Research Directions and MAPK Mechanism of Action in Parasitic Diseases

2.1. The MAPK Interplay Between a Parasite and Host

Currently, there are no ideal vaccines or methods for diagnosis or treatment for various parasitic diseases due to the lack of knowledge in molecular levels of manipulated immune response by parasites. Thus, studies are required to increase our understanding of MAPK-dependent mechanisms, which are one of the most important in host–parasite interaction.
Zhang C et al. found that the mechanism of simultaneous activation of cell proliferation and apoptosis in human hepatocytes infected with Echinococcus multilocularis [9]. This mechanism is regulated through the activation of ERK1/2 and downstream molecules at the early stage of infection, which results in proliferation of host hepatocytes. Moreover, the damage caused by parasites and related cytokines do not affect hepatocytes during the continuous activation of the pathway. However, consequent activation of JNK and the expression of some specific molecules trigger a growth arrest and induce apoptosis of hepatocytes (Table 1).
Zhou L. et al. found that Clonorchis sinensis lysophospholipase A (CsLysoPLA) can activate the PKA-dependent B-Raf/ERK1/2 pathway in mouse macrophages [12]. In their study, it was demonstrated that CsLysoPLA triggered upregulation of IL-25 secretion in macrophages through the MAPK pathway. Therefore, IL-25 can activate hepatic stellate cells (HSCs), resulting in enhanced proliferation of hepatic mesenchymal cells and liver fibrosis (Table 1) [12].
ERK1/2 MAPK activation by Trypanosoma cruzi (T. cruzi) associated with cellular proliferation in the BeWo trophoblast cell line was shown by Droguett D et al. (Table 1) [7]. Moreover, Hassan et al. have also demonstrated that T. cruzi can induce proliferation of vascular smooth muscle cells in the myocardium [13]. In addition, it has also been reported by Bouzahzah et al. that promoted proliferation of hepatic cell via altered activation of ERK1/2 MAPK signaling pathway was induced by T. cruzi [14].
Of the most interesting findings about human neutrophils function is a unique form of cell death, netosis, which is associated with granular and cytoplasmic proteins release which entraps and kills microbes. Interestingly, Leishmania amazonensis (L. amazonensis) can release extracellular traps of neutrophils, which lead to elimination of the parasite. The L. amazonensis induced netosis is triggered through the ERK pathway, in which activation takes place downstream of the PI3K cascade independent of AKT and upstream ROS generation (Table 1) [15].
Altogether, Leishmania spp. and T. cruzi use different strategies for a survival in a host cells after infection. For instance, they evolved to target the MAPK signaling pathways and highjack the immune response of a host cell. Moreover, it can target macrophages, and use host molecules to favor infection process and survival inside host cells (Table 1) [16].
A state-of-the-art research conducted by Quan JH et al. provided a new insight on the intracellular networks of the PI3K/AKT and MAPK signaling cascades for regulating T. gondii-induced IL-23 and IL-12 secretion in human monocytic cells (Table 1) [17]. In their work, it was demonstrated that production of IL-23 in T. gondii-infected THP-1 cells was regulated mainly by TLR2 and consequently by PI3K and ERK1/2. However, IL-12 production was mainly regulated by TLR4 and then by p38 MAPK and JNK [17].

2.2. Detection and Prevention of Parasites at MAPK Level

Similar to an antigen, parasites can trigger the immune response of a host. For instance, the cross-linking reaction protein (CRP) of Schistosoma mansoni (S. mansoni), especially in female parasites, can specifically react with an antibody against human ERK kinase [18]. Furthermore, Zhao Quan et al. demonstrated that the recombinant MAPK1 protein of T. gondii can be potentially utilized as a diagnostic antigen [19].
The recombinant proteins of parasites also have biological functions in stimulating cellular and humoral immunity. Therefore, it can be implemented in developing novel ways for enhancing a host’s immune response without causing tissue damage by utilizing replicated parasite genes responsible for the immunogenic products. As an example, ROP18 and TgMAPK1 gene coding proteins can be utilized as a potential vaccine candidate in T. gondii. ROP18 is a newly discovered rhoptry protein with Ser-Thr kinase activity, which is an important regulator of T. gondii proliferation in host cells, as well as a key virulence factor. The ability of ROP18 to regulate host immune-related cytokines and inhibit the transcription of host cells by downregulating the MAPK signaling pathway makes him the most appealing vaccine candidate [20]. For instance, cells infected with a type I T. gondii display overexpression of ROP38, which consequently inhibits the anti-infection-related genes [21]. Moreover, the expression products of MAPK1 and MAPK2, encoded by genes of T. gondii, are closely related to its growth, development, and pathogenicity; they are also considered virulence factors [22]. In addition, bioinformatics analysis of the TgMAPK1 gene structure of T. gondii revealed the specific characteristics of its encoded protein. This protein is characterized as immunogenic, soluble, and with multiple epitopes, which can be potentially utilized as vaccine candidate antigens for toxoplasmosis [23].

