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Coprological examination of 19 Madagascan chameleons of the genera Furcifer and Brookesia revealed the presence of five new coccidian species. Isospora brygooi n. sp. from Furcifer pardalis has spherical to subspherical oöcysts with a slightly pitted wall, 20.7 (17-24.5) x 19.3 (16-23) microm and broadly ellipsoidal sporocysts, 12.2 (11.5-13) x 8.1 (8-8.5) microm, with Stieda and substieda bodies. Oöcysts of Eimeria glawi n. sp. from Furcifer pardalis are cylindrical to ellipsoidal, 27.7 (26-29.5) x 18.4 (17-19) microm, with ellipsoidal sporocysts, 7.3 (6.5-8) x 5.2 (5-5.5) microm. E. vencesi n. sp. described from F. pardalis has spherical to subspherical oöcysts, 14.3 (13-15.5) x 13.0 (12-13) microm, with small granules, one to three globular polar granules and ellipsoidal sporocysts, 7.3 (6.5-8) x 5.2 (5-5.5) microm. E. worthi n. sp., described from Furcifer oustaleti has spherical oöcysts, 17.9 (17.5-19.0) x 15.0 (14.5-16.0) microm without a polar granule and ellipsoidal to cylindroidal sporocysts, 8.2 (7.0-9.5) x 5.8 (5.0-6.5) microm. Oöcysts of E. brookesiae n. sp. from Brookesia decaryi are cylindrical, 25.6 (23-27) x 15.0 (13-16) microm with ellipsoidal sporocysts, 10.1 (9-11) x 6.9 (6-7) microm. Endogenous development of E. vencesi is confined to the intestine, while that of E. glawi occurs in the gall-bladder.

Three new species of Eimeria are described from iguanid lizards of Central and South America. The oocysts of each species have no micropyles or residua and the sporocysts lack Stieda bodies, but all have a sporocyst residuum. Eimeria sanctaluciae n.sp. was found in the St. Lucia tree lizard, Anolis luciae, collected from the Maria Islands, Lesser Antilles. The oocysts are spherical to subspherical, averaging 17.3 x 16.5 microns, with a single layered colourless wall; about 60% contain polar granules. The sporocysts are ellipsoidal and average 7.7 x 5.5 microns. Eimeria liolaemi n.sp. was recovered from the blue-gold swift, Liolaemus taenius, from Chile. The oocysts are spherical to subspherical, measuring 21 x 20.1 microns with a single-layered colourless wall. The sporocysts are subspherical and average 7.4 x 6.8 microns. Eimeria caesicia n.sp. is described from the Brazilian collared iguanid, Tropidurus torquatus. The oocysts measure 27.4 x 23.7 microns, are spherical to subspherical, with a bilayered wall, the outer surface of which appears pale blue in colour, the thin, inner wall appearing brown, when viewed by direct light under the optical microscope. The sporocysts are subspherical and average 9.4 x 7.2 microns. Unnamed polysporocystid oocysts with dizoic sporocysts are reported from the faeces of the lesser St. Vincent tree lizard, Anolis trinitatis and the possibility of spurious parasitism briefly discussed. In addition, oocysts of an unnamed Isospora sp. with a smooth oocyst wall which closely resembles I. reui were recovered from A. trinitatis.

The absorption of glycine and proline through the mid-intestines of chicks infected with Eimeria acervulina was impaired when the amino acids were presented to the mucosal surface as the dipeptide, glycylproline.

The ultrastructural development of Eimeria tenella was studied in experimentally infected chicks fed 90 ppm lasalocid, an ionophorous anticoccidial antibiotic. Drug treatment was timed to target-specific endogenous stages. At 6 h after infection, many sporozoites within the epithelium showed degradation as a result of drug action. Only a few intact sporozoites were seen. The drug caused outer-membrane blistering, large surface swellings and enlarged mitochondria in both first- and second-generation merozoites. No effect on the gamonts was discerned.

Sporozoites of Eimeria tenella were treated with lasalocid in vitro and their viability tested by inoculating them into the allantoic cavity of 11-day-old chicken embryos. Concentrations of 0.1, 1.0 and 10.0 micrograms ml-1 reduced sporozoite viability, as judged by oocyst production. Injections into the embryos of 5, 50 or 500 micrograms of lasalocid 92-93 h after infection also reduced oocyst production, indicating activity against the later stages of the life cycle.

