Difference between revisions of "Group B Strep and Pregnancy"

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==Section 3==
 
==Section 3==
 
Whidbey et al. investigated how the GBS pigment induces cell lysis by measuring the kinetics of both K+ and hemoglobin (Hb) release from red blood cells treated with 400nM of the pigment<ref name=ww>[Whidbey, Christopher, et al. “A Streptococcal Lipid Toxin Induces Membrane Permeabilization and Pyroptosis Leading to Fetal&nbsp;Injury.” EMBO Molecular Medicine, vol. 7, no. 4, 2015, pp. 488–505., doi:10.15252/emmm.201404883.]</ref>. These results suggest that membrane permeabilization enables K+ and Hb to efflux, respectively. This delay in Hb suggests that the GBS pigment induces a colloidal osmotic mechanism of lysis rather than direct lysis<ref name=ww/>. Protection assays revealed that small osmoprotectants (e.g., PEG200) are incapable of protecting RBC from pigment-mediated hemolysis, whereas larger osmoprotectants (e.g, PEG1500) completely protect RBC from pigment-mediated hemolysis<ref name=ww/>. Interestingly, pigment-mediate membrane permeability is independent of cellular response, and it does not conform to a pore-forming protein toxin nor the induction of instant lysis<ref name=ww/>. 
 
Whidbey et al. investigated how the GBS pigment induces cell lysis by measuring the kinetics of both K+ and hemoglobin (Hb) release from red blood cells treated with 400nM of the pigment<ref name=ww>[Whidbey, Christopher, et al. “A Streptococcal Lipid Toxin Induces Membrane Permeabilization and Pyroptosis Leading to Fetal&nbsp;Injury.” EMBO Molecular Medicine, vol. 7, no. 4, 2015, pp. 488–505., doi:10.15252/emmm.201404883.]</ref>. These results suggest that membrane permeabilization enables K+ and Hb to efflux, respectively. This delay in Hb suggests that the GBS pigment induces a colloidal osmotic mechanism of lysis rather than direct lysis<ref name=ww/>. Protection assays revealed that small osmoprotectants (e.g., PEG200) are incapable of protecting RBC from pigment-mediated hemolysis, whereas larger osmoprotectants (e.g, PEG1500) completely protect RBC from pigment-mediated hemolysis<ref name=ww/>. Interestingly, pigment-mediate membrane permeability is independent of cellular response, and it does not conform to a pore-forming protein toxin nor the induction of instant lysis<ref name=ww/>. 
 +
 +
To further investigate the cytolytic abilities of GBS, researchers treated macrophages with various GBS strains (WT, ΔcovR, ΔcylE, and ΔcovRΔcylE) for four hours; cytotoxicity was measured by the release of lactate dehydrogenase<ref name=ww/>. Macrophage death and IL-1β release in cells that were infected with hyper-hemolytic GBS was significantly higher compared to those infected with non-hemolytic strains<ref name=ww/>. This, combined with further experiments that confirmed these findings and revealed an increase in IL-18 levels in macrophages treated with hyper-hemolytic GBS strains, suggest that the purified hemolytic GBS pigments is pro-inflammatory and cytotoxic<ref name=ww/>. 
  
 
==Section 4==
 
==Section 4==

Revision as of 07:09, 6 April 2021

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Introduction

This artistic recreation, based on scanning electron microscopy (SEM), depicts a three-dimensional (3D), computer-generated image, of a group of Gram-positive, Streptococcus agalactiae (group B Streptococcus) bacteria. Photo Credit: Alissa Eckert, who is a medical illustrator at the CDC.