2.3. Treatment of MAPK-Dependent Parasitic Diseases

MAPK signaling plays a crucial role in the process of a parasite and host interaction, alongside the invasion step and proliferation of the parasite. For instance, Song Xinshuai et al. demonstrated the importance of MAPK1 in a parasite and host interaction by constructing MAPK1-deficient T. gondii. Therefore, they showed that upon MAPK1 deletion in T. gondii, the levels or adhesion, proliferation, and toxicity were significantly reduced (Table 2) [10].
Various studies have indicated the possibility to reduce invasiveness and pathogenicity of parasites through the interference with their normal activity of MAPK signaling pathway. The study of T. gondii showed that different components of MAPK pathways display a broad spectrum of effects on the differentiation and proliferation of tachyzoites in host cells. Invalidation of corresponding MAPK molecules in the pathway is one of the important factors in order to reduce the invasion efficiency or proliferation rate of tachyzoites [24]. One of the molecules for controlling invasiveness of parasites is PD98059, which is a specific inhibitor of ERK1/2. The inhibitory effect of PD98059 results in a significant reduction of MEK1 activity, leading to poor levels or even termination of invasiveness [25]. Additionally, a variety of studies have shown that MAPK inhibitor U0126 can also significantly inhibit the invasion of T. gondii tachyzoites into host cells by interfering with the sequential release of secretory organelles, such as micronemes, rhoptries, and densegranules [25,26]. Likewise, phospholipaseA2 (PLA2) inhibitors can induce ERK1 or ERK2 to form a dimer, which results in significant reduction of the invasion efficiency of tachyzoites into the host cells. Moreover, a penetration enhancing factor (PEF) also causes obvious changes in the process of tachychite invading host cells. It is noteworthy that U0126 inhibits the cytokines, which is activated by the invasion of T. gondii, and causes a destruction of the balance between the host autoimmune response system and T. gondii. This molecular mechanism of U0126 action leads to inhibition of the T. gondii invasion into the host cells [27].
Unlike T. gondii, low concentrations of p38 inhibitors can effectively inhibit the activity of p38 protein kinase in E. multilocularis and reduce growth and development of the parasite. However, there is no effect on the activity of p38 protein kinase in human cells. EgRAS, EgRAL, and EgP38 genes of Echinococcus granulosus (E. granulosus) are potential drug targets, which can be regulated for a treatment of echinococcosis in order to interfere with growth and invasion of E. granulosus [28]. Both SB202190 and SP600125 inhibitors of p38 and JNK, and can trigger apoptosis of E. granulosus protoscolices in metacestode through inhibition of MAPK signaling pathway in E. granulosus [29].
Chauhan et al. found that DBA (dibenzalacetone) can lead to apoptosis off cells in Leishmania donovani (L. donovani) via the activation of the MAPK cascades (Table 2) [11].
Zhe Cheng et al. [30] found that EGF-mediated EGFR/ERK signaling pathway promotes germinative cell proliferation in E. multilocularis and contributes to larval growth. Targeting the signaling pathways involved in regulating germinative cells may provide a novel therapeutic strategy against echinococcosis and other human cestodiasis (Table 2). In fact, pyridinylimidazoles have already been proved promising compounds with anti-Echinococcus activity by specifically targeting the p38 MAPK family [5].

3. Conclusions

MAPK signaling pathway is a critical mechanism, which is involved in cell growth, proliferation, and differentiation. Numerous studies focusing on gene cloning, sequence analysis, and functional identification of molecules related to MAPK signaling pathway provided a better understanding about the mechanisms involved in the interaction between parasite and host, which cause various pathological processes. These findings provide novel avenues for development of new methods for prevention, diagnosis, treatment, and clinical application against parasitic diseases. Recently, significant progress has been made in the study of MAPK signaling in parasitic diseases. However, further studies are required for better understanding of the signal molecules and mechanism involved in it. Therefore, it has a great potential in control of parasitic diseases, clinical applications including diagnosis, prevention, and treatment.

