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Recent insights into innate and adaptive immune responses to Giardia

·2019·Advances in Parasitology

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  1. Abreu, 2010, Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function, Nat. Rev. Immunol., 10, 131, 10.1038/nri2707 · DOI · Paper page
  2. Adam, 2001, Biology of Giardia lamblia, Clin. Microbiol. Rev., 14, 447, 10.1128/CMR.14.3.447-475.2001 · DOI
  3. Aley, 1994, Killing of Giardia lamblia by cryptdins and cationic neutrophil peptides, Infect. Immun., 62, 5397, 10.1128/iai.62.12.5397-5403.1994 · DOI
  4. Allain, 2018, Bile salt hydrolase activities: a novel target to screen anti-Giardia lactobacilli?, Front. Microbiol., 9, 89, 10.3389/fmicb.2018.00089 · DOI
  5. Amat, 2017, Cysteine protease-dependent mucous disruptions and differential mucin gene expression in Giardia duodenalis infection, Am. J. Pathol., 187, 2486, 10.1016/j.ajpath.2017.07.009 · DOI
  6. Andersen, 2006, Adaptive immunity-dependent intestinal hypermotility contributes to host defense against Giardia spp, Infect. Immun., 74, 2473, 10.1128/IAI.74.4.2473-2476.2006 · DOI
  7. Babaei, 2016, Adaptive immune response in symptomatic and asymptomatic enteric protozoal infection: evidence for a determining role of parasite genetic heterogeneity in host immunity to human giardiasis, Microbes Infect., 18, 687, 10.1016/j.micinf.2016.06.009 · DOI
  8. Barash, 2017, Giardia alters commensal microbial diversity throughout the murine gut, Infect. Immun., 85, 10.1128/IAI.00948-16 · DOI
  9. Bartelt, 2013, Persistent G. lamblia impairs growth in a murine malnutrition model, J. Clin. Invest., 123, 2672, 10.1172/JCI67294 · DOI
  10. Bartelt, 2017, Cross-modulation of pathogen-specific pathways enhances malnutrition during enteric co-infection with Giardia lamblia and enteroaggregative Escherichia coli, PLoS Pathog., 13, 10.1371/journal.ppat.1006471 · DOI
  11. Beatty, 2017, Giardia duodenalis induces pathogenic dysbiosis of human intestinal microbiota biofilms, Int. J. Parasitol., 47, 311, 10.1016/j.ijpara.2016.11.010 · DOI · Paper page
  12. Benyacoub, 2005, Enterococcus faecium SF68 enhances the immune response to Giardia intestinalis in mice, J. Nutr., 135, 1171, 10.1093/jn/135.5.1171 · DOI
  13. Bhargava, 2015, Giardia duodenalis surface cysteine proteases induce cleavage of the intestinal epithelial cytoskeletal protein villin via myosin light chain kinase, PLoS One, 10, 10.1371/journal.pone.0136102 · DOI
  14. Bienz, 2003, Interleukin-6-deficient mice are highly susceptible to Giardia lamblia infection but exhibit normal intestinal immunoglobulin a responses against the parasite, Infect. Immun., 71, 1569, 10.1128/IAI.71.3.1569-1573.2003 · DOI
  15. Byrd, 1994, Giardia lamblia infections in adult mice, Infect. Immun., 62, 3583, 10.1128/iai.62.8.3583-3585.1994 · DOI
  16. Cabrera-Licona, 2017, Expression and secretion of the Giardia duodenalis variant surface protein 9B10A by transfected trophozoites causes damage to epithelial cell monolayers mediated by protease activity, Exp. Parasitol., 179, 49, 10.1016/j.exppara.2017.06.006 · DOI
  17. Cao, 2012, Th17 cells upregulate polymeric Ig receptor and intestinal IgA and contribute to intestinal homeostasis, J. Immunol., 189, 4666, 10.4049/jimmunol.1200955 · DOI
  18. Chen, 2013, Persistent gut barrier damage and commensal bacterial influx following eradication of Giardia infection in mice, Gut Pathog., 5, 26, 10.1186/1757-4749-5-26 · DOI
