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Letter to the Editor

Persistent Zika virus infection in porcine conceptuses is associated with elevated in utero cortisol levels

ORCID Icon, , , , , & show all
Pages 1338-1343 | Received 04 Apr 2018, Accepted 23 Jul 2018, Published online: 26 Aug 2018

References

  • Wood CE, Keller-Wood M. The critical importance of the fetal hypothalamus-pituitary-adrenal axis. F1000Research. 2016;5:F1000 Faculty Rev-115.
  • French NP, Hagan R, Evans SF, et al. Repeated antenatal corticosteroids: size at birth and subsequent development. Am J Obstet Gynecol. 1999;180:114–121.
  • Enwonwu CO, Meeks VI, Sawiris PG. Elevated cortisol levels in whole saliva in HIV infected individuals. Eur J Oral Sci. 1996;104:322–324.
  • Trevisan M, Matkovic U, Cusinato R, et al. Human cytomegalovirus productively infects adrenocortical cells and induces an early cortisol response. J Cell Physiol. 2009;221:629–641.
  • Fan X, Wang K, Fan Y. [Study of serum level of cortisol and peripheral T lymphocyte subsets state in the hepatitis B virus carriers]. Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2008;22:330–332.
  • Rasmussen SA, Jamieson DJ, Honein MA, et al. Zika virus and birth defects? Reviewing the evidence for causality. N Engl J Med. 2016;374:1981–1987.
  • Reynolds RM. Glucocorticoid excess and the developmental origins of disease: two decades of testing the hypothesis - 2012 curt richter award winner. Psychoneuroendocrinology. 2013;38:1–11.
  • Tabata T, Petitt M, Puerta-Guardo H, et al. Zika Virus replicates in proliferating cells in explants from first-trimester human placentas, potential sites for dissemination of infection. J Infect Dis. 2017;217(8):1202–1213.
  • Corry J, Arora N, Good CA, et al. Organotypic models of type III interferon-mediated protection from Zika virus infections at the maternal–fetal interface. Proc Natl Acad Sci. 2017;114:9433–9438.
  • Bhatnagar J, Rabeneck DB, Martines RB, et al. Zika virus RNA replication and persistence in brain and placental tissue. Emerg Infect Dis. 2017;23:405-414.
  • Kossintseva I, Wong S, Johnstone E, et al. Proinflammatory cytokines inhibit human placental 11beta-hydroxysteroid dehydrogenase type 2 activity through Ca2+ and cAMP pathways. Am J Physiol Endocrinol Metab. 2006;290:E282–8.
  • Kanitz E, Otten W, Tuchscherer M. Changes in endocrine and neurochemical profiles in neonatal pigs prenatally exposed to increased maternal cortisol. J Endocrinol. 2006;191:207–220.
  • Darbellay J, Cox B, Lai K, et al. Zika virus causes persistent infection in porcine conceptuses and may impair health in offspring. EBioMedicine. 2017;25:73–86.
  • Lind NM, Moustgaard A, Jelsing J, et al. The use of pigs in neuroscience: modeling brain disorders. Neurosci Biobehav Rev. 2007;31:728–751.
  • Otten W, Kanitz E, Couret D, et al. Maternal social stress during late pregnancy affects hypothalamic-pituitary-adrenal function and brain neurotransmitter systems in pig offspring. Domest Anim Endocrinol. 2010;38:146–156.
  • Daniel JA, Keisler DH, Sterle JA, et al. Birth by caesarian section alters postnatal function of the hypothalamic-pituitary-adrenal axis in young pigs. J Anim Sci. 1999;77:742–749.
  • Haussmann MF, Carroll JA, Weesner GD, et al. Administration of ACTH to restrained, pregnant sows alters their pigs’ hypothalamic-pituitary-adrenal (HPA) axis. J Anim Sci. 2000;78:2399–2411.
  • Klemcke HG, Christenson RK. Porcine placental 11 beta-hydroxysteroid dehydrogenase activity. Biol Reprod. 1996;55:217–223.
  • Klemcke HG. Dehydrogenase and oxoreductase activities of porcine placental 11beta-hydroxysteroid dehydrogenase. Life Sci. 2000;66:1045–1052.
  • Klemcke HG, Sampath Kumar R, Yang K, et al. 11β-hydroxysteroid dehydrogenase and glucocorticoid receptor messenger RNA expression in porcine placentae: effects of stage of gestation, breed, and uterine environment. Biol Reprod. 2003;69:1945–1950.
  • Darbellay J, Lai K, Babiuk S, et al. Neonatal pigs are susceptible to experimental Zika virus infection. Emerg Microbes Infect. 2017;6:e6.
  • Zupan M, Zanella AJ. Peripheral regulation of stress and fear responses in pigs from tail-biting pens. Rev Bras Zootec. 2017;46:33–38.
  • Turpin D, Langendijk P, Chen T-Y, et al. Intermittent suckling causes a transient increase in cortisol that does not appear to compromise selected measures of piglet welfare and stress. Animals. 2016;6:24.
  • Turpin D, Langendijk P, Chen T-Y, et al. Intermittent suckling in combination with an older weaning age improves growth, feed intake and aspects of gastrointestinal tract carbohydrate absorption in pigs after weaning. Animals. 2016;6:66.
  • Rault J-L, Dunshea F, Pluske J. Effects of oxytocin administration on the response of piglets to weaning. Animals. 2015;5:545–560.
  • Alonso-Spilsbury M, Mota-Rojas D, Villanueva-García D, et al. Perinatal asphyxia pathophysiology in pig and human: a review. Anim Reprod Sci. 2005;90:1–30.
  • Fujikura T, Klionsky B. The significance of meconium staining. Am J Obstet Gynecol. 1975;121:45–50.
  • Miller NM, Fisk NM, Modi N, et al. Stress responses at birth: determinants of cord arterial cortisol and links with cortisol response in infancy. BJOG. 2005;112:921–926.
  • França GV, Schuler-Faccini L, Oliveira WK, et al. Congenital Zika virus syndrome in Brazil: a case series of the first 1501 livebirths with complete investigation. Lancet. 2016;388:891–897.
  • Sarkar P, Bergman K, O’Connor TG, et al. Maternal antenatal anxiety and amniotic fluid cortisol and testosterone: possible implications for foetal programming. J Neuroendocrinol. 2008;20:489–496.
  • deFencl M, Tulchinsky D. Total cortisol in amniotic fluid and fetal lung maturation. N Engl J Med. 1975;292:133–136.
  • Moura Da Silva AA, Ganz JSS, Sousa PD, et al. Early growth and neurologic outcomes of infants with probable congenital Zika virus syndrome. Emerg Infect Dis. 2016;22:1953–1956.
  • Schreur PJW, Keulen LV, Anjema D, et al. Microencephaly in fetal piglets following in utero inoculation of Zika virus. Emerg Microbes Infect. 2018;7:42.