Prevotella bivia as a source of lipopolysaccharide in the vagina

Anaerobe

Volumn 14, Issue 5, 2008, Pages 256-260

  Aroutcheva, Alla ^a   Ling, Zaodung ^b   Faro, Sebastian ^c  

^a Jr Hospital of Cook County   (United States)

^b RUSH UNIVERSITY   (United States)

^c Women's Hospital of Texas   (United States)

Author keywords

Bacterial vaginosis; Dopamine neurons; E. coli lipopolysaccharides; Gardnerella vaginalis; Prevotella bivia; Rat model

Indexed keywords

CELL EXTRACT; HYDROLASE; LIPOPOLYSACCHARIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BACTERIAL COLONIZATION; CELL COUNT; CELL LYSATE; CLINICAL ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; DOPAMINERGIC NERVE CELL; EMBRYO; ESCHERICHIA COLI; FEMALE; GARDNERELLA VAGINALIS; HUMAN; IMMUNOHISTOCHEMISTRY; NONHUMAN; POLYMERASE CHAIN REACTION; PREVOTELLA BIVIA; PRIORITY JOURNAL; RAT; VAGINA FLORA; VAGINITIS;

ANIMALS; BACTERIAL TOXINS; CELLS, CULTURED; COLONY COUNT, MICROBIAL; ESCHERICHIA COLI; FEMALE; GARDNERELLA VAGINALIS; HUMANS; LIMULUS TEST; LIPOPOLYSACCHARIDES; NEURONS; POLYMERASE CHAIN REACTION; PREVOTELLA; RATS; VAGINA; VAGINOSIS, BACTERIAL;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI; GARDNERELLA VAGINALIS; LIMULUS; PREVOTELLA BIVIA; RATTUS;

EID: 56949084846     PISSN: 10759964     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anaerobe.2008.08.002     Document Type: Article

References (51)