  19. Chin, 2002, Strain-dependent induction of enterocyte apoptosis by Giardia lamblia disrupts epithelial barrier function in a caspase-3-dependent manner, Infect. Immun., 70, 3673, 10.1128/IAI.70.7.3673-3680.2002 · DOI
  20. Cotton, 2014, Giardia duodenalis cathepsin B proteases degrade intestinal epithelial interleukin-8 and attenuate interleukin-8-induced neutrophil chemotaxis, Infect. Immun., 82, 2772, 10.1128/IAI.01771-14 · DOI
  21. Cotton, 2014, Giardia duodenalis infection reduces granulocyte infiltration in an in vivo model of bacterial toxin-induced colitis and attenuates inflammation in human intestinal tissue, PLoS One, 9, 10.1371/journal.pone.0109087 · DOI
  22. Dann, 2015, IL-17A promotes protective IgA responses and expression of other potential effectors against the lumen-dwelling enteric parasite Giardia, Exp. Parasitol., 156, 68, 10.1016/j.exppara.2015.06.003 · DOI
  23. Dann, 2018, Infection of the small intestine induces chronic colitis in genetically susceptible hosts, J. Immunol., 201, 548, 10.4049/jimmunol.1700824 · DOI
  24. Davids, 2006, Polymeric immunoglobulin receptor in intestinal immune defense against the lumen-dwelling protozoan parasite Giardia, J. Immunol., 177, 6281, 10.4049/jimmunol.177.9.6281 · DOI
  25. de Carvalho, 2008, Protease activity in extracellular products secreted in vitro by trophozoites of Giardia duodenalis, Parasitol. Res., 104, 185, 10.1007/s00436-008-1185-z · DOI
  26. Dreesen, 2012, Microarray analysis of the intestinal host response in Giardia duodenalis assemblage E infected calves, PLoS One, 7, 10.1371/journal.pone.0040985 · DOI
  27. Dreesen, 2014, Giardia muris infection in mice is associated with a protective interleukin 17A response and induction of peroxisome proliferator-activated receptor alpha, Infect. Immun., 82, 3333, 10.1128/IAI.01536-14 · DOI
  28. Dubourg, 2018, Giardia secretome highlights secreted tenascins as a key component of pathogenesis, Gigascience, 7, 1, 10.1093/gigascience/giy003 · DOI
  29. Eckmann, 2000, Nitric oxide production by human intestinal epithelial cells and competition for arginine as potential determinants of host defense against the lumen-dwelling pathogen Giardia lamblia, J. Immunol., 164, 1478, 10.4049/jimmunol.164.3.1478 · DOI
  30. El-Gebaly, 2012, Saliva and sera IgA and IgG in Egyptian Giardia-infected children, Parasitol. Res., 111, 571, 10.1007/s00436-012-2869-y · DOI
  31. Evans-Osses, 2010, Involvement of lectin pathway activation in the complement killing of Giardia intestinalis, Biochem. Biophys. Res. Commun., 395, 382, 10.1016/j.bbrc.2010.04.025 · DOI
  32. Feng, 2016, Vaccination with bivalent DNA vaccine of α1-Giardin and CWP2 delivered by attenuated Salmonella typhimurium reduces Trophozoites and cysts in the feces of mice infected with Giardia lamblia, PLoS One, 11
  33. Fink, 2017, The intersection of immune responses, microbiota, and pathogenesis in giardiasis, Trends Parasitol., 33, 901, 10.1016/j.pt.2017.08.001 · DOI
  34. Fisher, 2013, Modeling long-term host cell-Giardia lamblia interactions in an in vitro co-culture system, PLoS One, 8, 10.1371/journal.pone.0081104 · DOI
  35. Frontera, 2018, Lactoferrin and lactoferricin endocytosis halt Giardia cell growth and prevent infective cyst production, Sci. Rep., 8, 18020, 10.1038/s41598-018-36563-1 · DOI
  36. Gerbaba, 2015, Giardia duodenalis-induced alterations of commensal bacteria kill Caenorhabditis elegans: a new model to study microbial-microbial interactions in the gut, Am. J. Physiol. Gastrointest. Liver Physiol., 308, G550, 10.1152/ajpgi.00335.2014 · DOI
  37. Goyal, 2013, Probiotic lactobacillus rhamnosus GG modulates the mucosal immune response in Giardia intestinalis-infected BALB/c mice, Dig. Dis. Sci., 58, 1218, 10.1007/s10620-012-2503-y · DOI
  38. Goyal, 2013, Lactobacillus rhamnosus GG antagonizes Giardia intestinalis induced oxidative stress and intestinal disaccharidases: an experimental study, World J. Microbiol. Biotechnol., 29, 1049, 10.1007/s11274-013-1268-6 · DOI
  39. Hagel, 2011, Co-infection with Ascaris lumbricoides modulates protective immune responses against Giardia duodenalis in school Venezuelan rural children, Acta Trop., 117, 189, 10.1016/j.actatropica.2010.12.001 · DOI
  40. Hanevik, 2012, Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome, BMC Infect. Dis., 12, 258, 10.1186/1471-2334-12-258 · DOI
  41. Hanevik, 2017, Giardia-specific cellular immune responses in post-giardiasis chronic fatigue syndrome, BMC Immunol., 18, 5, 10.1186/s12865-017-0190-3 · DOI
  42. Hill, 1984, Susceptibility of Giardia lamblia trophozoites to the lethal effect of human serum, J. Immunol., 132, 2046, 10.4049/jimmunol.132.4.2046 · DOI
  43. Hjøllo, 2018, Longitudinal cohort study of serum antibody responses towards Giardia lamblia variant-specific surface proteins in a non-endemic area, Exp. Parasitol., 191, 66, 10.1016/j.exppara.2018.06.005 · DOI
  44. Humen, 2005, Lactobacillus johnsonii La1 antagonizes Giardia intestinalis in vivo, Infect. Immun., 73, 1265, 10.1128/IAI.73.2.1265-1269.2005 · DOI
  45. Jiménez, 2000, Identification and partial characterization of excretory/secretory products with proteolytic activity in Giardia intestinalis, J. Parasitol., 86, 859, 10.1645/0022-3395(2000)086[0859:IAPCOE]2.0.CO;2 · DOI
  46. Jimenez, 2014, Antibody and cytokine responses to Giardia excretory/secretory proteins in Giardia intestinalis-infected BALB/c mice, Parasitol. Res., 113, 2709, 10.1007/s00436-014-3927-4 · DOI
  47. Kamda, 2009, Phosphoinositide 3-kinase-dependent inhibition of dendritic cell interleukin-12 production by Giardia lamblia, Infect. Immun., 77, 685, 10.1128/IAI.00718-08 · DOI
  48. Kamda, 2012, Giardia duodenalis: dendritic cell defects in IL-6 deficient mice contribute to susceptibility to intestinal infection, Exp. Parasitol., 130, 288, 10.1016/j.exppara.2012.01.003 · DOI
  49. Keselman, 2016, The microbiota contributes to CD8+ T cell activation and nutrient malabsorption following intestinal infection with Giardia duodenalis, Infect. Immun., 84, 2853, 10.1128/IAI.00348-16 · DOI
  50. Lee, 2012, Excretory-secretory products of Giardia lamblia induce interleukin-8 production in human colonic cells via activation of p38, ERK1/2, NF-κB and AP-1, Parasite Immunol., 34, 183, 10.1111/j.1365-3024.2012.01354.x · DOI
  51. Lee, 2014, Giardia lamblia binding immunoglobulin protein triggers maturation of dendritic cells via activation of TLR4-MyD88-p38 and ERK1/2 MAPKs, Parasite Immunol., 36, 627, 10.1111/pim.12119 · DOI
  52. Li, 2004, Mast cell-dependent control of Giardia lamblia infections in mice, Infect. Immun., 72, 6642, 10.1128/IAI.72.11.6642-6649.2004 · DOI
  53. Li, 2006, Neuronal nitric oxide synthase is necessary for elimination of Giardia lamblia infections in mice, J. Immunol., 176, 516, 10.4049/jimmunol.176.1.516 · DOI
  54. Li, 2007, Mast cell mediated changes in smooth muscle contractility during mouse giardiasis, Infect. Immun., 75, 4514, 10.1128/IAI.00596-07 · DOI
