Experimental Infections with Mycobacterium intracellulare

1981 ◽  
Vol 3 (5) ◽  
pp. 973-978 ◽  
Author(s):  
P. R. Gangadharam ◽  
P. F. Pratt ◽  
P. T. Davidson
1963 ◽  
Vol 41 (5) ◽  
pp. 881-888 ◽  
Author(s):  
Hilda Lei Ching

Maritrema laricola sp. n. from the intestine of the glaucous-winged gull, Larus glaucescens, differs from other species in the genus in having an elongate body, small cirrus sac, and short, curved cirrus. The life cycle of the species was followed from sporocyst stage in Littorina scutulata and Littorina sitchana, to the metacercarial stage in Hemigrapsus oregonensis and H. nudus, and to the adult in natural and experimental hosts. In experimental infections of H. oregonensis, the cercariae penetrate and develop in the gills after which they migrate to the haemocoel of the crab and encyst. The metacercariae are fully developed in from 6 to 9 weeks, and similar in size and morphology to natural infections in crabs. Excystment of the metacercariae occurs in the following cultures at 40 °C: 3% pepsin plus 1% HCl, 0.85% saline, and seawater diluted 1:4. Metacercariae live for about 3 days in diluted seawater but do not produce eggs in any of the cultures. Only immature worms were recovered from mice and newly hatched chicks when they were fed the metacercariae, but mature worms were found in natural and experimental infections of the glaucous-winged gull. In a review of the genus Maritrema, the following transfers are made: Maritrema uca Sarkisian, 1957 to the genus Mecynophallus Cable, Connor, and Balling, 1960, and Maritreminoides raminellae Dery, 1958 to Pseudospelotrema Yamaguti, 1939.


Aquaculture ◽  
1996 ◽  
Vol 141 (1-2) ◽  
pp. 41-57 ◽  
Author(s):  
O.L.M. Haenen ◽  
T.A.M. van Wijngaarden ◽  
M.H.T. van der Heijden ◽  
J. Höglund ◽  
J.B.J.W. Cornelissen ◽  
...  

1946 ◽  
Vol 84 (4) ◽  
pp. 277-292 ◽  
Author(s):  
S. Edward Sulkin ◽  
Christine Zarafonetis ◽  
Andres Goth

Anesthesia with diethyl ether significantly alters the course and outcome of experimental infections with the equine encephalomyelitis virus (Eastern or Western type) or with the St. Louis encephalitis virus. No comparable effect is observed in experimental infections produced with rabies or poliomyelitis (Lansing) viruses. The neurotropic virus infections altered by ether anesthesia are those caused by viruses which are destroyed in vitro by this anesthetic, and those infections not affected by ether anesthesia are caused by viruses which apparently are not destroyed by ether in vitro. Another striking difference between these two groups of viruses is their pathogenesis in the animal host; those which are inhibited in vivo by ether anesthesia tend to infect cells of the cortex, basal ganglia, and only occasionally the cervical region of the cord. On the other hand, those which are not inhibited in vivo by ether anesthesia tend to involve cells of the lower central nervous system and in the case of rabies, peripheral nerves. This difference is of considerable importance in view of the fact that anesthetics affect cells of the lower central nervous system only in very high concentrations. It is obvious from the complexity of the problem that no clear-cut statement can be made at this point as to the mechanism of the observed effect of ether anesthesia in reducing the mortality rate in certain of the experimental neurotropic virus infections. Important possibilities include a direct specific effect of diethyl ether upon the virus and a less direct effect of the anesthetic upon the virus through its alteration of the metabolism of the host cell.


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