1. Strombeck L., Sandros J., Holst E., et al. Prevotella bivia can invade human cervix epithelial (HeLa) cells. Apmis 115 (2007) 241-251
2. Smayevsky J., Canigia L.F., Lanza A., and Bianchini H. Vaginal microflora associated with bacterial vaginosis in nonpregnant women: reliability of sialidase detection. Infect Dis Obstet Gynecol 9 (2001) 17-22
3. Delaney M.L., and Onderdonk A.B. Nugent score related to vaginal culture in pregnant women. Obstet Gynecol 98 (2001) 79-84
4. Krohn M.A., Hillier S.L., Lee M.L., Rabe L.K., and Eschenbach D.A. Vaginal Bacteroides species are associated with an increased rate of preterm delivery among women in preterm labor. J Infect Dis 164 (1991) 88-93
5. Gibbs R.S., McDuffie Jr. R.S., Kunze M., et al. Experimental intrauterine infection with Prevotella bivia in New Zealand White rabbits. Am J Obstet Gynecol 190 (2004) 1082-1086
6. Dammann O., and Leviton A. Infection remote from the brain, neonatal white matter damage, and cerebral palsy in the preterm infant. Semin Pediatr Neurol 5 (1998) 190-201
7. Edwards A.D., and Tan S. Perinatal infections, prematurity and brain injury. Curr Opin Pediatr 18 (2006) 119-124
8. Endo Y., Shibazaki M., Nakamura M., and Takada H. Contrasting effects of lipopolysaccharides (endotoxins) from oral black-pigmented bacteria and Enterobacteriaceae on platelets, a major source of serotonin, and on histamine-forming enzyme in mice. J Infect Dis 175 (1997) 1404-1412
9. Ling Z., Zhu Y., Tong C., Snyder J.A., Lipton J.W., and Carvey P.M. Progressive dopamine neuron loss following supra-nigral lipopolysaccharide (LPS) infusion into rats exposed to LPS prenatally. Exp Neurol 199 (2006) 499-512
10. Ling Z.D., Chang Q., Lipton J.W., Tong C.W., Landers T.M., and Carvey P.M. Combined toxicity of prenatal bacterial endotoxin exposure and postnatal 6-hydroxydopamine in the adult rat midbrain. Neuroscience 124 (2004) 619-628
11. Amsel R., Totten P.A., Spiegel C.A., Chen K.C., Eschenbach D., and Holmes K.K. Nonspecific vaginitis. Diagnostic criteria and microbial and epidemiologic associations. Am J Med 74 (1983) 14-22
12. Nugent R.P., Krohn M.A., and Hillier S.L. Reliability of diagnosing bacterial vaginosis is improved by a standardized method of gram stain interpretation. J Clin Microbiol 29 (1991) 297-301
13. Zariffard M.R., Saifuddin M., Sha B.E., and Spear G.T. Detection of bacterial vaginosis-related organisms by real-time PCR for Lactobacilli, Gardnerella vaginalis and Mycoplasma hominis. FEMS Immunol Med Microbiol 34 (2002) 277-281
14. Gayle D.A., Ling Z., Tong C., Landers T., Lipton J.W., and Carvey P.M. Lipopolysaccharide (LPS)-induced dopamine cell loss in culture: roles of tumor necrosis factor-alpha, interleukin-1beta, and nitric oxide. Brain Res Dev Brain Res 133 (2002) 27-35
15. Vu T.Q., Ling Z.D., Ma S.Y., et al. Pramipexole attenuates the dopaminergic cell loss induced by intraventricular 6-hydroxydopamine. J Neural Transm 107 (2000) 159-176
16. Nikolaitchouk N., Andersch B., Falsen E., Strombeck L., and Mattsby-Baltzer I. The lower genital tract microbiota in relation to cytokine-, SLPI- and endotoxin levels: application of checkerboard DNA-DNA hybridization (CDH). Apmis 116 (2008) 263-277
17. Aroutcheva A.A., Simoes J.A., Behbakht K., and Faro S. Gardnerella vaginalis isolated from patients with bacterial vaginosis and from patients with healthy vaginal ecosystems. Clin Infect Dis 33 (2001) 1022-1027
18. Pybus V., and Onderdonk A.B. Evidence for a commensal, symbiotic relationship between Gardnerella vaginalis and Prevotella bivia involving ammonia: potential significance for bacterial vaginosis. J Infect Dis 175 (1997) 406-413
19. Thorsen P., Jensen I.P., Jeune B., et al. Few microorganisms associated with bacterial vaginosis may constitute the pathologic core: a population-based microbiologic study among 3596 pregnant women. Am J Obstet Gynecol 178 (1998) 580-587
20. Mikamo H., Kawazoe K., Sato Y., Imai A., and Tamaya T. Preterm labor and bacterial intra-amniotic infection: arachidonic acid liberation by phospholipase A2 of Prevotella bivia. Anaerobe 4 (1998) 209-212
21. Mikamo H., Sato Y., Hayasaki Y., et al. Intravaginal bacterial flora in patients with uterine cervical cancer. High incidence of detection of Gardnerella vaginalis. J Infect Chemother 5 (1999) 82-85
22. Sadhu K., Domingue P.A., Chow A.W., Nelligan J., Cheng N., and Costerton J.W. Gardnerella vaginalis has a gram-positive cell-wall ultrastructure and lacks classical cell-wall lipopolysaccharide. J Med Microbiol 29 (1989) 229-235
23. Greenwood J.R., and Pickett M.J. Salient features of Haemophilus vaginalis. J Clin Microbiol 9 (1979) 200-204
24. Sweet R.L. Role of bacterial vaginosis in pelvic inflammatory disease. Clin Infect Dis 20 Suppl 2 (1995) S271-S275
25. Boggess K.A., Watts D.H., Hillier S.L., Krohn M.A., Benedetti T.J., and Eschenbach D.A. Bacteremia shortly after placental separation during cesarean delivery. Obstet Gynecol 87 (1996) 779-784
26. Newton E.R., and Wallace P.A. Effects of prophylactic antibiotics on endometrial flora in women with postcesarean endometritis. Obstet Gynecol 92 (1998) 262-268
27. Cahill R.J., Tan S., Dougan G., et al. Universal DNA primers amplify bacterial DNA from human fetal membranes and link Fusobacterium nucleatum with prolonged preterm membrane rupture. Mol Hum Reprod 11 (2005) 761-766
28. Romero R., Gotsch F., Pineles B., and Kusanovic J.P. Inflammation in pregnancy: its roles in reproductive physiology, obstetrical complications, and fetal injury. Nutr Rev 65 (2007) S194-S202
29. Paul W. Fundamental immunology (1998), Lippincott-Raven, Philadelphia, PA
30. Mattsby-Baltzer I., Platz-Christensen J., Hosseini N., and Rosen P. IL I betta, IL 6, TNF alpha, fetal fibronectin, and endotoxin in the lower genital tract of pregnant women with bacterial vaginosis. Acta Obstet Gynecol Scand 77 (1998) 701-706
31. Platz-Christensen J.J., Mattsby-Baltzer I., Thomsen P., and Wiqvist N. Endotoxin and interleukin-1 alpha in the cervical mucus and vaginal fluid of pregnant women with bacterial vaginosis. Am J Obstet Gynecol 169 (1993) 1161-1166
32. Elovitz M.A., Wang Z., Chien E.K., Rychlik D.F., and Phillippe M. A new model for inflammation-induced preterm birth: the role of platelet-activating factor and Toll-like receptor-4. Am J Pathol 163 (2003) 2103-2111
33. Pillow J.J., Jobe A.H., Collins R.A., et al. Variability in preterm lamb lung mechanics after intra-amniotic endotoxin is associated with changes in surfactant pool size and morphometry. Am J Physiol Lung Cell Mol Physiol 287 (2004) L992-L998
34. Deb K., Chaturvedi M.M., and Jaiswal Y.K. Gram-negative bacterial LPS induced poor uterine receptivity and implantation failure in mouse: alterations in IL-1beta expression in the preimplantation embryo and uterine horns. Infect Dis Obstet Gynecol 13 (2005) 125-133
35. Newton E.R. The relationship between intrapartum obstetric care and chronic neurodevelopmental handicaps in children. Reprod Toxicol 4 (1990) 85-94
36. O'Shea T.M., Klinepeter K.L., Meis P.J., and Dillard R.G. Intrauterine infection and the risk of cerebral palsy in very low-birthweight infants. Paediatr Perinat Epidemiol 12 (1998) 72-83
37. Yoon B.H., Park C.W., and Chaiworapongsa T. Intrauterine infection and the development of cerebral palsy. Br J Obstet Gynaecol 110 Suppl 20 (2003) 124-127
38. Grether J.K., and Nelson K.B. Possible decrease in prevalence of cerebral palsy in premature infants. J Pediatr 136 (2000) 133
39. Eklind S., Mallard C., Leverin A.L., et al. Bacterial endotoxin sensitizes the immature brain to hypoxic-ischaemic injury. Eur J Neurosci 13 (2001) 1101-1106
40. Garnier Y., Coumans A.B., Jensen A., Hasaart T.H., and Berger R. Infection-related perinatal brain injury: the pathogenic role of impaired fetal cardiovascular control. J Soc Gynecol Invest 10 (2003) 450-459
41. Bell M.J., Hallenbeck J.M., and Gallo V. Determining the fetal inflammatory response in an experimental model of intrauterine inflammation in rats. Pediatr Res 56 (2004) 541-546
42. Bashiri A., Burstein E., and Mazor M. Cerebral palsy and fetal inflammatory response syndrome: a review. J Perinat Med 34 (2006) 5-12
43. Stolp H.B., Dziegielewska K.M., Ek C.J., Potter A.M., and Saunders N.R. Long-term changes in blood-brain barrier permeability and white matter following prolonged systemic inflammation in early development in the rat. Eur J Neurosci 22 (2005) 2805-2816
44. Svedin P., Kjellmer I., Welin A.K., Blad S., and Mallard C. Maturational effects of lipopolysaccharide on white-matter injury in fetal sheep. J Child Neurol 20 (2005) 960-964
45. Bell M.J., and Hallenbeck J.M. Effects of intrauterine inflammation on developing rat brain. J Neurosci Res 70 (2002) 570-579
46. Kannan S., Saadani-Makki F., Muzik O., et al. Microglial activation in perinatal rabbit brain induced by intrauterine inflammation: detection with 11C-(R)-PK11195 and small-animal PET. J Nucl Med 48 (2007) 946-954
47. Elovitz M.A., Mrinalini C., and Sammel M.D. Elucidating the early signal transduction pathways leading to fetal brain injury in preterm birth. Pediatr Res 59 (2006) 50-55
48. Sherwin C., and Fern R. Acute lipopolysaccharide-mediated injury in neonatal white matter glia: role of TNF-alpha, IL-1beta, and calcium. J Immunol 175 (2005) 155-161
49. Ling Z., Gayle D.A., Ma S.Y., et al. In utero bacterial endotoxin exposure causes loss of tyrosine hydroxylase neurons in the postnatal rat midbrain. Mov Disord 17 (2002) 116-124
50. Carvey P.M., Chang Q., Lipton J.W., and Ling Z. Prenatal exposure to the bacteriotoxin lipopolysaccharide leads to long-term losses of dopamine neurons in offspring: a potential, new model of Parkinson's disease. Front Biosci 8 (2003) s826-s837
51. Zhu Y., Carvey P.M., and Ling Z. Altered glutathione homeostasis in animals prenatally exposed to lipopolysaccharide. Neurochem Int 50 (2007) 671-680