EXPERIMENTAL STUDIES ON STRONGYLOIDES AGOUTII IN THE GUINEA PIG

1940 ◽  
Vol 18d (9) ◽  
pp. 307-324 ◽  
Author(s):  
Henry J. Griffiths

The suitability and tolerance of the guinea pig to infection with Strongyloides agoutii presented an opportunity for the study of the bionomics of this species in an experimental host.Serial transfer of this nematode through the guinea pig yielded a mixed type (free males and filariform larvae) of free-living development in faecal cultures which occasionally reverted to the indirect mode common to S. agoutii. A reversion to the indirect mode of development was produced when ova from faeces of guinea pigs infected with S. agoutii were cultured in sterile agouti faeces.The termination of the prepatent period of S. agoutii in the guinea pig was shown to range from 7 to 10 days, and 71% of 58 animals were positive by faecal test by the eighth day. The patent period ranged from three to eight weeks.The guinea pig was shown to develop an absolute acquired immunity to re-infection with S. agoutii. This resistance has been retained over a period of at least 6 to 13 months. An age resistance was not observed in animals one year old and over.

1920 ◽  
Vol 32 (5) ◽  
pp. 601-625 ◽  
Author(s):  
Hideyo Noguchi ◽  
I. J. Kligler

Injections into guinea pigs of the blood and the emulsions of liver and kidney obtained at autopsy from a fatal case of yellow fever in Merida induced in some of these animals, after a period of several days incubation, a rise of temperature which lasted 1, 2, or more days. When killed for examination at this febrile stage the animals invariably showed hemorrhagic areas of various size, sometimes few and sometimes numerous, in the lungs, and also, though less constantly, in the gastrointestinal mucosa, together with general hyperemia of the liver and kidneys. In a guinea pig (No. 6) inoculated with the liver emulsion of Case 1 there was a trace of jaundice on the 9th day. Injections of the blood or liver and kidney emulsions from such animals into normal guinea pigs reproduced the febrile reactions and the visceral lesions. The majority of the animals which were allowed to live and complete the course of the infection rapidly returned to normal (within several days). Examinations of these surviving guinea pigs after 2 weeks revealed the presence of rather old hemorrhagic foci in the lungs. In the course of further attempts to transfer the passage strain, a secondary infection by a bacillus of the paratyphoid group caused many deaths among the guinea pigs and resulted finally in the loss of the strain from Case 1. Most of the cultures made with the heart's blood taken at autopsy from Case 1 proved to be contaminated with a bacillus of the coli group. The contents of the apparently uncontaminated tubes were inoculated into guinea pigs, but the results were for the most part negative or vitiated by a secondary infection. Dark-field search for the leptospira with the autopsy materials was negative, although prolonged and thorough examination was not practicable at the time of these experiments. Our efforts were concentrated on obtaining positive animal transmission rather than on the time-consuming demonstration of the leptospira, which when unsuccessful does not necessarily exclude the presence of the organism in small numbers. Likewise, the dark-field work with the material from guinea pigs was confined to a brief examination and was omitted in many instances. Under these circumstances no leptospira was encountered in any of the material from Case 1. On the other hand, the results obtained with the specimens of blood from Case 2 were definitely positive, not only in the transmission of the disease directly, or indirectly by means of cultures, into guinea pigs, but also in the demonstration of the leptospira in the primary cultures and in the blood and organ emulsions of guinea pigs experimentally infected with such cultures. Definite positive direct transmissions were obtained with the specimens of blood drawn on the 2nd and 3rd days. No blood was taken on the 4th or 6th days. There were indications of abortive or mild leptospira infection in the guinea pigs inoculated with the blood taken on the 5th day. Regarding the inoculation of cultures from Case 2, it may be stated that only the cultures (leptospira +) made with the blood drawn on the 2nd day caused a definite fatal infection in guinea pigs. From this series a continuous passage in the guinea pig has been successfully accomplished. One of the guinea pigs (No. 48) inoculated with the culture 5 days old (leptospira +) made from the blood taken on the 3rd day presented typical symptoms, and a positive transfer from this to another animal (No. 98) was also made. Cultures of the blood drawn on the 5th and 7th days gave unsatisfactory results, owing to a secondary contamination. Leptospiras were detected in some of the culture tubes containing 2nd and 3rd day specimens of blood from Case 2; they were few in number and for the most part immotile, owing perhaps to some unfavorable cultural condition such as a fungus contamination. Charts 17, 18, and 19 give a summary of the experiments. See PDF for Structure


1980 ◽  
Vol 08 (03) ◽  
pp. 290-296 ◽  
Author(s):  
Yann-Ching Hwang

Guinea pig acupuncture points located on the back of the animal, cranial and caudal to the last rib in the muscular groove between longissimus dorsi and iliocostalis, were treated by electro-acupuncture (EA). In the duodenum, when compared with the control, the EA-treated group showed a significant decrease of its enterochromaffin (EC) cell count. However, the sham-treated group also had a lower EC cell count compared to the control. Decreased EC counts were also observed in the jejunum and colon in both EA and sham treated groups: however, they were not significant except in the sham-treated colon. The present study demonstrated that in the normal guinea pigs electro-acupuncture on certain points tends to cause a decrease of the EC cell count in some parts of the gut; however, such results cannot be completely attributed to the effect of acupuncture.