Funding

This research was funded by Natural Science Foundation of Guangxi Province of China, grant number [GKJZ2016 NO.380].

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lu, Y.; Huang, Q.; Zhou, Z.; Lu, Y. An overview of parasitic diseases by analyzing publications at National Institute of Parasitic Diseases Control and Prevention in the last five years. Chin. J. Dis. Control. Prev. 2015, 19, 86–90. [Google Scholar]
  2. Zhu, H. Research Progress on Opportunistic Parasitic Infections. Chin. J. Parasitol. Parasit. Dis. 2015, 33, 450–455. [Google Scholar]
  3. Roy, C.R.; Mocarski, E.S. Pathogen subversion of cell-intrinsic innate immunity. Nat. Immunol. 2007, 8, 1179–1187. [Google Scholar] [CrossRef]
  4. Han, Z.G.; Brindley, P.J.; Wang, S.Y.; Chen, Z. Schistosoma genomics: New perspectives on schistosome biology and host-parasite interaction. Annu. Rev. Genomics Hum. Genet. 2009, 10, 211–240. [Google Scholar] [CrossRef] [PubMed]
  5. Brehm, K.; Kozio, U. Echinococcuse-Host Interactions at Cellular and Molecular Levels. Adv. Parasit. 2017, 95, 147–212. [Google Scholar] [CrossRef]
  6. Soares-Silva, M.; Diniz, F.F.; Gomes, G.N.; Bahia, D. The Mitogen-Activated Protein Kinase (MAPK) Pathway: Role in Immune Evasion by Trypanosomatids. Front. Microbiol. 2016, 7, 183. [Google Scholar] [CrossRef] [PubMed]
  7. Droguett, D.; Carrillo, I.; Castillo, C.; Gómez, F.; Negrete, M.; Liempi, A.; Muñoz, L.; Galanti, N.; Maya, J.D.; Kemmerling, U. Trypanosoma cruzi induces cellular proliferation in the trophoblastic cell line BeWo. Exp. Parasitol. 2017, 173, 9–17. [Google Scholar] [CrossRef]
  8. Guilherme, R.R.; Monteiro dos, S.; Marcio, F.; Felipe, A.; Pedro, L.O. Functional studies of TcRjl, a novel GTPase of Trypanosoma cruzi, reveals phenotypes related with MAPK activation during parasite differentiation and after heterologous expression in Drosophila model system. Biochem. Biophys. Res. Commun. 2015, 467, 115–120. [Google Scholar] [CrossRef]
  9. Zhang, C.; Wang, J.; Lv, G.; Li, J.; Lu, X.; Mantion, G.; Vuitton, D.A.; Wen, H.; Lin, R. Hepatocyte proliferation/growth arrest balance in the liver of mice during E. multilocularis infection: A coordinated 3-stage course. PLoS ONE 2012, 7, 1–17. [Google Scholar] [CrossRef]
  10. Song, X. Construction and Biological Characteristics of MAPK1-Deficient Toxoplasma gondii. Master’s Thesis, Jilin Agricultural University, Changchun, China, March 2013. [Google Scholar]
  11. Chauhan, I.S.; SubbaRao, G.; Shankar, J.; Chauhan, L.K.S.; Kapadia, G.J.; Singh, N. Chemoprevention of Leishmaniasis: In vitro antiparasitic activity of dibenzalacetone, a synthetic curcumin analog leads to apoptotic cell death in Leishmania donovani. Parasitol. Int. 2018, 67, 627–636. [Google Scholar] [CrossRef]
  12. Zhou, L.; Shi, M.; Zhao, L.; Lin, Z.; Tang, Z.; Sun, H.; Chen, T.; Lv, Z.; Xu, J.; Huang, Y.; et al. Clonorchis sinensis lysophospholipase aupregulates IL-25 expression in macrophages as a potential pathway to liver fibrosis. Parasit. Vectors 2017, 10, 295. [Google Scholar] [CrossRef] [PubMed]
  13. Hassan, G.S.; Mukherjee, S.; Nagajyothi, F.; Louis, M.W.; Stefka, B.P.; Cecilia, J.; Huang, H.; Mahalia, S.D.; Boumediene, B.; Richard, G.P.; et al. Trypanosoma cruzi infection induces proliferation of vascular smooth muscle cells. Infect. Immun. 2006, 74, 152–159. [Google Scholar] [CrossRef] [PubMed]
