INFECTIOUS DISEASE

VIROLOGY - CHAPTER SEVENTEEN

VIRAL AGENTS OF GASTROENTERITIS

ROTAVIRUSES, CALICIVIRUSES, ADENOVIRUSES, ASTROVIRUSES AND OTHERS

Dr N. Narayan and Dr Helmut Albrecht

Figure 1. Rotavirus (A double-capsid particle (left), and a single, inner, capsid (right)) © Dr Linda Stannard, University of Cape Town, South Africa

• Rotaviruses
• Adenoviruses 40/41
• Caliciviruses
• Norwalk-like viruses or small round structured viruses (SRSV)
• Astroviruses
• Small round viruses (SRV)
• Coronaviruses
• Toroviruses

Other viruses found in the gut of a normal individual are not normally associated with gastroenteritis

• Poliovirus
• Coxsackie A virus
• Coxsackie B Virus
• Echoviruses
• Enteroviruses 68-71
• Hepatitis A virus
• Hepatitis E virus
• Adenoviruses 1-39
• Reoviruses

Others are found in the gut as opportunistic infections

• Cytomegalovirus (CMV)
• Herpes simplex virus (HSV)
• Human immunodeficiency virus (HIV)

ROTAVIRUSES

Classification

The family Reoviridae includes the genus Rotavirus and Coltivirus (includes Colorado Tick Fever virus). Other genera include the Orthreoviruses and Orbiviruses (found in sheep).

Rotavirus was first identified by electron microscopy in 1973 from duodenal biopsies of children with diarrhea. Human and animal rotaviruses are known.

Structure

Rotaviruses are non-enveloped viruses with icosahedral symmetry and a double capsid (figure 1). Their electron microscopic appearance shows a 60-80nm wheel with radiating spokes (Latin, rota = wheel) (figure 2).

The rotavirus genome contains double stranded (ds) RNA in 11 segments that can be separated by polyacrylamide gel electrophoresis (PAGE).

Major structural proteins

Outer structural proteins are VP7 and VP4. VP4 is the viral hemagglutinin and forms spikes from the surface.

Inner core structural proteins are VP 1, 2, 3, and 6. VP6 is an important antigenic determinant.
 

Classification

Groups

There are seven different groups (A to G) based on the antigenicity (each group shares common antigens) and the electrophoretic mobility of their RNA segments. Groups D, E and F have not been found in humans.  Group A is the most common and only group A rotaviruses cause human disease  in the United States, primarily in the young (under two years of age - infantile gastroenteritis). However, group A rotaviruses can also cause milder diarrhea in older children and adults. Group B has been found to cause human disease in China where there may be annual outbreaks of severe adult and infant diarrhea. More characteristically, group B rotaviruses cause diarrhea in pigs. Group C is found worldwide.

Serotypes 

There are at least 15 different serotypes of rotaviruses.  Fourteen G serotypes are based on G protein (GP7) differences. Five predominant strains in the United States (G1, G2, G3, G4, G9) account for 90% of isolates and strain G1 accounts for 73% of infections.

There are 20 P serotypes based on the P protein (VP4) with P4 and P8 predominating.

Common P/G combinations are P8G1, P8G2, P4G2 and P8G4
 

Properties

Rotaviruses are stable in the environment for many months and are relative resistant to hand washing. They are susceptible to agents such as 95% ethanol,  formalin and "Lysol". They are also unstable to pH below 2.

WEB RESOURCES

Rotavirus structure
(Dr LInda Stannard)

Gastroenteritis Fact Sheet
CDC 

Rotavirus Diarrhea in the Child Care Setting
CDC

Rotavirus
CDC pdf file

 

Figure 2. Transmission electron micrograph of intact rotavirus particles, double-shelled. Distinctive rim of radiating capsomeres. CDC/Dr. Erskine Palmer 

Pathogenesis

Affected host cells are mature enterocytes lining the middle and upper end of the intestinal villi. In laboratory animals, hepatocytes are also infected. The infectious particle is thought to be an "intermediate sub-viral particle" (ISVP).

The viral attachment protein is probably exposed after protease digestion in the GI tract removes some or all of the outer capsid protein (VP4). Rotaviruses replicate in the host cell cytoplasm. Virions enter the host cell by endocytosis and viral mRNA is transcribed using the viral RNA polymerase that is already present in the virion to form structural protein units of the capsid. The mRNA segments are assembled into the immature capsid and then replicated to form the double stranded RNA genome. Large amounts of viral particles are shed in diarrheal stools.

Histopathology of infected intestines shows villous atrophy and blunting, due to death of the mature enterocytes and infiltration of lamina propria with mononuclear cells. Subsequently there is repopulation of the villous tips with immature secretory cells (crypt hyperplasia).

Cell dysfunction and death results in a net secretion of intestinal fluid, hence the watery diarrhea. Activation of the enteric nervous system may also play a role.

Repopulation with immature secretory cells may contribute to the secondary lactose intolerance that is sometimes seen.

Figure 3. Estimated global distribution of the 800,000 annual deaths caused by rotavirus diarrhea.  CDC

Figure 4. Average time of peak rotavirus activity in the contiguous 48 states, United States, July 1991 to June 1997  CDC

Figure 5. Month of peak rotavirus activity — United States, July 1996–June 1997

Figure 6. Average time of peak rotavirus activity in the contiguous 48 states, United States, July 1991 to June 1992. This contour plot was derived using the median value for time of peak activity for each laboratory. CDC

Higher resolution movie of above image avi file

Peak month for reports of rotavirus infections across the US, 1991-97
avi file

Weekly reports of rotavirus in the US. Seasonal variation. CDC

Epidemiology

Distribution
Rotaviruses are found worldwide, causing major diarrhea-associated hospitalization and 600,000-850,000 deaths per year (figure 3). Seroprevalence studies show that antibody is present in most infants by age 3 years.

In the U.S., there are 20 - 40 deaths per year with 50-70,000 hospitalizations and 500,000 physician visits per year. In about 1-2.5% of case there is severe dehydration. In all, there are probably about 2.7 to 3.5 million people in the US affected by rotavirus infections each year.

Seasonality

In the U.S.A., rotavirus infections occur in the winter months (November through May). The disease spreads across North America from the warmer climates, starting from Mexico and SW USA and gradually progressing N/NE to reach East Coast and Canada in spring (figures 4 - 6). As might be expected, rotavirus infections are seen year round in the tropics.

Incubation period
This is thought to be less than 4 days

Contagious Period
The patient is contagious from before the onset of diarrhea to a few days after the end of diarrhea.

Age of infections
Rotaviruses infect children at a young age. Older infants and young children (4 months - 2 years) tend to be more symptomatic with diarrhea. Young infants may be protected due to trans-placental transfer of antibody. Asymptomatic infections are common, especially in adults. Many cases and outbreaks are nosocomial

Group A infections are most common.

Group B has been associated with outbreaks in adults in China

Group C is responsible for sporadic cases of diarrhea in infants around the world.

Spread is mainly person to person via fecal - oral route and through fomites. Spread by food and water is also possible. Ther has been speculation that rotaviruses may also spread via the respiratory route.

High numbers of viral particles are shed in diarrheal stools (10¹⁰/gm). Infective dose is only 10-100 pfu.

Clinical Features

Fever can be high grade (>102° F in 30% of patients) and vomiting and nausea precedes diarrhea. Diarrhea is usually watery (no blood or leukocytes), lasting 3-9 days, but longer in malnourished and immune deficient individuals. Necrotizing enterocolitis and hemorrhagic gastroenteritis is seen in neonates. Dehydration is the main contributor to mortality. Secondary malabsorption of lactose and fat, and chronic diarrhea are possible.
 

Diagnosis

Rapid diagnosis can be obtained by antigen detection in stool using ELISA (which uses a monoclonal antibody) and LA. Several kits are commercially available. These detect only Group A rotavirus. Electron microscopy also detects non-Group A viruses.

Group A rotaviruses can be cultured in monkey kidney cells.

Epidemiologic studies use patterns of viral RNA migration by gel electrophoresis (electropherotyping). Different genetic strains may circulate in a given community.
 

Treatment

Treatment is just supportive care with rehydration (oral / intravenous). Antiviral agents not known to be effective
 

Prevention of spread

Good hand washing technique is important. In addition, surfaces, toilets and toys should be disinfected. Adequate chlorination of water can prevent spread in the community.

Immunity

Antibodies against VP7 and VP4 are partially protective but the initial infection does not lead to permanent immunity and reinfection can occur at any age. However, subsequent infections are usually less severe than the primary infection.
 