2002 ◽  
Vol 76 (3) ◽  
pp. 189-192 ◽  
Author(s):  
F. Audebert ◽  
H. Hoste ◽  
M.C. Durette-Desset

AbstractThe chronology of the life cycle ofTrichostrongylus retortaeformis(Zeder, 1800) (Nematoda, Trichostrongyloidea) is studied in its natural hostOryctolagus cuniculus. The free living period lasted 5 days at 24°C. Worm-free rabbits were each infectedper oswithT. retortaeformislarvae. Rabbits were killed at 12 h post-infection (p.i.) and every day from one day to 13 days p.i. By 12 h p.i., all the larvae were exsheathed and in the small intestine. The third moult occurred between 3 and 5 days p.i. and the last moult between 4 and 7 days p.i. The prepatent period lasted 12 to 13 days. The patent period lasted five and a half months. The four known life cycles of species ofTrichostrongylusin ruminants were compared with that ofT. retortaeformis. No significant difference was found except in the duration of the prepatent period. These similarities in the life cycles confirm the previously formulated hypotheses on the relationship between the parasites of the two host groups ().


1921 ◽  
Vol 34 (6) ◽  
pp. 525-535
Author(s):  
Peter K. Olitsky

The work reported in this paper relates to the bacteria which can be cultivated from the blood and spleen of guinea pigs at different stages of infection with the virus of typhus fever. The studies show that during the period of incubation and before the onset of fever no ordinary bacteria appear in the cultures, while on the 1st day of the febrile reaction different bacteria were found in 6 of 26 guinea pigs cultured; on the 2nd day, in 10 of 16; on the 3rd day, in 3 of 4; and on the 4th day in cultures of all of the 4 guinea pigs observed. The findings indicate that the virus of typhus fever is distinct from ordinary cultivable bacteria, and, as the disease set up by the virus progresses, the infected guinea pigs become subject to invasion by secondary or concurrent bacteria which thus induce a mixed infection. The bacteria which under the influence of the virus of typhus fever thus invade the body of the guinea pig are of several kinds, and vary not only among themselves, but also with the day of the fever on which the examination is made. Thus, on the 1st day of the fever Plotz' bacilli were recovered twice and anaerobic streptococci, proteus bacilli, aerobic diphtheroids, Gärtner type bacilli, and Staphylococcus aureus each once. On the 2nd day Plotz' bacilli were found four times, anaerobic streptococci three times, Gärtner type bacilli, aerobic diphtheroids, Bacillus welchii, aerobic Gram-positive diplobacilli, and Staphylococcus aureus each once. On the 3rd day Plotz' bacilli were recovered once, as were anaerobic streptococci and Grtner type bacilli. On the 4th day Staphylococcus aureus was found twice and Plotz' bacilli and Bacillus proteus each once. This variation in the kind of bacteria as well as the lack of predominance of one kind over another during the different stages of the febrile reaction in guinea pigs leads us to infer that they occur concurrently with the typhus virus. And since the more unusual of these organisms, the Plotz bacillus, the anaerobic streptococcus, the aerobic diphtheroid, and the diplobacillus are non-pathogenic for guinea pigs, while the more common bacteria such as the Gärtner type bacillus, Welch's bacillus, the proteus bacillus, and the staphylococci induce distinctive effects, and since all the bacteria could be suppressed without their reappearance in guinea pig passages of the virus containing them, we believe that they are independent and unrelated to the true virus of typhus fever.


1924 ◽  
Vol 39 (4) ◽  
pp. 589-602 ◽  
Author(s):  
H. Mooser

1. Two cases of rat-bite fever with a typical fever course and a maculopapular exanthem came under my observation in Mexico. 2. A spiral organism morphologically identical with one known in Japan as the causative agent of Sodoku was found in a Mus decumanus caught in Mexico City. 3. The organism was found to be pathogenic for white rats and guinea pigs, the infection being fatal for guinea pigs. 4. The bite of an infected guinea pig led in one of two instances to infection and death of the animal bitten. 5. The microscopical findings in the guinea pigs infected with this microorganism closely resemble in many respects the findings in Blake's case and in Kaneko and Okuda's first case, the only ones of human rat-bite fever which have been closely studied at post mortem. 6. Eye lesions were found in all the infected guinea pigs and the spiral organisms were demonstrated in the discharge from the eyes and also within the cornea. 7. Similar eye lesions were found in most of the infected rats and the secretion from the eyes of one of them was demonstrated to be infectious for guinea pigs. 8. The eye lesions constitute an evident source for the spiral organisms transmitted by biting, and not improbably the only one. My experiments may give an explanation for the transmission of some other spirochetal diseases besides rat-bite fever. Cases of Weil's diseases are reported to be caused by the bite of a rat and it is noteworthy that eye lesions occur in spirochætosis icterohæmorrhagica (Manson).


