[
Southeast Asian J Trop Med Public Health,
1985]
Infective larvae of subperiodic B. malayi from South Kalimantan (Borneo), Indonesia collected from laboratory-raised Ae. togoi mosquitoes after feeding on infected mongolian gerbils (Meriones unguiculatus) were inoculated subcutaneously into the groin areas of 15 SD and 36 LE rats. Blood was examined weekly by membrane filtration and thick smears starting 10 weeks post-infection. Microfilariae were found in 3 SD and 4 LE rats, the mf infection rate of 20% and 11% respectively. The prepatent period was significantly shorter in the SD rats (99-112 days) than those in the LE rats (110-153 days). The patent period was longer in the LE rats (208-703 days) than in the SD rats (236-543 days), and the mf density was similar (17.5 mf/20 c.mm blood against 16 mf/20 c.mm blood). At necropsy, 6 (3 female and 3 male) adult worms were recovered from 3 of 6 SD rats and 12 (9 female and 3 male) adult worms from 4 of 20 LE rats; all worms were found in the testes. The results of xenodiagnostic, histochemical staining and measuring spicules and protuberances, demonstrated clearly the difference between both species of Brugia. All dissected Ar. subalbatus mosquitoes exposed to B. pahangi became infected (100%), but none of those to subperiodic B. malayi were infected (0%). The mf of both species of Brugia in thick films stained with naphthol-AS-TR-phosphate showed that the excretory and anal pores of subperiodic B. malayi mf exhibited acid phosphatase activity and only a little activity was seen in other parts; while B. pahangi mf showed heavy diffuse acid phosphatase activity along the entire length of the body.(ABSTRACT TRUNCATED AT 250 WORDS)
[
Mycologia,
1972]
The hyphomycete Asteromyces cruciatus F. & Mme Moreau was described without a Latin diagnosis or a designated type. The taxon was validated by Hennebert. The known distribution of this monotypic genus has been limited. F. and Mme Moreau found the fungus in sand dunes at Point du Siege (under Psamma sp.) and between Franceville and Le Home (under Agropyrum sp.) on the Normandy coast of France. Brown found A. cruciatus in open sand in the intertidal zone at Studland, Dorset and Sandwich, Kent, England; and Nicot found it in sand dunes and beach samples at Malo-les-Bains on the North Sea coast of France.
[
J Parasitol,
1953]
The axenic cultivation (i.e., growth in the absence of other living organisms) of the free-living soil nematode, Rhabditis briggsae, requires a complex medium including one or more heat-labile, protein-like substances which have been termed "factor Rb". It has been shown that factor Rb can be provided by preparations from liver or chick embryo juice or by human plasma or certain of its fractions. Moreover, it has recently been reported in abstract that a dialysed fraction of buffered aqueous liver extract will support excellent growth of R. briggsae when supplemented with known substances only. The present paper reports the results of recent studies on the nature and properties of factor Rb in liver protein and on various supplementations of certain unheated liver preparations as media for R. briggsae. Aqueous, unheated horse liver extract (hereinafter referred to as LE), prepared by centrifuging liver homogenate and taking supernatant, has been treated in various ways to provide information on the properties of factor Rb. Such preparations have been variously supplemented and tested as media for the axenic cultivation of R. briggsae. The principle supplementation used has been the supernatant (ALE) from autoclaved LE. Both partly and completely defined supplementations have also been employed. From these studies some advance has been made in the direction of a completely defined medium for R.