The oral administration of whole blood and liver or lung homogenates from mice donors inoculated 1-3 days previously with Eimeria vermiformis oocysts produced infection in coccidia-free recipient mice.

Oocyst wall formation in Eimeria maxima was studied during the macrogamete stage in intestinal cells of the chick and in unsporulated oocysts isolated from faeces. The outer of the 2 membranes bounding the mature macrogamete separated from the surface but remained as a veil surrounding the developing oocyst throughout the whole intracellular process. Wall-forming bodies Type I were initially applied to the limiting membrane of the zygote cytoplasm; a layer of material similar to their contents was then formed around the zygote. As this occurred a new double membrane was formed surrounding the oocyst cytoplasm. The outer wall layer was initially homogenous in appearance but later developed into 2 zones, an outer amorphous region and an inner osmiophilic region. The inner layer of the oocyst wall was formed from the contents of the wall-forming bodies Type II which dispersed between the outer wall and the limiting membranes of the oocyst cytoplasm. There was evidence of an additional membrane formed external to the outer wall. The outer membranes were not present around the wall of oocysts passed in the faeces of chicks, but the same wall zonation was evident, although the inner osmiophilic zone of the outer wall layer was markedly thinner in comparison with the same zone seen in the tissues.

The structure and development of microgametocytes pf Eimeria maxima from chicks killed during the 6th day of infection were examined using transmission and scanning electron microscopy. Initially, nucleoli disappear and the surface of the microgametocyte invaginates. This is followed by a condensation of the chromatin which then lies at the periphery of the nuclei. Concurrent with this, the flagella are formed and they project into the parasitophorous vacuole and internal invaginations. Eventually, the nuclei become more dense and are seen to protrude from the periphery of the gametocyte. The surface view of mature microgametocytes consists of a large number of closely packed flagella.

The ultrastructure of the macrogamete and developing oocyst of Eimeria maxima (Weybridge strain) was examined in the intestinal cells of chicks fed 3 different anticoccidial drugs. Amprolium at 125 p.p.m., arprinocid at 35 p.p.m. and dinitolmide at 250 p.p.m. caused considerable morphological abnormality and incomplete development of the wall-forming bodies of Type 2 (WFB II), which did not appear able to participate in oocyst wall formation. The wall-forming bodies of Type 1 (WFB I) were able in each case to participate in oocyst wall formation although amprolium and dinitolmide produced morphological abnormalities in them. In birds medicated with dinitolmide, the outer layer of the oocyst wall was formed initially at opposite poles of the macrogametes rather than as a uniform layer. Other abnormalities resulting from drug treatment are reported and some evidence that intravacuolar tubules may be formed by the parasite pellicle is presented.

Eimeria cernae is recorded for the first time in England and the life-cycle is described in experimentally infected bank-voles (Clethrionomys glareolus). The pre-patent period was 6 days and the patent period was 4-6 days. Oocysts were ellipsoidal in shape and measured 20.2 x 15.9 micrometers. Sporocysts, measuring 11.5 micrometers long and 6.8 micrometers wide, possessed a small stieda body and contained a mass of granular sporocyst residuum. The endogenous stages developed in the epithelial cells of the colon and rectum. Three generations of schizonts were found. The 1st-generation schizont seen at 48 h post-infection (p.i.) contained up to 8 merozoites, the 2nd-generation schizont seen at 72 hr p.i. had a mean number of 16 (12-20) merozoites and the 3rd-generation schizont at 96 h p.i. had a mean of 18 (14-21) merozoites. Gamogonic stages were present from 96 to 120 h p.i. in the rectum only.

Macrogametogony and the formation of the oocyst wall has been examined in Eimeria acervulina. Macrogametes develop within a parasitophorous vacuole. Within the cytoplasm can be observed wall-forming bodies of Type I (WFBI) and Type II (WFBII), a nucleus, mitochondria, canaliculi and polysaccharide granules. WFBII are unusual in possessing a membrane internal to the granular endoplasmic reticulum. Formation of the outer layer of the oocyst wall is preceded by the separation of a veil membrane, and accompanied by morphological changes in the WFBI. WFBI material is deposited between the veil-forming membrane and the two cytoplasmic membranes. A newly formed membrane divides this outer layer during its early development. The inner layer of the oocyst wall is formed from WFBII material which is deposited between the cytoplasmic limiting membranes. The outer layer of the oocyst wall consists of granular and osmiophilic parts, but the inner layer of the wall is homogeneous.

