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AGf~ICULTURAL RESEARCH, PUSA.

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266 PRACTICAL BACTERIOLOGY<br />

diameter), delicate, semi-transparent, dewdrop-like<br />

colonies, which tend to remain discrete-i.e. like<br />

colonies of streptococci.<br />

In bouillon--growth shows at first a uniform turbidity,<br />

but later forms a granular deposit in the tube.<br />

On hlood-agar-it is non-haemolytie, or only<br />

partially lytlc, and the colonies procluce the same<br />

greenish coloration as the" viridans " type of streptococcus.<br />

'I'he colony is flat and smooth, and thc cdge<br />

is often distinctly raised.<br />

Cultures may show transformation of the colonies from the<br />

typical stll()oth (t:i) type to the rmtgh (It) form; thifi variation<br />

is nsso('iated with loss 01' ('apsu[c formation, absence of typespecificity<br />

(vide infrll) and loss of virulence.<br />

Bioche;wical Reactions.-Ferl1lents various Cal'hohydrates<br />

(e.g. glucose, lactose, saccharose) and differs<br />

from most strains of streptococci in its fermentation<br />

of inulin. Hiss's scrum water, containing 1 pcr cent. of<br />

peptone, is a convenient medium for these tests. The<br />

medium used for testing the biochemical reactions of<br />

the streptococcus also gives good results (vide p. 252).<br />

It is sharply differentiated from the streptococci by its<br />

solubility in bile. This test c:omists in ac1dillg 1 part<br />

of sterile ox bile or 1 part of a sterilised 10 per cent.<br />

solution of sodium taurocholate in normal saline to<br />

10 parts of a bouillon culture. The test may also be<br />

carried out by using a 10 per cent. solution of sodium<br />

desoxycholate made distinctly alkaline to phenolphthalein,<br />

0'1. e.c. being addcd to 1 c.C. of a broth<br />

culture. This method gives very satisfactory results,<br />

lysis occurring within fifteen minutes.<br />

ViuVllity.-'l'he thermal death-point is al)out 52° C. The<br />

ordinary laboratory cultures lose viability rapidly and require<br />

to he subcultured nt short intervals (e.g. about fUUl·tecn days).<br />

Cultures survive best in a semi-solid agar containing blood.<br />

'l'he vitality and virulence of a strain can be maintained by<br />

the method described below.<br />

Expcl'itnental Inoculation. - Pathological material<br />

containing pneumococci (e.g. pneulllonic sputum) or a

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