  55. Li, 2014, Resistance to reinfection in mice as a vaccine model for giardiasis, Hum. Vaccin. Immunother., 10, 1536, 10.4161/hv.29116 · DOI
  56. Li, 2016, Complement activation by Giardia duodenalis parasites through the Lectin pathway contributes to mast cell responses and parasite control, Infect. Immun., 84, 1092, 10.1128/IAI.00074-16 · DOI
  57. Li, 2017, TLR2−/− mice display decreased severity of giardiasis via enhanced proinflammatory cytokines production dependent on AKT signal pathway, Front. Immunol., 8, 1186, 10.3389/fimmu.2017.01186 · DOI
  58. Li, 2018, Mucocutaneous IL-17 immunity in mice and humans: host defense vs. excessive inflammation, Mucosal Immunol., 11, 581, 10.1038/mi.2017.97 · DOI
  59. Li, 2018, Mouse macrophages capture and kill Giardia lamblia by means of releasing extracellular trap, Dev. Comp. Immunol., 88, 206, 10.1016/j.dci.2018.07.024 · DOI
  60. Liu, 2018, Secreted Giardia intestinalis cysteine proteases disrupt intestinal epithelial cell junctional complexes and degrade chemokines, Virulence, 9, 879, 10.1080/21505594.2018.1451284 · DOI
  61. Liu, 2019, Cleavage specificity of recombinant Giardia intestinalis cysteine proteases: degradation of immunoglobulins and defensins, Mol. Biochem. Parasitol., 227, 29, 10.1016/j.molbiopara.2018.10.004 · DOI
  62. Lopez-Romero, 2017, Characterization of BIP protein of G. lamblia as a potential immunogen in a mouse infection model, Immunobiology, 222, 884, 10.1016/j.imbio.2017.05.008 · DOI
  63. Ma'ayeh, 2017, Characterization of the Giardia intestinalis secretome during interaction with human intestinal epithelial cells: the impact on host cells, PLoS Negl. Trop. Dis., 11
  64. Ma'ayeh, 2018, Responses of the differentiated intestinal epithelial cell line Caco-2 to infection with the, Front. Cell. Infect. Microbiol., 8, 244, 10.3389/fcimb.2018.00244 · DOI
  65. Maloney, 2015, Macrophages expressing arginase 1 and nitric oxide synthase 2 accumulate in the small intestine during Giardia lamblia infection, Microbes Infect., 17, 462, 10.1016/j.micinf.2015.03.006 · DOI
  66. Manko, 2017, Giardia co-infection promotes the secretion of antimicrobial peptides beta-defensin 2 and trefoil factor 3 and attenuates attaching and effacing bacteria-induced intestinal disease, PLoS One, 12, 10.1371/journal.pone.0178647 · DOI
  67. Nash, 1985, Differences in excretory-secretory products and surface antigens among 19 isolates of Giardia, J. Infect. Dis., 152, 1166, 10.1093/infdis/152.6.1166 · DOI
  68. Nash, 1983, Excretory-secretory products of Giardia lamblia, J. Immunol., 131, 2004, 10.4049/jimmunol.131.4.2004 · DOI
  69. Obendorf, 2013, Increased expression of CD25, CD83, and CD86, and secretion of IL-12, IL-23, and IL-10 by human dendritic cells incubated in the presence of toll-like receptor 2 ligands and Giardia duodenalis, Parasit. Vectors, 6, 317, 10.1186/1756-3305-6-317 · DOI
  70. Ortega-Pierres, 2018, Giardipain-1, a protease secreted by Giardia duodenalis trophozoites, causes junctional, barrier and apoptotic damage in epithelial cell monolayers, Int. J. Parasitol., 48, 621, 10.1016/j.ijpara.2018.01.006 · DOI
  71. Paerewijck, 2017, Interleukin-17 receptor A (IL-17RA) as a central regulator of the protective immune response against Giardia, Sci. Rep., 7, 8520, 10.1038/s41598-017-08590-x · DOI
  72. Perez, 2001, Inhibition of Giardia intestinalis by extracellular factors from lactobacilli: an in vitro study, Appl. Environ. Microbiol., 67, 5037, 10.1128/AEM.67.11.5037-5042.2001 · DOI
  73. Prucca, 2008, Antigenic variation in Giardia lamblia is regulated by RNA interference, Nature, 456, 750, 10.1038/nature07585 · DOI