Medication of chicks with 125 ppm amprolium or dinitolmide adversely affected oocyst sporulation of Eimeria acervulina (Weybridge strain). Dinitolmide delayed oocyst production and no oocyst wall formation was seen up to 168 h post infection. Both drugs caused large numbers of abnormally small wall-forming bodies to be produced in the macrogametes. In amprolium-fed chicks, abnormal oocyst wall formation was seen. It was concluded that the main drug action was against wall forming bodies of type 2.

The ultrastructure of microgametogenesis of Eimeria bakuensis was studied in the intestinal epithelium of an experimentally infected sheep. During development the nuclei became situated peripherally in the microgamont. Nuclear chromatin condensed into peripheral, dense portions that became the nuclei of the microgametes. The young microgamont was surrounded by a very narrow parasitophorous vacuole which widened during development and contained a few intravacuolar folds. Fissures and invaginations developed in the microgamont at the time the flagella began to grow. Polysaccharide granules were not present in the early and intermediate microgamonts but increased in number during the later stages and remained in the residual cytoplasm of the mature stage.

Medication of chicks with 70 p.p.m. arprinocid in the food, starting 2 days prior to inoculation with Eimeria tenella, resulted in decreased oocyst production and oocyst sporulation. The main morphological alteration seen during the development of the second-generation schizont was a reduction in the number of second-generation merozoites due to incomplete merogony, resulting in large masses of vacuolated residual cytoplasm. In places around the developing macrogamete the integrity of the parasitophorous vacuole was lost by either the host cell limiting membrane making contact with the parasite pellicle, or the disruption of one or both of these surfaces apparently brought about by the intervention of the host cell mitochondria. Thirty p.p.m. arprinocid reduced sporulation of the oocysts of E. brunetti and caused enlargement of the perinuclear space in the late merozoites and swelling of the endoplasmic reticulum around wall-forming bodies II.

The fine structure of the developing macrogamete of Eimeria maxima was studied from chicks killed at intervals from 138 to 147 h after inoculation. The macrogamete developed within a parasitophorous vacuole. Lying within the vacuole and extending for some distance around the periphery of the macrogamete were intravacuolar tubules, grouped in certain areas, and in some cases they were seen to make direct connexions with the cytoplasm of the parasite. During development, electron-pale vesicles were pinched off externally from the surface of the macrogamete. There appeared to be 2 forms of wall-forming bodies of the Type I during development, one form being less osmiophilic than the other. Other organelles present, such as wall-forming bodies of Type II, granular endoplasmic reticulum, mitochondria, canaliculi, lipid inclusions and intravacuolar folds, were similar in structure to those of other Eimeria species.

A new species, Eimeria mauritiensis (Apicomplexa: Eimeriidae) is reported from the pink pigeon, Nesoenas mayeri (Aves: Columbiformes) in Mauritius. Oocysts are sub-spherical 17.8 x 19.7 (16-19 x 18-22) μm: Shape index (mean length / mean width) 1.1. A micropyle, oocyst residuum and polar granules are absent. Sporocysts are 6.6 x 12.0 (6-7 x 8-14) μm with Stieda and substieda bodies. [ABSTRACT FROM AUTHOR]

The article presents information on parasite Eimeria metchnikovi Reichenow, found in the spleen of 3 of 291 gudgeon, Gohio gobio L., from Enfield Lock on the River Lee and from 2 of 10 gudgeon from the River Roding in south-east England. The primary site of this parasite appears to be the spleen but researchers also recorded oocysts in the liver, kidneys and intestines. In Hungary, researchers Pellerdy & Molnar reported E. metchnikovi mainly from the spleens of gudgeons and they considered this coccidian to be the unnamed parasite described by researchers Arvy & Moreau in the spleen and liver of gudgeon from the Dordogne.