By Shawn Ruiz


Group B Strep (GBS), also known as Streptococcus agalactiae, is a Gram-positive, beta-hemolytic, catalase-negative, facultative anaerobe that is a normal component of the gastrointestinal and genitourinary tracts[1]. In fact, GBS colonizes the gastrointestinal and genitourinary tracts of up to 50% of healthy adults[2]. Most healthy adults who are colonized by GBS will not experience any symptoms or GBS-related infections. While the bacteria is usually harmless in healthy adults, it is a major cause of meningitis, pneumonia, and and sepsis in neonates[3]. Moreover, GBS is the leading infectious cause of neonatal mortality and morbidity in the United States; between four and six percent of babies who develop GBS disease die[4][5]. GBS causes both early onset (<7 days old) and late onset (7-90 days old) infections in neonates[4]. The main risk factor for an early-onset GBS infection in a neonate is colonization of a birthing person's genital tract with Group B strep during labor[4]. About one in four pregnant individuals carry GBS in their body[5]. If the bacteria is present in a pregnant person, it can be directly transferred to their baby in a multitude of ways. For example, GBS can travel from the vagina into the amniotic fluid where the baby can ingest it. The baby can also come into contact with the bacteria as they make their way down the birth canal[3]. In the early 1990s, the early GBS infection rate was 1.7 cases per 1,000 births[3]. In an effort to decrease this infection rate, the American Congress of Obstetricians and Gynecologists and the American Academy of Pediatrics recommended screening pregnant individuals for GBS before they go into labor[3]. As a result, it is now common practice to screen pregnant individuals for GBS at some point between 35 and 37 weeks of pregnancy[5]. Pregnant people who test positive for GBS are treated with intravenous antibiotics during labor[5]. Penicillin and ampicillin are the recommended antibiotics for intrapartum GBS prophylaxis[6]. If a pregnant person tests positive for GBS and they are treated with antibiotics during labor, the risk of their neonate developing a serious, life-threatening GBS infection drops by 80% [3]. Early GBS infection rates in the United States have significantly dropped (0.25 cases per 1,000 births) since these preventative measures went into effect around 1995[3]. While intrapartum prophylaxis to prevent GBS transmission from the birthing individual to their neonate during labor and delivery has proven to be effective, this preventative measure does not target in utero infections that occur earlier in pregnancy, and little is known about the mechanisms that result in the infection of the amniotic cavity[7]. In utero GBS infections have devastating effects, including preterm birth and mortality in both the pregnant person and their baby[7]. That said, the it is critical that researchers and public health officials work toward understanding exactly how GBS infects the amniotic cavity.

Section 1

Figure 2. Primary hAECs were isolated from chorioamniotic membranes and the percent adherence of GBS WT, isogenic ΔcovR, ΔcovRΔcylE, and ΔcylE mutants were compared[7].[1].
Figure 3. Primary hAECs were isolated from chorioamniotic the percent invasion of GBS WT, isogenic ΔcovR, ΔcovRΔcylE, and ΔcylE mutants were compared[7]. [2].

GBS has been isolated from the amniotic fluid of birthing people with intact chorioamniotic membranes, suggesting that GBS is capable of invading and breaching amniotic epithelium and chorioamnion[7][8][9][10][11]. This led Whidbey et al. to hypothesize that “intra-amniotic GBS infections in patients with intact placenta or chorioamniotic membranes may be due to elevated virulence factor expression”[7][8][9][10][11].Previous studies showed that the expression of GBS virulence genes is regulated by a two-component regulatory system: COVR/S[7][12][13][14]. More specifically, COVR/S was described to repress a multitude of GBS virulence genes, including the cyl operon, which contains the cylE gene that is that is important for the production of the pluripotent toxin, hemolysin [7][12][13][14]. In order to test whether or not increased expression of GBS virulence genes promotes the invasion of amniotic epithelium, Whidbey et al. compared the abilities of wild-type (WT) GBS and hyper-hemolytic GBS (ΔcovR) GBS to adhere to and invade human amniotic epithelial cells (hAEC)[7].The hAECs were isolated and cultured from “normal, term placentas obtained immediately after cesarean delivery from” birthing people without labor[7]. Non-hemolytic GBS strains (ΔcovRΔcylE and ΔcylE) were also included in the experiment to investigate hemolysin’s role in GBS strains’ ability to adhere to and invade hAECs[7][15]. The results suggest that all GBS strains adhered to hAECs, as seen in Figure 2.Notably, as shown in Figure 3, WT GBS invaded hAECs (~4% invasion), non-hemolytic GBS showed a significantly decreased invasion when compared to the WT (~0.3% invasion), and the hyper-hemolytic strain (ΔcovR) was significantly more invasive when compared to the WT (~80% invasion)[7].In sum, Whidbey et al. concluded that hemolysin promotes GBS invasion of hAECs.


