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Repeated infection of cats with Brugia pahangi: parasitological observations

Published online by Cambridge University Press:  06 April 2009

D. A. Denham
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT
F. Medeiros
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT
C. Baldwin
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT
H. Kumar
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT
I. C. T. Midwinter
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT
D. W. Birch
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT
A. Smail
Affiliation:
The London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT

Extract

Cats were repeatedly inoculated with infective larvae of Brugia pahangi. On parasitological grounds they could be divided into 5 groups. Group I – most cats (some 70%) became microfilaraemic (mf+) and retained high levels of microfilariae (mf) in their blood for over 2 years. In some Group I cats mf counts stabilized at high levels whilst in others mf counts continued to increase. Large numbers of fecund adult worms were recovered from their lymphatics. Adult counts were not made on the cats in the current experiments but over 100 adults have been recovered from ‘super-susceptible’ cats. Large amounts of B. pahangi adult antigen were consistently present in the serum of all Group I cats. About 30% of cats became amicrofilaraemic (mf–). In these cats the peak mf levels were seldom above 10000 mf/ml. Group II – these cats had less than 10 000 mf/ml and low antigen levels. After more than 1 year of being repeatedly infected B. pahangi adult antigen slowly declined and eventually could no longer be detected in their serum and the number of mf declined very slowly after the fall in antigen levels. This shows that in Group II cats the adult worms die and as the cats are resistant to the development of the continuing weekly inoculation of L3 no new adults can develop. Group III – these cats became mf – during the first year of infection but remained B. pahangi antigen-positive for many weeks after this and, at autopsy, had living adults in their lymphatics. Group IV – in these cats there was a sudden decline in the number of mf, usually in the first year and after they have received a relatively small number of re-infections. Circulating adult B. pahangi antigen disappeared from the serum within a short time of the loss of mf and at autopsy no adult female worms were found. Group V – these cats do not become mf+ when infected. These groups are compared to the parasitological groups seen in areas endemic for infection with Wuchereria bancrofti.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

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