  14. Bouzahzah, B.; Nagajyothi, F.; Desruisseaux, M.S.; Mohan, K.; Stephen, M.F.; Alex, W.C.; Michael, P.L.; Stefka, B.P.; Richard, G.P.; Murray, W.; et al. Cell cycle regulatory proteins in the liver in murine Trypanosoma cruzi infection. Cell Cycle 2006, 5, 2396–2400. [Google Scholar] [CrossRef] [PubMed]
  15. DeSouza-Vieira, T.; Guimarães-Costa, A.; Rochael, N.C.; Lira, M.N.; Nascimento, M.T.; Lima-Gomez, P.S.; Mariante, R.M.; Persechini, P.M.; Saraiva, E.M. Neutrophil extracellular traps release induced by Leishmania: Role of PI3Kγ, ERK, PI3Kσ, PKC, and [Ca2+]. Leukoc Biol. 2016, 100, 801–810. [Google Scholar] [CrossRef] [PubMed]
  16. Pellegrini, E.; Palencia, A.; Braun, L.; Kapp, U.; Bougdour, A.; Belrhali, H.; Bowler, M.W.; Hakimi, M.A. Structural Basis for the Subversion of MAP Kinase Signaling by an Intrinsically Disordered Parasite Secreted Agonist. Structure 2016, 25, 16–26. [Google Scholar] [CrossRef]
  17. Quan, J.H.; Chu, J.Q.; Kwon, J.; In-Wook, C.; HassanAhmedHassan, A.I.; Wei, Z.; Guang-Ho, C.; Yu, Z.; Jae-Min, Y.; Eun-Kyeong, J.; et al. Intracellular Networks of the PI3K/AKT and MAPK Pathways for Regulating Toxoplasma gondii-Induced IL-23 and IL-12 Production in Human THP-1 Cells. PLoS ONE 2015, 10, 1–22. [Google Scholar] [CrossRef] [PubMed]
  18. Xu, C.; Kong, X. Relationship between MAPK and parasites. Chin. J. Tradit. Vet. Sci. 2015, 9, 46. [Google Scholar]
  19. Gong, S.; Zhao, Q.; Liu, Q. Cloning and Prokaryotic Expression of MAPK1 Gene of Toxoplasma gondii. J. Jilin Agric. Univ. 2015, 37, 221–225, 236. [Google Scholar]
  20. Lucia, P.; Feng, C.; Omar, S.H.; Paul, H.D.; Daniel, P.B.; Catie, S.B.; Dinkorma, O.; David, S.R. Intergrative Genomic Approaches Highlight a Family of Parasite-Specific Kinases that Regulate Host Responses. Cell Host Microbe 2010, 8, 208–218. [Google Scholar] [CrossRef]
  21. Guo, L.; Zhao, X.; Zhang, J. Advances in the study of rhoptry proteins of Toxoplasma gondii and nucleic acid vaccines against toxoplasmosis. J. Pathog. Biol. 2015, 10, 1–4. [Google Scholar]
  22. Stuart, W.; Juliane, S.; Juliane, S.; Robin, P. MAP Kinase Phosphatase-2 Plays a Key Role in the Control of Infection with Toxoplasma gondii by Modulating iNOS and Arginase-1 Activities in Mice. PLoS Pathog. 2013, 9, 1–14. [Google Scholar] [CrossRef]
  23. Xu, P.; Cao, L.; Li, X.; Zeng, D.W.; Quan, Z.; Quan, L. Bioinformatic analysis of the structure and function of MAPK protein encoded by Toxoplasma gondii. Heilongjiang Anim. Sci. Vet. Med. 2015, 17, 1–4, 291. [Google Scholar]
  24. Sun, X. Proliferation of Toxoplasma gondii tachyzoites and its expression of mitogen activated protein kinases in host cells. J. Bengbu Med. Coll. 2004, 4, 283–284, 294. [Google Scholar]
  25. Sun, X. The blocking effect of mitogen activated protein kinases inhibitor to the cellular signaling pathway on Toxoplasma gondii tachyzoites invading to host cells. J. Trop. Dis. Parasitol. 2004, 2, 14–15, 28, 66. [Google Scholar]
  26. Yang, X.; Chen, X.; Sun, X.; Xia, H.; Fang, Q.; Hu, S.; Xu, S.; Wang, Y. The influence of mitogen activated protein kinases inhibitor on the Toxoplasma gondii tachyzoites invading to host cells. J. Trop. Dis. Parasitol. 2006, 4, 5–7, 30. [Google Scholar]