Next, Whidbey et al. investigated if the increased expression of hemolysin in the hyper-hemolytic GBS strain (ΔcovR) activates an inflammatory response[7]. Whidbey et al. isolated RNA from GBS-infected hAECs four hours after infection, and they used qRT-PCR to examine any changes in the expression of inflammatory genes[7][16]. The results, depicted in Figure 4, suggest that infection with ΔcovR caused a significant increase in the transcription of cytokines (e.g., IL-6 and IL-8) in hAECs[7]The increase in the expression of inflammatory genes in hAECS infected with ΔcovR was abolished in hAECs infected with the non-hemolytic strain, ΔcovRΔcylE. In sum, hAECs that were infected with the hyper-hemolytic GBS strain, ΔcovR, did show an inflammatory response. 

Figure 4. Whidbey et al. isolated RNA from hAECs infected with either WT GBS COH1 or isogenic ΔcovR, ΔcovRΔcylE, and ΔcylE mutants at 4 h after infection. qRT-PCR was performed on the RNA, and to examine the expression of cytokines/chemokines. "Data shown are the mean and SD obtained from hAECs that were isolated from three independent placentas, performed in triplicate (n = 3; **, P = 0.007; *, P = 0.03, Student’s t test, error bars ± SD)[7]."[3].


It is known that microbial toxins use the nuclear transcription factor, NF-𝜅B, which is recruited from the cytoplasm to the nucleus, to activate inflammatory signaling pathways[17]. Given that hAECs that were infected with ΔcovR showed an inflammatory response, Whidbey et al. investigated whether or not the increase in the expression of pro-inflammatory genes was associated with the nuclear recruitment/localization of NF-𝜅B[7].Whidbey et al. isolated total nuclear and cytoplasmic proteins from infected and uninfected hAECs, and they resolved them on 10% SDS-PAGE and Western blots[7]. As shown in Figure 5,hAECs that were infected with the hyper-hemolytic GBS strain (ΔcovR) showed a 2.5 fold increase in the nuclear recruitment of  NF-𝜅B[7].

Figure 5. Whidbey et al. performed Western Blots of nuclear and cytoplasmic proteins in GBS-infected hAECs(NF-𝜅B antibody). N and C stand for nuclear and cytoplasmic[7][4].


Despite finding that hemolysin is associated with an increase in the expression of pro-inflammatory genes, as well as the nuclear recruitment of NF-𝜅B, Whidbey et al. still did not know whether or not the presence of hemolysin accelerates the failure of the human amniotic epithelial barrier[7]. To examine this, Whidbey et al. monitored the changes in transepithelial electrical resistance across hAEC using electric cell-substrate impedance sensing[7][18]. Figure six shows that hAECs that were infected with the hyper-hemolytic strain (ΔcovR) showed an accelerated decrease in their barrier resistance compared to hAECs that were infected with WT GBS[7]. In sum, increased hemolysin expression decreased the barrier function of the amniotic epithelium, enabling GBS to breach the epithelial barrier[7].

Figure 6. Whidbey et al. used Electric Cell-substrate Impedance Sensing (ECIS) to monitor the barrier resistance of hAECs in real time.[5].