Vaccine

Reassortant vaccines are created by genetic reassortment in which non-human rotavirus strains express the antigens of human rotaviruses on their surface. The non-human strains replicate but do not cause disease and are of low pathogenicity in humans.

A live, tetravalent rhesus-human reassortant vaccine (Rotashield - Wyeth Laboratories) was first licensed for use in infants in August 1998. It contained human G types 1, 2, 4, and simian G type 3. However, post-licensure surveillance indicated a possible relationship between the occurrence of intussusception 3 to 20 days after the vaccine was administered, especially the first dose (15 cases/1.5 million doses were reported). Use of the vaccine was suspended and it was eventually removed from the market in October 1999, when studies confirmed the link between vaccination and intussusception.

RotaTeq (Merck) is a live oral vaccine licensed in the United States in 2006. It contains five reassortants (WC3 bovine rotavirus strain with surface proteins of the G1-4 and P1A human serotypes. It does not contain preservatives or thimerosal. Three doses are given at 2, 4 and 6 months of age with the minimum age for the first dose of 6 weeks. The series should not be initiated after 12 weeks. The efficacy of the RotaTeq vaccine is high with 98% reduction in severe rotavirus gastroenteritis within the first year of vaccination and a 96% reduction in hospitalization rate. There is also a 74 and 71% reduction of rotavirus gastroenteritis within the first and second years after vaccination.

RotaTeq and Kawasaki syndrome

Rotarix (Avant Immunotherapeutics/Glaxo) is a live, attenuated, monovalent vaccine that contains the G1P[8] human rotavirus strain. It was licensed in the United States in 2008. It has been studied in South America and has a two dose schedule of administration. There is no increase in intussuseption. After two doses, there is protection through the first two years of life.  Hospitalizations are reduced by 96% and severe rotavirus gastroenteritis by 90%.  The vaccine is also effective against rotavirus gastroenteritis of any severity (79%).  Significant protection was demonstrated against severe rotavirus gastroenteritis during two rotavirus seasons caused by types G1 (96%), G2 (86%), G3 (94%), G4 (95%), and G9 (85%). These are the most commonly circulating rotavirus types in the United States.

SMALL ROUND RNA VIRAL AGENTS CAUSING GASTROENTERITIS

This group of RNA viruses morphologically is subdivided in to 2 sub-groups:

• Structured - Small round structured viruses (SRSV), Calicivirus, Astrovirus
   
• Other small viruses that are relatively structureless or featureless - W (Wollan) and Ditchling.

Figure 7. Norwalk virus from stool sample from an individual with gastroenteritis.
F.P. Williams, U.S. Environmental Protection Agency

  Figure 8.  Typical morphology of Norwalk-like viruses seen by transmission electron microscopy. The individual virions have a diameter of only 27nm. Wadsworth Center of the New York State Department of Health.

Figure 9. Bovine calcivirus © 1994 Veterinary Sciences Division - Dr Stewart McNulty at Veterinary Sciences, Queen's University, Belfast.

CALICIVIRUSES

Human caliciviruses were first described in 1976.They belong to the family caliciviridae and are non-enveloped, single stand, positive sense RNA viruses. They are 27 to 35 nm in size (figure 9). They appear round in shape with icosahedral symmetry and contain a single capsid protein. The viral surface has 32 cup-shaped depressions (‘calici’= chalice or calyx i.e. cup-like) described as the ‘Star of David’ appearance. Otherwise they are similar to Norwalk group of agents.

Classification

Caliciviruses can be divided into:

• Norwalk and "Norwalk-like" viruses (NLV)
• "Sapporo-like" viruses (SLV)
• Vesiviruses
• Lagoviruses

NLV (Noroviruses) include:

• Norwalk virus
• Hawaii virus
• Snow Mountain virus
• Montgomery County virus
• Taunton (England) virus

SLV  (Sapoviruses) include:

• Sapporo virus
• Manchester virus
• Houston/86
• London/92

Epidemiology

Noroviruses are found world-wide and cause more than 23 million cases of gastroenteritis very year in the United States. They are the cause of more than half of gastroenteritis cases in the US. From seroprevalence studies, it has been found that most people have been infected by the age of four.

There are asymptomatic infections in which the patient is infectious, has seroconverted and sheds virus. The infective dose may be very low (~10pfu) and virus may continue to be secreted during the convalescent period. Protective immunity is short-lived.

