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group_3_presentation_1_-_zika_virus [2018/02/02 14:52] duruf [Zika Virus Preclinical Studies] |
group_3_presentation_1_-_zika_virus [2018/02/02 14:55] (current) duruf [Microcephaly] |
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| Guillain-Barre Syndrome (GBS) is a rare autoimmune disease that affects neurons. Specifically, the myelin coating around axons is damaged and the conduction of signals between nerve cells is compromised. | Guillain-Barre Syndrome (GBS) is a rare autoimmune disease that affects neurons. Specifically, the myelin coating around axons is damaged and the conduction of signals between nerve cells is compromised. | ||
| - | A recent study by Cao-Lormeau et al. (2016) published in //The Lancet// presented considerable evidence linking GBS with previous Zika virus infection. The researchers presented a case study involving 42 individuals with confirmed GBS during a massive Zika virus outbreak in French Polynesia between 2013 and 2014. Blood samples were taken from patients with confirmed GBS (n=42) and patients without GBS (control; n=98). The researchers used various techniques to detect antibodies against Zika virus (IgM/IgG) in both groups of patients. Evidence of previous Zika virus infection, demonstrated by the presence of Zika antibodies, was shown for 41 (98%) patients in the GBS group compared to 35 (36%) of patients in the control group (Figure 3; p<0.0001). In addition, a neutralizing response against Zika virus was seen in 42 (100%) of the GBS patients and 54 (56%) of the control group patients (Figure 3; p<0.0001). This data presented by Cao-Lormeau et al. (2016) exhibits a significant association between previous Zika virus infection and GBS. | + | A recent study by Cao-Lormeau et al. (2016) published in //The Lancet// presented considerable evidence linking GBS with previous Zika virus infection. The researchers presented a case study involving 42 individuals with confirmed GBS during a massive Zika virus outbreak in French Polynesia between 2013 and 2014. Blood samples were taken from patients with confirmed GBS (n=42) and patients without GBS (control; n=98). The researchers used various techniques to detect antibodies against Zika virus (IgM/IgG) in both groups of patients. Evidence of previous Zika virus infection, demonstrated by the presence of Zika antibodies, was shown for 41 (98%) patients in the GBS group compared to 35 (36%) of patients in the control group (Figure 5; p<0.0001). In addition, a neutralizing response against Zika virus was seen in 42 (100%) of the GBS patients and 54 (56%) of the control group patients (Figure 5; p<0.0001). This data presented by Cao-Lormeau et al. (2016) exhibits a significant association between previous Zika virus infection and GBS. |
| <box 57% round | > {{:gbs_cao.png?625|}} </box| Figure 5 : Presence of Zika virus antibodies and positive neutralizing response in GBS affected and control patients. OR= Odds Ratio. (Modified from Cao-Lormeau et al., 2016)> | <box 57% round | > {{:gbs_cao.png?625|}} </box| Figure 5 : Presence of Zika virus antibodies and positive neutralizing response in GBS affected and control patients. OR= Odds Ratio. (Modified from Cao-Lormeau et al., 2016)> | ||
| ==== Microcephaly ==== | ==== Microcephaly ==== | ||
| - | Microcephaly is a birth defect associated with Congenital Zika Syndrome. Babies with microcephaly have a smaller head circumference than age and sex-matched patients. The decreased head circumference is due to improper or lack of brain development during pregnancy (CDC, 2018). Severe microcephaly (Figure 4) is an extreme form of the condition where the baby's head circumference is much smaller (~1st percentile) than babies of the same age and sex (~3rd percentile) (CDC, 2018). | + | Microcephaly is a birth defect associated with Congenital Zika Syndrome. Babies with microcephaly have a smaller head circumference than age and sex-matched patients. The decreased head circumference is due to improper or lack of brain development during pregnancy (CDC, 2018). Severe microcephaly (Figure 6) is an extreme form of the condition where the baby's head circumference is much smaller (~1st percentile) than babies of the same age and sex (~3rd percentile) (CDC, 2018). |