Knowing that an increase in hemolysin expression enabled hyper-hemolytic GBS to breach the hAEC epithelium, Whidbey et al. investigated whether or not GBS are capable of penetrating intact chorioamniotic membranes[7]. Whidbey et al. mounted, maintained, and, after 48 hours of stabilization, infected chorioamniotic membranes with various GBS strains (WT, ΔcovR, ΔcovRΔcylE). Figure 7 shows that only ΔcovR penetrated and invaded the chorioamnion, including the amniotic epithelium.This suggests that an increase in hemolysin expression can “facilitate bacterial penetration of chorioamniotic membranes and the amniotic cavity”[7].

Figure 7. GBS penetration of the chorion, amnion, and chorioamniotic membranes (n = 6; NS, P > 0.3; *, P = 0.02, Mann Whitney test, error bars ± SD)[7]."[6].


Considering that hyper-hemolytic GBS is capable of penetrating the chorioamniotic membranes and the amniotic cavity, resulting in an in-utero infection and preterm labor, Whidbey et al. hypothesized that increased hemolytic activity could be observed in GBS isolated from birthing people in preterm labor[7]. To test this hypothesis, they collected clinical isolates from amniotic fluid and chorioamnion from six birthing people in preterm labor[7]. These isolates were examined for potential mutations in the covR/S locus, as well as hemolytic properties. Eight GBS strains were obtained: most of them demonstrated increased hemolytic activity, and six of them had a mutation in the covR/S loci[7]. Notably, two GBS isolates did not have a mutation in the covR/S loci, but they did demonstrate increased hemolytic activity. That said, it is likely that hemolytic activity is regulated by multiple regulatory mechanisms. Site-directed mutations of the COVR/S mutations that were collected from clinical samples confirmed that the increase in hemolytic activity was in part attributable to these mutations[7].


One study suggested that the cylE gene, which is a part of the cyl operon, encoded and produced hemolysin[15]. Researchers proved, however, that while CylE is necessary for the production of hemolysin, it is not sufficient for GBS hemolysis. Notably, studies have shown that the hemolytic phenotype of GBS is pigmented and the non-hemolytic phenotype is not; this pigment is described as an ornithine rhamnolipid (i.e., granadaene)[15][19][20]. Like hemolytic activity, pigment biosynthesis in GBS also requires the cyl open Whidbey et al. conducted a sequence profile analysis of CylE, which they used in combination with predicted homology profiles, to propose a pathway (depicted in Figure 9) for GBS pigment biosynthesis that is dependent on the majority of genes in the cyl operon[7].


Whidbey et al. propose that the ornithine rhamnolipid pigment, rather than the CylE protein, is the cause of the hemolytic activity in GBS. To test this, they extracted and purified pigment from WT GBS and examined the hemolytic activity of the pigment. Lysis of red blood cells occurred in the presence of the pigment, and brief (8 min) exposure to the pigment dramatically altered the membrane morphology of the disc-shaped red blood cells, as shown in Figure 10. Researchers confirmed that the hemolytic activity observed in the lysis of red blood cells could not be attributed to a protein toxin by demonstrating that the purified pigment was not affected by proteinase K. Other conformational experiments, such as SDS-PAGE analysis of the purified pigment, were also performed[7].

Figure 9.Proposed pathway for the biosynthesis of the GBS pigment, granadaene[7].[7].
Figure 10.Scanning electron micrographs of hRBCs 8 minutes after exposure to GBS pigment (12.5 µM), buffer or ΔcylE extract.[7].[8].

