Natural Defenses against Viral Infections:

1. Interferons (Isaacs and Lindenmann, 1957). Interferons are antiviral proteins (a class of glycoproteins) which diffuse out from infected cells, enter into the cells in the neighbourhood and impart a defense mechanism to these cells against viral infections by inhibiting the synthesis of viral proteins. These are therefore used for therapeutic and preventive purposes in viral infections, interferons are always secreted by host cells against viral infection.

2. Body Immunity. Viruses are good antigens to induce active production of specific antibodies (by lymphocytes).

3. Immunoprophylaxis – Vaccines: Vaccines contain inactivated (attenuated) virions, which cannot cause the concerned diseases, but still act as antigens to induce antibody production by the immune system of the body.

4. Chemotherapy – Antiviral Drugs: The chemotherapeutic agents antibiotics which are used in the treatment and control of bacterial diseases are ineffective for viral diseases. However, some antiviral drugs have been prepared. These include (i) Thiosemicarbozone (for treatment and prevention of smallpox), (ii) Ribavirin or Virozole (for influenza),
(iii) Deoxyuridines, Acylovir (for herpes), (iv) Foscarnet (for hepatitis-B) etc.

2g) Viruses: Study of Bacteriophages

1. Discovery of bacteriophages is associated with Twort when he reported viral disease in bacteria. The term bacteriophages was coined by De Herelle. They are viruses, which attack bacteria. A typical bacteriophage looks like a tadpole/sperm comprising a hexagonal head of protein and a tail also a protein they show binal symmetry. Head is 1000A long and 650A in width; length of the tail is 1000A. Thus, head and tail are equal in length. Infective part of the bacteriophage in most of the cases is ds-linear DNA and it is present in hexagonal head. Joint of head and tails is neck, which is covered by collar of protein. Tail ends in end plate that develops 3 pairs of tail fibers of protein. Bacteriophages that attack E.coli are called coliphage or T-phages. They were numbered as T₁, T₂, T₃, T₄, T₅, T₆, T₇ etc by Delburck, T₂, T₄, T₆ etc are T-even phages T₁, T₃, T₅, etc or T-odd phages.
2. A bacteriophage comes into contact with the bacterial (host) cell through tail fibres. A passage is created in the host cell once the mucocomplex cell wall of bacteria is broken by lysozyme of bacteriophage. Once the passage is created, ds-linear DNA of bacteriophage is dropped inside the host cell. Empty protein coat i.e. Ghost protein remains out the host cell and disappears later on. Infective part or genetic material in ÆX174 phages is ss circular DNA and it is RNA in MS-2 & R17 phages.
3. Phage DNA dropped inside host cell may be virulent or temperate. Bacterial cell is destroyed if phage DNA is virulent, bacterial cell is not destroyed is phage DNA is temperate.
4. Destruction of bacterial cell by virulent phage DNA is called lysis. The sequence of events leading to lysis of bacterial cell are:
   • Virulent phage DNA dropped inside bacterial cell.
   • Multiplication of phage DNA inside host cell i.e. Formation of prophage. Formation of complete phages. (End of latent period or period of eclipse of phages).
   • Destruction or lysis of bacterial cell (Total time: 15-20 minutes).*
5. A bacterial cell is not destroyed if phage DNA is temperate. Temperate phage DNA is attached with host DNA; this is called lysogeny. A lysogenic bacterial cell behaves normally till temperate phage DNA is attached. Lysogeny in bacteria was first reported by Lwoff. Lwoff also coined the term l-phage for those phages in which tail terminates into single tail fibre.
   • Lysogeny may be of 3 types. They are l-phage lysogeny; P₁-phage lysogeny and mu-phage lysogeny. In l-phage lysogeny, temperate phage DNA is attached with bacterial DNA at specific place i.e. at 'gal' & 'bio' genes of bacterial DNA. In P₁-phage lysogeny, temperate phage DNA is attached with any place other than gal's genes. In mu-phage lysogeny, temperate phage DNA is never attached with bacterial DNA, remain in bacterial cytoplasm as plasmid.
   • A lysogenic bacterial cell shows different behaviour when exposed to different dosages of UV rays: