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Review Article

The limited knowledge of placental damage due to neglected infections: ongoing problems in Latin America

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Pages 151-169 | Received 03 Nov 2019, Accepted 08 Mar 2020, Published online: 02 Jun 2020
 

ABSTRACT

The placenta works as a selective barrier, protecting the fetus from potential infections that may affect the maternal organism during pregnancy. In this review, we will discuss several challenging infections that are common within Latin American countries and that may affect the maternal-fetal interface and pose risks to fetal development. Specifically, we will focus on emerging infectious diseases including the arboviruses, malaria, leishmaniasis, and the bacterial foodborne disease caused by Shiga toxin-producing Escherichia coli. We will also highlight some topics of interest currently being studied by research groups that comprise an international effort aimed at filling the knowledge gaps in this field. These topics address the relationship between exposure to microorganisms and placental abnormalities, congenital anomalies, and complications of pregnancy.

Abbreviations

ADE: antibody-dependent enhancement; CCL2: monocyte chemoattractant protein-1; CCL3: macrophage inflammatory protein-1 α; CCL5: chemokine (C-C motif) ligand 5; CHIKV: chikungunya virus; DCL: diffuse cutaneous leishmaniasis; DENV: dengue virus; Gb3: glycolipid globotriaosylceramyde; HIF: hypoxia-inducible factor; HUS: hemolytic uremic syndrome; IFN: interferon; Ig: immunoglobulins; IL: interleukin; IUGR: intrauterine growth restriction; LCL: localized cutaneous leishmaniasis; LPS: lipopolysaccharid; MCL: mucocutaneous leishmaniasis; NO: nitric oxide; PCR: polymerase chain reaction; PGF: placental growth factor; PM: placental malaria; RIVATREM: Red Iberoamericana de Alteraciones Vasculares em transtornos del Embarazo; sVEGFR: soluble vascular endothelial growth factor receptor; STEC: shiga toxin-producing Escherichia coli; stx: shiga toxin protein; TNF: tumor necrosis factor; TOAS: T cell original antigenic sin; Var2CSA: variant surface antigen 2-CSA; VEGF: vascular endothelial growth factor; VL: visceral leishmaniasis; WHO: world health organization; YFV: yellow fever virus; ZIKV: Zika virus

Disclosure statement

The authors declare no conflict of interest.

Authors contributions

Manuscript writing (Leishmania): IMR, PCSS; manuscript writing (Arboviruses infection): AUB, ELLT; manuscript writing (Placental Dysbiosis and Microbiota): AC, AMA; manuscript writing (Malaria): JB, OA; manuscript writing (Introduction and Conclusion remarks): RGR, PA-R; manuscript writing (Shiga toxin-producing Escherichia coli): FS, AED, CI; project development, conceptualization, writing – review & editing: CE, TS, FRG; manuscript writing (Leishmania) and project administration: VVL.

Additional information

Funding

Colciencias Colombia (#111580762949-2019 to A.P.C.; #520165740853 2014-2019 to J.C.B. and Ph.D. fellowship/2010 to A.M.A.); PPSUS/Decit/MS/CNPq/SESAU-AL/FAPEAL 06/2016:60030 000819/2016 to A.U.B.); Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Conselho Nacional de Desenvolvimento Científico e Tecnológico (PPSUS/Decit/MS/CNPq/SESAU-AL/FAPEMAT 032.4552/2018 and CNPq 306166/2019-4 to F.R.G.), University of Antioquia (2019; Medellín, Colombia to J.C.B.). CE is financially supported by DIUBB 184309 4/R, GI 171709/VC, REDI170287, and REDI170373

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