Treatment

The symptoms are treated by rehydration and the use of anti-diarrheals. Complications are rare but can be found in the immunocompromized.

Spread

Norwalk virus is spread via the feco-oral route and, perhaps, also through vomit. Outbreaks spread through fecally-contaminated food or water. Norwalk viruses can survive for several days on plastic surfaces such as counter tops and telephones and in water that is chlorinated at the usual levels (up to 10 ppm). They can survive freezing and heating to 60 degrees C. They also survive in steamed shellfish.

Stool specimens, vomit, suspected food and environmental swabs (during an outbreak) may be tested using PCR (in state laboratories). Immune electron microscopy is less used. Serology may be used for epidemiologic purposes.

Control

CDC recommends disinfection of surfaces using bleach (1 part bleach to 50 parts water). Hand sterilization is also important during an outbreak.

WEB RESOURCES

Norwalk Virus Fact Sheet
CDC

Figure 10. Astrovirus © 1994 Veterinary Sciences Division - Dr Stewart McNulty at Veterinary Sciences, Queen's University, Belfast.

  Figure 11. Astrovirus © 1994 Veterinary Sciences Division - Dr Stewart McNulty at Veterinary Sciences, Queen's University, Belfast.

Figure 12. Human astrovirus US Environmental Protection Agency 

ASTROVIRUSES

Astroviruses were described in relation to an outbreak of gastroenteritis in 1975. They are small single stranded RNA, non-enveloped virus, about 27 - 32nm in size. They are round with an unbroken surface (unlike indented surface of calicivirus) (figure 10 - 12). Their appearance in the electron microscope is a 5 or 6 pointed star within a smooth edge. They contain 3 structural proteins and their genome has been sequenced.

Astroviruses are immunologically distinct from Norwalk and other Caliciviruses - they belong to the family Astroviridae

Eight human serotypes are known and there are also animal strains.
 

Clinical Features

Infants, children, immunocompromized patients and the elderly are most often affected by astrovrius infections. The incubation period is short (1 to 4 days) and is followed by watery diarrhea, abdominal cramps, headache, nausea, low-grade fever, vomiting (the latter being Iess common).
 

Epidemiology

Astroviruses are endemic worldwide, mainly in children less than 7 years of age. Presently, the true disease burden is unclear. Transmission is person-to-person via fecal-oral route and outbreaks due to fecal contamination of sea-food or water often occur.

Diagnosis

Electron microscopy and immuno-electron microscopy are especially useful since the virus is often shed in large amounts in stool. Immunofluoresence microscopy detects all serotypes. ELIZA and PCR are also used.

WEB RESOURCES

Viral Agents of Gastroenteritis Public Health Importance and Outbreak Management 
CDC

ADENOVIRUSES

Adenoviruses were first isolated in 1953 from adenoidal tissue. The double stranded DNA viruses about 70 to 75nm in diameter. Mammalian adenoviruses belong to the genus mastadenovirus. There are six sub-genera of human adenoviruses (A to F) with 51 serotypes some of which have known oncogenic potential. In the laboratory, adenoviruses have found use in gene therapy and vaccine delivery.

Adenovirus serotypes implicated in gastroenteritis are 40 and 41 which belong to serogroup F. They cause diarrheal disease in infants and children less than 4 years of age. These ubiquitous viruses are found in the population year-round and are spread by the feco-oral route. They are not shed in the nasopharynx.

The incubation period of adenoviral gastroenteritis is 3 to 10 days and diarrhea lasts 10 to 14 days; prolonged diarrhea often seen with type 40 infections. This can also lead to intussuseption, mesenteric adenitis and appendicitis.

Isolation requires a special medium, Graham 29.

Diagnosis is made by latex agglutination and ELISA tests or by electron microscopy.

Toroviruses (figure 13) belong to the family Coronaviridae and the genus Torovirus They are pathogens for both humans and animals. They are pleiomorphic, coated, single positive strand RNA viruses. In the electron microscope they have a doughnut shape (torus). They cause watery diarrhea in infants of 2 to 12 months. They are usually diagnosed by electron microscopy.

CYTOMEGALOVIRUS

These are herpes viruses which in normal people give rise to a number of diseases, particularly infectious mononucleosis in western countries. In the immunocompromized, they lead to retinitis, hepatitis and colitis.

 

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