Section 3

Whidbey et al. investigated how the GBS pigment induces cell lysis by measuring the kinetics of both K+ and hemoglobin (Hb) release from red blood cells treated with 400nM of the pigment[21]. These results suggest that membrane permeabilization enables K+ and Hb to efflux, respectively. This delay in Hb suggests that the GBS pigment induces a colloidal osmotic mechanism of lysis rather than direct lysis[21]. Protection assays revealed that small osmoprotectants (e.g., PEG200) are incapable of protecting RBC from pigment-mediated hemolysis, whereas larger osmoprotectants (e.g, PEG1500) completely protect RBC from pigment-mediated hemolysis[21]. Interestingly, pigment-mediate membrane permeability is independent of cellular response, and it does not conform to a pore-forming protein toxin nor the induction of instant lysis[21]

To further investigate the cytolytic abilities of GBS, researchers treated macrophages with various GBS strains (WT, ΔcovR, ΔcylE, and ΔcovRΔcylE) for four hours; cytotoxicity was measured by the release of lactate dehydrogenase[21]. Macrophage death and IL-1β release in cells that were infected with hyper-hemolytic GBS was significantly higher compared to those infected with non-hemolytic strains[21]. This, combined with further experiments that confirmed these findings and revealed an increase in IL-18 levels in macrophages treated with hyper-hemolytic GBS strains, suggest that the purified hemolytic GBS pigments is pro-inflammatory and cytotoxic[21]

Section 4

Conclusion

References



Authored for BIOL 238 Microbiology, taught by Joan Slonczewski, 2021, Kenyon College.