1964 ◽  
Vol 62 (2) ◽  
pp. 179-184 ◽  
Author(s):  
Alexander L. Terzin

Complement-fixation tests with psittacosis-trachoma group antigens, if set up with complement prepared from guinea-pigs cross-infected with any of the Bedsonia agents, may give completely false positive results. The use of C.F. positive or C.F. inhibition positive samples of guinea-pig sera as a source of complement can induce also a significant increase or decrease, respectively, of the actual C.F. titres in Bedsonia-positive serum samples tested. Observations made both in routine serology and in experimental studies show the necessity of testing carefully, for possible presence of Bedsonia titres, individual sera of guinea-pigs intended for use as source of complement in C.F. tests performed with Bedsonia group antigens.I have pleasure in thanking Dr F. B. Gordon and Dr E. Weiss for the valuable suggestions made and HM3 C.O. Wiese for the technical assistance.


1992 ◽  
Vol 101 (8) ◽  
pp. 699-704 ◽  
Author(s):  
Nebil Goksu ◽  
Nalan Karademir ◽  
Rifki Haziroglu ◽  
Ismet Bayramoglu ◽  
Yusuf Kemaloglu ◽  
...  

The middle ear of guinea pigs has long been used for experimental studies, but no detailed information about its temporal bone anatomy is available. In 18 adult guinea pigs, the temporal bone, eustachian tube, and inner ear anatomy, in addition to the anatomy of the middle ear, were investigated under the dissection microscope. In addition to properties of the eardrum, ossicles, air cell system, and cochlea previously described, the appearance of Huschke's foramen and the crista stapedis in an adult guinea pig ear, the structure of the eustachian tube, the architecture of the internal auditory canal, and the communication of the mastoid cells with the tympanic bulla are described. Differences and similarities among guinea pigs, other experimental animals, and humans are discussed to show the advantages and disadvantages of the guinea pig ear for experimentation.


Author(s):  
Corazon D. Bucana

In the circulating blood of man and guinea pigs, glycogen occurs primarily in polymorphonuclear neutrophils and platelets. The amount of glycogen in neutrophils increases with time after the cells leave the bone marrow, and the distribution of glycogen in neutrophils changes from an apparently random distribution to large clumps when these cells move out of the circulation to the site of inflammation in the peritoneal cavity. The objective of this study was to further investigate changes in glycogen content and distribution in neutrophils. I chose an intradermal site because it allows study of neutrophils at various stages of extravasation.Initially, osmium ferrocyanide and osmium ferricyanide were used to fix glycogen in the neutrophils for ultrastructural studies. My findings confirmed previous reports that showed that glycogen is well preserved by both these fixatives and that osmium ferricyanide protects glycogen from solubilization by uranyl acetate.I found that osmium ferrocyanide similarly protected glycogen. My studies showed, however, that the electron density of mitochondria and other cytoplasmic organelles was lower in samples fixed with osmium ferrocyanide than in samples fixed with osmium ferricyanide.


1976 ◽  
Vol 36 (02) ◽  
pp. 401-410 ◽  
Author(s):  
Buichi Fujttani ◽  
Toshimichi Tsuboi ◽  
Kazuko Takeno ◽  
Kouichi Yoshida ◽  
Masanao Shimizu

SummaryThe differences among human, rabbit and guinea-pig platelet adhesiveness as for inhibitions by adenosine, dipyridamole, chlorpromazine and acetylsalicylic acid are described, and the influence of measurement conditions on platelet adhesiveness is also reported. Platelet adhesiveness of human and animal species decreased with an increase of heparin concentrations and an increase of flow rate of blood passing through a glass bead column. Human and rabbit platelet adhesiveness was inhibited in vitro by adenosine, dipyridamole and chlorpromazine, but not by acetylsalicylic acid. On the other hand, guinea-pig platelet adhesiveness was inhibited by the four drugs including acetylsalicylic acid. In in vivo study, adenosine, dipyridamole and chlorpromazine inhibited platelet adhesiveness in rabbits and guinea-pigs. Acetylsalicylic acid showed the inhibitory effect in guinea-pigs, but not in rabbits.


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