  74. Prucca, 2011, Regulation of antigenic variation in Giardia lamblia, Annu. Rev. Microbiol., 65, 611, 10.1146/annurev-micro-090110-102940 · DOI
  75. Quintero, 2013, Identification of an immunogenic protein of Giardia lamblia using monoclonal antibodies generated from infected mice, Mem. Inst. Oswaldo Cruz, 108, 616, 10.1590/0074-0276108052013013 · DOI
  76. Quintero, 2017, Isolation and partial characterization of an immunogenic antigen of Giardia lamblia, Parasitol. Int., 66, 324, 10.1016/j.parint.2017.01.007 · DOI · Paper page
  77. Ratner, 2008, Changes in the N-glycome, glycoproteins with Asn-linked glycans, of Giardia lamblia with differentiation from trophozoites to cysts, Eukaryot. Cell, 7, 1930, 10.1128/EC.00268-08 · DOI
  78. Rivero, 2010, Disruption of antigenic variation is crucial for effective parasite vaccine, Nat. Med., 16, 551, 10.1038/nm.2141 · DOI
  79. Rodriguez-Fuentes, 2006, Giardia duodenalis: analysis of secreted proteases upon trophozoite-epithelial cell interaction in vitro, Mem. Inst. Oswaldo Cruz, 101, 693, 10.1590/S0074-02762006000600020 · DOI
  80. Rogawski, 2017, Determinants and impact of Giardia infection in the first 2 years of life in the MAL-ED birth cohort, J. Pediatric. Infect. Dis. Soc., 6, 153, 10.1093/jpids/piw082 · DOI
  81. Rogawski, 2018, Use of quantitative molecular diagnostic methods to investigate the effect of enteropathogen infections on linear growth in children in low-resource settings: longitudinal analysis of results from the MAL-ED cohort study, Lancet Glob. Health, 6, e1319, 10.1016/S2214-109X(18)30351-6 · DOI · Paper page
  82. Roxstrom-Lindquist, 2005, Giardia lamblia-induced changes in gene expression in differentiated Caco-2 human intestinal epithelial cells, Infect. Immun., 73, 8204, 10.1128/IAI.73.12.8204-8208.2005 · DOI
  83. Saghaug, 2016, Human memory CD4+ T cell immune responses against Giardia lamblia, Clin. Vaccine Immunol., 23, 11, 10.1128/CVI.00419-15 · DOI
  84. Samra, 1988, Effect of excretory-secretory products of Giardia lamblia on glucose and phenylalanine transport in the small intestine of Swiss albino mice, Biochem. Int., 17, 801
  85. Scott, 2002, Intestinal infection with Giardia spp. reduces epithelial barrier function in a myosin light chain kinase-dependent fashion, Gastroenterology, 123, 1179, 10.1053/gast.2002.36002 · DOI
  86. Scott, 2004, Role of CD8+ and CD4+ T lymphocytes in jejunal mucosal injury during murine giardiasis, Infect. Immun., 72, 3536, 10.1128/IAI.72.6.3536-3542.2004 · DOI
  87. Serradell, 2016, Vaccination of domestic animals with a novel oral vaccine prevents, NPJ Vaccines, 1, 16018, 10.1038/npjvaccines.2016.18 · DOI
  88. Serradell, 2018, Cytokines, antibodies, and histopathological profiles during Giardia infection and variant-specific surface protein-based vaccination, Infect. Immun., 86, 10.1128/IAI.00773-17 · DOI
  89. Serradell, 2019, Efficient oral vaccination by bioengineering virus-like particles with protozoan surface proteins, Nat. Commun., 10, 361, 10.1038/s41467-018-08265-9 · DOI
  90. Shukla, 2008, Effect of Lactobacillus casei as a probiotic on modulation of giardiasis, Dig. Dis. Sci., 53, 2671, 10.1007/s10620-007-0197-3 · DOI
  91. Shukla, 2013, Oral Administration of the Probiotic Lactobacillus casei ameliorates gut morphology and physiology in malnourished-Giardia intestinalis-infected BALB/c mice, ISRN Parasitol., 2013, 762638, 10.5402/2013/762638 · DOI