  1. [“Streptococcus Agalactiae.” Wikipedia, Wikimedia Foundation, 24 Mar. 2021, en.wikipedia.org/wiki/Streptococcus_agalactiae.].
  2. [Johri, Atul Kumar, et al. “Group B Streptococcus: Global Incidence and Vaccine Development.” Nature Reviews Microbiology, vol. 4, no. 12, 2006, pp. 932–942., doi:10.1038/nrmicro1552.].
  3. 3.0 3.1 3.2 3.3 3.4 3.5 [Dekker, Rebecca. “The Evidence on: Group B Strep.” Evidence Based Birth , Evidence Based Birth , 17 July 2017, evidencebasedbirth.com/groupbstrep/.].
  4. 4.0 4.1 4.2 [Morgan, John A. “Group B Streptococcus And Pregnancy.” StatPearls [Internet]., U.S. National Library of Medicine, 29 Jan. 2021, www.ncbi.nlm.nih.gov/books/NBK482443/#:~:text=Preterm%20infants%20with%20early%2Donset,in%20term%20infants%5B2%5D.]
  5. 5.0 5.1 5.2 5.3 [“Group B Strep: Fast Facts and Statistics.” Centers for Disease Control and Prevention, Centers for Disease Control and Prevention, 11 June 2020, www.cdc.gov/groupbstrep/about/fast-facts.html#references.]
  6. [Horsley, Elizabeth. “CDC Updates Guidelines for the Prevention of Perinatal GBS Disease.” American Family Physician, The American Academy of Family Physicians Foundation , 1 May 2011, www.aafp.org/afp/2011/0501/p1106.html#:~:text=The%20recommended%20antibiotic%20for%20intrapartum,units%20intravenously%20every%20four%20hours.]
  7. 7.00 7.01 7.02 7.03 7.04 7.05 7.06 7.07 7.08 7.09 7.10 7.11 7.12 7.13 7.14 7.15 7.16 7.17 7.18 7.19 7.20 7.21 7.22 7.23 7.24 7.25 7.26 7.27 7.28 7.29 7.30 7.31 7.32 7.33 7.34 [Whidbey, Christopher, et al. “A Hemolytic Pigment of Group B Streptococcus Allows Bacterial Penetration of Human Placenta.” Journal of Experimental Medicine, vol. 210, no. 6, 2013, pp. 1265–1281., doi:10.1084/jem.20122753.]
  8. 8.0 8.1 [JR, Bobitt, and Ledger WJ. “Unrecognized Amnionitis and Prematurity: a Preliminary Report.” The Journal of Reproductive Medicine., vol. 19, no. 1, 30 June 1977, pp. 8–12., europepmc.org/article/med/874942.]
  9. 9.0 9.1 [Naeye , RL, and EC Peters. “Amniotic Fluid Infections with Intact Membranes Leading to Perinatal Death: a Prospective Study.” Pediatrics, U.S. National Library of Medicine, Feb. 1978, pubmed.ncbi.nlm.nih.gov/634667/.]
  10. 10.0 10.1 [Winram, Scott B., et al. “Characterization of Group B Streptococcal Invasion of Human Chorion and Amnion Epithelial Cells In Vitro.” Infection and Immunity, vol. 66, no. 10, 1998, pp. 4932–4941., doi:10.1128/iai.66.10.4932-4941.1998.]
  11. 11.0 11.1 [Goldenberg, Robert L., et al. “Intrauterine Infection and Preterm Delivery.” New England Journal of Medicine, vol. 342, no. 20, 2000, pp. 1500–1507., doi:10.1056/nejm200005183422007.]
  12. 12.0 12.1 [Lamy, Marie-Cécile, et al. “CovS/CovR of Group B Streptococcus: a Two-Component Global Regulatory System Involved in Virulence.” Molecular Microbiology, vol. 54, no. 5, 2004, pp. 1250–1268., doi:10.1111/j.1365-2958.2004.04365.x.]
  13. 13.0 13.1 [Jiang, Sheng-Mei, et al. “Variation in the Group B Streptococcus CsrRS Regulon and Effects on Pathogenicity.” Journal of Bacteriology, vol. 190, no. 6, 2008, pp. 1956–1965., doi:10.1128/jb.01677-07.]
  14. 14.0 14.1 [Rajagopal, Lakshmi, et al. “Regulation of Cytotoxin Expression by Converging Eukaryotic-Type and Two-Component Signalling Mechanisms in Streptococcus Agalactiae.” Molecular Microbiology, vol. 62, no. 4, 2006, pp. 941–957., doi:10.1111/j.1365-2958.2006.05431.x.]
  15. 15.0 15.1 15.2 [Pritzlaff, Craig A., et al. “Genetic Basis for the Beta-Haemolytic/Cytolytic Activity of Group B Streptococcus.” Molecular Microbiology, vol. 39, no. 2, 2001, pp. 236–248., doi:10.1046/j.1365-2958.2001.02211.x.]
  16. [Lembo, Annalisa, et al. “Regulation of CovR Expression in Group B Streptococcus Impacts Blood-Brain Barrier Penetration.” Molecular Microbiology, vol. 77, no. 2, 2010, pp. 431–443., doi:10.1111/j.1365-2958.2010.07215.x.]
  17. [Gonzalez, M. R., et al. “Bacterial Pore-Forming Toxins: The (w)Hole Story?” Cellular and Molecular Life Sciences, vol. 65, no. 3, 2007, pp. 493–507., doi:10.1007/s00018-007-7434-y. ]
  18. [Giaever, I., and C. R. Keese. “Micromotion of Mammalian Cells Measured Electrically.” Proceedings of the National Academy of Sciences, vol. 88, no. 17, 1991, pp. 7896–7900., doi:10.1073/pnas.88.17.7896.]
  19. [Nizet, V, et al. “Group B Streptococcal Beta-Hemolysin Expression Is Associated with Injury of Lung Epithelial Cells.” Infection and Immunity, vol. 64, no. 9, 1996, pp. 3818–3826., doi:10.1128/iai.64.9.3818-3826.1996.]
  20. [Spellerberg, Barbara, et al. “Thecylgenes OfStreptococcus Agalactiaeare Involved in the Production of Pigment.” FEMS Microbiology Letters, vol. 188, no. 2, 2000, pp. 125–128., doi:10.1111/j.1574-6968.2000.tb09182.x.]
  21. 21.0 21.1 21.2 21.3 21.4 21.5 21.6 [Whidbey, Christopher, et al. “A Streptococcal Lipid Toxin Induces Membrane Permeabilization and Pyroptosis Leading to Fetal Injury.” EMBO Molecular Medicine, vol. 7, no. 4, 2015, pp. 488–505., doi:10.15252/emmm.201404883.]