| <box 58% round| > {{::microcephaly_screen_shot_2018-01-24_at_11.19.55_am.png?625|}} </box| Figure 6: Baby with normal head circumference, microcephaly, and severe microcephaly, respectively (Modified from CDC, 2018)> | <box 58% round| > {{::microcephaly_screen_shot_2018-01-24_at_11.19.55_am.png?625|}} </box| Figure 6: Baby with normal head circumference, microcephaly, and severe microcephaly, respectively (Modified from CDC, 2018)> | ||
| - | A case study published by Mlakar et al. (2016) in //The New England Journal of Medicine// described the morphology of a baby with confirmed severe microcephaly. The mother, who had been infected with Zika virus, requested termination of the pregnancy at 32 weeks. At the time of termination the fetus' head circumference was 26cm (1st percentile). An autopsy performed on the fetal brain showed clear degeneration, calcifications, malformation and incomplete development of important structures (Figure 5), resulting in the small head circumference characteristic of microcephaly. | + | A case study published by Mlakar et al. (2016) in //The New England Journal of Medicine// described the morphology of a baby with confirmed severe microcephaly. The mother, who had been infected with Zika virus, requested termination of the pregnancy at 32 weeks. At the time of termination the fetus' head circumference was 26cm (1st percentile). An autopsy performed on the fetal brain showed clear degeneration, calcifications, malformation and incomplete development of important structures (Figure 7), resulting in the small head circumference characteristic of microcephaly. |
| <box 58% round| > {{:fetal_autopsy_brain.png?625|}} </box| Figure 7: Autopsy of fetal brain. Panel C shows white calcifications and loss of gyration in cortex (Black arrows), open sylvian fissures (Black arrowheads), and poorly delineated basal ganglia (Black asterisks). Panel D shows dilated lateral ventricles and collapsed left ventricle (White arrowheads), thalami are well developed (Black asterisks) along with the hippocampus (White asterisks), however contralateral structure failed to develop. (Modified from Mlakar et al., 2016)> | <box 58% round| > {{:fetal_autopsy_brain.png?625|}} </box| Figure 7: Autopsy of fetal brain. Panel C shows white calcifications and loss of gyration in cortex (Black arrows), open sylvian fissures (Black arrowheads), and poorly delineated basal ganglia (Black asterisks). Panel D shows dilated lateral ventricles and collapsed left ventricle (White arrowheads), thalami are well developed (Black asterisks) along with the hippocampus (White asterisks), however contralateral structure failed to develop. (Modified from Mlakar et al., 2016)> | ||
| - | In addition, Mlakar et al. (2016) used electron microscopy to image ultra-thin sections of the fetal brain and staining of viral particles in order to visualize the presence of Zika virus in the fetal brain tissue. Imaging showed dense clusters of viral particles among the damaged brain tissue, as well as the presence of active viral replication (Figure 6). | + | In addition, Mlakar et al. (2016) used electron microscopy to image ultra-thin sections of the fetal brain and staining of viral particles in order to visualize the presence of Zika virus in the fetal brain tissue. Imaging showed dense clusters of viral particles among the damaged brain tissue, as well as the presence of active viral replication (Figure 8). |
| <box 45% round| > {{:electron_microscopy.png?475|}} </box| Figure 8: Electron microscopy of ultra-thin sections of the fetal brain and staining of viral particles. Panel A shows dense clusters of virions amongst damaged brain cells. Panel B is a magnified image of Panel A, clearly showing the virion clusters. Panel C shows viral particles with bright interiors indicative of viral replication. Panel D is a negative staining of a virion showing morphological characteristics consistent with Zika virus (Modified from Mlakar et al., 2016)> | <box 45% round| > {{:electron_microscopy.png?475|}} </box| Figure 8: Electron microscopy of ultra-thin sections of the fetal brain and staining of viral particles. Panel A shows dense clusters of virions amongst damaged brain cells. Panel B is a magnified image of Panel A, clearly showing the virion clusters. Panel C shows viral particles with bright interiors indicative of viral replication. Panel D is a negative staining of a virion showing morphological characteristics consistent with Zika virus (Modified from Mlakar et al., 2016)> | ||