  92. Shukla, 2019, Comparative analysis of Antigiardial potential of heat inactivated and probiotic protein of probiotic lactobacillus rhamnosus GG in murine giardiasis, Probiotics Antimicrob. Proteins
  93. Singer, 2000, The role of Normal Flora in Giardia lamblia infections in mice, J. Infect. Dis., 181, 1510, 10.1086/315409 · DOI
  94. Singer, 2000, T-cell-dependent control of acute Giardia lamblia infections in mice, Infect. Immun., 68, 170, 10.1128/IAI.68.1.170-175.2000 · DOI
  95. Solaymani-Mohammadi, 2010, Giardia duodenalis: the double-edged sword of immune responses in giardiasis, Exp. Parasitol., 126, 292, 10.1016/j.exppara.2010.06.014 · DOI
  96. Solaymani-Mohammadi, 2011, Host immunity and pathogen strain contribute to intestinal disaccharidase impairment following gut infection, J. Immunol., 187, 3769, 10.4049/jimmunol.1100606 · DOI
  97. Stadelmann, 2012, Arginine consumption by the intestinal parasite Giardia intestinalis reduces proliferation of intestinal epithelial cells, PLoS One, 7, 10.1371/journal.pone.0045325 · DOI
  98. Summan, 2018, Modulation of human dendritic cell activity by Giardia and helminth antigens, Parasite Immunol., 40, 10.1111/pim.12525 · DOI
  99. Tako, 2013, Transcriptomic analysis of the host response to Giardia duodenalis infection reveals redundant mechanisms for parasite control, MBio, 4, 10.1128/mBio.00660-13 · DOI
  100. Toro-Londono, 2019, Intestinal parasitic infection alters bacterial gut microbiota in children, PeerJ, 7, 10.7717/peerj.6200 · DOI
  101. Torres, 2000, Influence of bacteria from the duodenal microbiota of patients with symptomatic giardiasis on the pathogenicity of Giardia duodenalis in gnotoxenic mice, J. Med. Microbiol., 49, 209, 10.1099/0022-1317-49-3-209 · DOI
  102. Travers, 2016, Deconjugated bile salts produced by extracellular bile-salt hydrolase-like activities from the probiotic lactobacillus johnsonii La1 inhibit Giardia duodenalis in vitro growth, Front. Microbiol., 7, 1453, 10.3389/fmicb.2016.01453 · DOI
  103. Troeger, 2007, Effect of chronic Giardia lamblia infection on epithelial transport and barrier function in human duodenum, Gut, 56, 328, 10.1136/gut.2006.100198 · DOI · Paper page
  104. Ward, 1988, Biology of Giardia lamblia. Detection of N-acetyl-D-glucosamine as the only surface saccharide moiety and identification of two distinct subsets of trophozoites by lectin binding, J. Exp. Med., 167, 73, 10.1084/jem.167.1.73 · DOI
  105. Weatherhead, 2017, Comparison of cytokine responses in Ecuadorian children infected with, Am. J. Trop. Med. Hyg., 96, 1394, 10.4269/ajtmh.16-0580 · DOI
  106. Zarebavani, 2012, Serum levels of zinc, copper, vitamin B12, folate and immunoglobulins in individuals with giardiasis, Iran. J. Public Health, 41, 47
  107. Zhou, 2003, Role of interleukin-6 in the control of acute and chronic Giardia lamblia infections in mice, Infect. Immun., 71, 1566, 10.1128/IAI.71.3.1566-1568.2003 · DOI
  108. Zhou, 2007, Tumour necrosis factor alpha contributes to protection against Giardia lamblia infection in mice, Parasite Immunol., 29, 367, 10.1111/j.1365-3024.2007.00953.x · DOI

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Venue
Advances in Parasitology
Publisher
Elsevier
Published
2019
Pages
171-208
ISSN
0065-308X
Cited by
50
References
2
Language
en
Funders
National Institutes of Health

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Recent insights into innate and adaptive immune responses to Giardia. (2019). Advances in Parasitology. https://doi.org/10.1016/bs.apar.2019.07.004