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LIVE POLIO IRUS VACCINES

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62<br />

Safety-Laboratory Evidence of Attenuation and Safety<br />

__<br />

Log. 1 0<br />

PFU/ml.<br />

-8 , _<br />

40 ° C.<br />

37 ° C.<br />

MAH<br />

-6 'L<br />

-4 '<br />

-- ?_ C- L¿<br />

2 6 10 Hrs.<br />

FIG. 2<br />

TABLE 13. COMPARATIVE INFECTIVITY OF INTACT V<strong>IRUS</strong> AND INFECTIOUS RIBONUCLEIC ACID FOR<br />

THE MS AND MK CELLS<br />

V<strong>IRUS</strong> INOCULUM RATIO OF TCD50 OF MS TO MK<br />

CHAT INTACT V<strong>IRUS</strong> 1 : 6<br />

RNA 3.3: 1<br />

MAHONEY INTACT V<strong>IRUS</strong> 3 : 1<br />

RNA 3.7 : 1<br />

the system used by Holland, where infectious<br />

nucleic acid will yield intact virus non-infectious<br />

for the cell system into which it was introduced.<br />

Similar results were obtained when intact CHAT<br />

virus was used to infect MS cells in the presence<br />

of deuterium oxide (heavy water) in the medium.<br />

Substitution of hydrogen by deuterium in<br />

]iving systems has been studied for some time in<br />

various laboratories and has been found to have<br />

distinetive biologic effects. In the field of virus<br />

infections, the burst size of T7 bacteriophage<br />

was increased when the phase was permitted to<br />

multiply in E. coli grown in D 2 0 medium instead<br />

of H 2 0 medium. The data presented in<br />

Table 14 seem to indicate that the plating efficiency<br />

of CHAT virus on MS cells grown in

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