Hepatitis B and Hepatitis D virus

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Hepatitis B and Hepatitis D virus

Block 9 Gastrointestinal partial

Block 9 Gastrointestinal partial

Colon histology
Esophagus histology
Gallbladder histology
Liver histology
Pancreas histology
Small intestine histology
Stomach histology
Gastroesophageal reflux disease (GERD)
Barrett esophagus
Eosinophilic esophagitis (NORD)
Esophageal cancer
Mallory-Weiss syndrome
Esophageal atresia and tracheoesophageal fistula: Year of the Zebra
Achalasia
Achalasia: Year of the Zebra
Esophageal disorders: Clinical
Esophageal disorders: Pathology review
Esophagitis: Clinical
Gastroesophageal reflux disease (GERD): Clinical
Gastroesophageal reflux disease: Clinical sciences
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Plummer-Vinson syndrome
Gastrointestinal bleeding: Clinical
Gastrointestinal bleeding: Pathology review
Diffuse esophageal spasm
Scleroderma: Pathology review
Scleroderma
Boerhaave syndrome
Pediatric gastrointestinal bleeding: Clinical
Jaundice
Jaundice: Pathology review
Jaundice: Clinical
Neonatal jaundice: Clinical
Approach to jaundice (unconjugated hyperbilirubinemia): Clinical sciences
Approach to jaundice (conjugated hyperbilirubinemia): Clinical sciences
Cholestatic liver disease
Cirrhosis: Clinical
Hepatitis B and Hepatitis D virus
Viral hepatitis: Pathology review
Viral hepatitis: Clinical
Viral hepatitis
Cirrhosis
Cirrhosis: Clinical sciences
Cirrhosis: Pathology review
Portal hypertension
Pulmonary arterial hypertension (NORD)
Approach to ascites: Clinical sciences
Pancreatitis: Clinical
Hepatocellular carcinoma
Hepatocellular adenoma
Peptic ulcer
Peptic ulcer disease: Clinical sciences
Peptic ulcers and stomach cancer: Clinical
Zollinger-Ellison syndrome
Approach to melena and hematemesis: Clinical sciences
Acid reducing medications
Antidiarrheals
Acute pancreatitis
Pancreatitis: Pathology review
Chronic pancreatitis
Chronic pancreatitis: Clinical sciences
Pancreatic cancer
Pancreatic cancer: Clinical sciences
Pancreatic neuroendocrine neoplasms
Acute cholecystitis
Neuroendocrine tumors of the gastrointestinal system: Pathology review
MEN syndromes: Clinical
Multiple endocrine neoplasia: Pathology review
Diabetes mellitus: Clinical
Diabetes mellitus
Diabetes mellitus: Pathology review
Diabetes mellitus (Type 2): Clinical sciences
Bowel obstruction: Clinical
Bowel obstruction
Large bowel obstruction: Clinical sciences
Small bowel obstruction: Clinical sciences
Irritable bowel syndrome
Inflammatory bowel disease: Pathology review
Inflammatory bowel disease: Clinical
Inflammatory bowel disease (Crohn disease): Clinical sciences
Short bowel syndrome (NORD)
Small bowel ischemia and infarction
Inflammatory bowel disease (ulcerative colitis): Clinical sciences
Diverticular disease: Clinical
Abdominal hernias
Hernias: Clinical
Inguinal hernia
Abdominal trauma: Clinical
Intussusception
Rotavirus
Congenital gastrointestinal disorders: Pathology review
Intestinal atresia
Diarrhea: Clinical
Yersinia enterocolitica
Escherichia coli
Malabsorption: Clinical
Malabsorption syndromes: Pathology review
Celiac disease
Tropical sprue
Whipple's disease
Colorectal polyps and cancer: Pathology review
Diverticular disease: Pathology review
Gallbladder disorders: Pathology review
Biliary atresia
Crigler-Najjar syndrome
Gilbert's syndrome
Gallstone ileus
Colorectal cancer
Colorectal polyps
Femoral hernia
Crohn disease
Ulcerative colitis
Microscopic colitis
Ischemic colitis
Carcinoid syndrome
Diverticulosis and diverticulitis
Gastroenteritis
Zenker diverticulum
Gastritis
Gastric cancer
Gastric dumping syndrome
Oral candidiasis
Oral cancer
Norovirus
Anal fissure
Anal fistula
Anal fissure: Clinical sciences

Transcript

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Hepatitis B virus, or Hep B virus for short, is a member of the hepadnavirus family; hepatitis D virus, or Hep D virus, is a deltavirus. They both cause hepatitis, or inflammation of the liver. Even though they both cause hepatitis, hepatitis D virus cannot cause the disease by itself, and needs hepatitis B virus to replicate.  

Both hep B and D viruses are enveloped, so they’re surrounded by a membrane. To make things interesting, the membrane of both viruses contains hepatitis B viral proteins - specifically, they both have a surface antigen called HBs. Beneath the membrane there is a protein shell called a capsid, which has more antigens. HB core, or HBc, is in the capsid of hepatitis B. There is also an HB envelope or HBe antigen for short, which is a variant of HBc but it’s not really part of the virus. It’s secreted, and can be found in infected individuals' serum. Delta antigen or HDAg for short is in the capsid of hepatitis D virus. 

Inside the capsid, there’s the viral genetic material. Now, hep B is a DNA virus, which means that its capsid contains partial double-stranded circular DNA, which is made of a long and short strand, so there is a part where the long strand is single stranded. And it also has DNA polymerase, which is an enzyme with DNA- and RNA-dependent activity, meaning it can convert DNA to RNA and vice versa. On the other hand, hep D is an RNA virus, so its capsid contains single-stranded circular RNA in a rod-like folded structure, which is why host cell enzymes can use it as double-stranded DNA.

The main source of hepatitis B virus is blood, but it can also be found in other bodily fluids like milk, amniotic fluid, vaginal secretions and semen. So, routes of transmission include: sexual contact; contaminated blood, either following transfusions or injections with contaminated needles, the latter being more common in people who use intravenous drugs. The virus can also be passed from an infected mother to the baby during childbirth. Rarely, during the pregnancy the virus can pass through the placental barrier, which is a kind of a very thin wall that brings the mother’s and fetus' blood very close, and allows them to exchange some substances like oxygen, IgG antibodies, waste products and unfortunately certain microbes. More commonly the virus can pass from an infected individual to the child during birth because of the close contact between the individual's blood and secretions with the child. It is still not certain if C section can protect against this kind of transmission. Hepatitis D virus spreads the same way, but it only causes disease in individuals with an active hepatitis B infection.

Alright, now, both these viruses target the liver, which is made of functional units called hepatic lobules. The main cells are called hepatocytes. They pick up and detoxify harmful substances like drugs or alcohol; help maintain a normal blood glucose level; synthesize a variety of important proteins, like albumin and coagulation factors; store certain vitamins and some minerals; and convert cholesterol into bile salts, which, along with water and bilirubin, make up the bile.

Hepatitis B virus enters the hepatocytes by fusing its membrane with the cell membrane and releasing the capsid into the cell. The cell's polymerase elongates the shorter strand of the viral DNA, so that it now forms a complete double-stranded DNA with the long strand. It then travels to the nucleus. There, it is transcribed by the cell's transcription elements into multiple mRNAs, which leave the nucleus and use the cell’s ribosomes to create viral proteins, like DNA polymerase and viral antigens: HBs, HB core and HBe antigen. The largest mRNA is used by the viral DNA polymerase to replicate viral DNA.  Viral antigens Hbs and Hb core are assembled into new viral particles. Hbe, however, isn’t included in the viral particle, but leaves the cell and can be found in the serum. The viral DNA is replicated and packaged into capsid at the same time, which is why its replication is interrupted and the virus gets partial double-stranded DNA. The capsid is then enveloped and released without damaging the cell, which is why the infection can persist for a long time without causing liver damage

The damage actually comes from the body's immune system. T-cells find and eliminate infected hepatocytes, which causes liver damage. B-cells react to the virus in the bloodstream and secrete antibodies against hep B antigens. Bilirubin with bile salts is released from the destroyed cells into the bloodstream and impregnates the tissue, causing jaundice, which is a yellowish pigmentation of the skin, mucosa and whites of the eyes. The bile salts get into the skin, and cause itching. The bilirubin from the blood is filtered by the kidneys and ends up in the urine instead of the stool, making it dark, while the stool becomes pale.

An insufficient T-cell response, or, if large amounts of HBs antigen bind to neutralizing antibodies, it can lead to chronic hepatitis. Acute hepatitis B becomes chronic in about 5 to 10% of cases. In some cases, liver damage can progress to scarring, cirrhosis and liver failure. Chronic hepatitis also increases the risk of liver cancer called hepatocellular carcinoma.

Hepatitis D virus enters the cell and the nucleus in the same way. However, it uses the host cell’s RNA polymerase to copy itself and the cell's ribosomes to create delta antigens. Viral RNA is packaged into the capsid, but in order to make a complete viral particle it must use HBs antigen and get enveloped. It then leaves the cell.

Now, delta antigens are harmful to the cell and cause cell death and liver damage, so unlike hep B, hep D damages the cells directly.

Hep D virus causes acute hepatitis in one of two ways. First, there’s co-infection with hep B, when the two viruses infect the liver at the same time; second, there’s superinfection, which is when hep D infects individuals with chronic hepatitis B, which is more severe. Hep D increases the severity of the hep B infection. These individuals are more likely to develop fulminant hepatitis, massive liver necrosis, and hepatic encephalopathy, when the brain function is affected.