  27. Yang, X.; Chen, X.; Xu, J.; Sun, X.; Chang, X.; Wang, Y.; Hu, S.; Ge, X.; Li, B. Two mitogen activated protein kinases inhibitors on the Toxoplasma gondii tachyzoites invading to host cells. Chin. J. Zoonoses 2009, 25, 97–99. [Google Scholar]
  28. Wang, H. Cloning, Expression and Characterization of MAPK Genes from Echinococcus granulosus. Master’s Thesis, Xinjiang University, Urumchi, China, May 2010. [Google Scholar]
  29. Lv, H. The role of mitogen-activated protein kinase on the proliferation and apoptosis of Echinococcus granulosus. Ph.D. Thesis, Huazhong University of Science and Technology, Wuhan, China, October 2014. [Google Scholar]
  30. Zhe, C.; Fan, L.; Xiu, L.; Mengya, D.; Jianjian, W.; Xinrui, G.; Huimin, T.; Zhijie, H.; Ying, L.; Xiaoli, C.; et al. EGF-mediated EGFR/ERK signaling pathway promotes germinative cell proliferation in Echinococcus multilocularis that contributes to larval growth and development. PLoS Negl. Trop. Dis. 2017, 11, 1–18. [Google Scholar] [CrossRef]
Figure 1. Simplified MAPK signaling pathways. (A) ERK1/2 pathway. (B) p38 α, β, δ, and γ pathways. (C) JNK 1, 2, and 3 pathways [6].
Figure 1. Simplified MAPK signaling pathways. (A) ERK1/2 pathway. (B) p38 α, β, δ, and γ pathways. (C) JNK 1, 2, and 3 pathways [6].
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Table 1. MAPK pathways in host cell infected by parasite.
Table 1. MAPK pathways in host cell infected by parasite.
Host Cell Infected by ParasitePathological ImportanceThe Role of the PathwayReference
Mice liver cells infected by E. multilocularisHepatocyte apoptosis after proliferation as well as damage of liver structure and function.Early infection: Activation of ERK1/2 contribute to hypatocyte proliferation.
Terminal infection: Activation of JNK contribute to hypatocyte apoptosis.
[9]
Mouse macrophage cell line (RAW264.7) cultured and treated with CsLysoPLAHepatic fibrosis during C. sinensis infection as well as damage of liver structure and function.PKA-dependent B-Raf/ERK1/2 pathway in mouse macrophages was activated by CsLysoPLA→upregulated production of IL-25→activates HSCs.[12]
BeWo trophoblastic cell line infected by T. cruziCause trophoblast epithelium turnover, which is considered as part of innate immunity.Participate Bevo trophoblast maintenance and differentiation.[7]
Neutrophil infected by L. amazonensisNeutrophils netosis can kill parasite.L. amazonensis induce neutrophils netosis through ERK pathway, which acti-vation downstream of PI3Kg and upstream of ROS generation.[15]
Macrophages infected by Leishmania spp. and T. cruziHighjack the immune response, and, in this manner, promote parasite maintenance in the host.Parasite target on macrophages MAPK pathways to modulate host immune system and to favor it replication and survival.[16]
Human THP-1 Cells infected by T. gondiiIL-23 and IL-12 regulate both innate and adaptive immunity.IL-23 production in T. gondii-infected THP-1 cells was regulated by ERK1/2.
IL-12 production in T. gondii-infected THP-1 cells was regulated by p38 MAPK and JNK.
[17]
Table 2. MAPK pathways in parasite cell.
Table 2. MAPK pathways in parasite cell.
ParasiteThe Role of the PathwayReference
T. gondiiPlay an important role in tachyzoite invasion and proliferation.[10]
E. multilocularisPromote growth of metacestodes and germinative cell proliferation.[30]
L. donovaniLeads to apoptotic cell death in parasite.[11]

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