Isospora arctopitheci Rodhain,
1933.
Synonym: Isospora scorzai
Arcay-de-Peraza, 1967.
Type host: Callithrix penicillata (I.
Geoffroy, 1812) (syn. Hapale penicillatus), Short-tusked marmoset.
Other hosts: Other natural hosts, according to
Hendricks (1974), are the marmoset, Saguinus geoffroyi (Pucheran, 1845), and
capuchin monkey, Cebus capucinus
(Linnaeus, 1758). Hendricks (1977), experimentally infected the night monkey,
Aotus
trivirgatus (Humboldt, 1811), spider monkey, Ateles fuscipes Gray, 1866,
howler
monkey, Alouatta pigra Lawrence, 1933 (syn. A. villosa), and the
squirrel monkey,
Saimiri sciureus (Linnaeus, 1758). Hendricks (1977) also reported that the
domestic
dog, Canis familiaris, coatimundi, Nasua nasua, kinkajou, Potos
flavus, tayra, Eiria
barbara, domestic cat, Felis catus (sic) and opossum, Didelphis
marsupialis could
serve as definitive hosts and transport hosts include the laboratory mouse, Mus
musculus, and chicken, Gallus gallus. Poelma (1966) reported some
isosporan oocysts
"resembling I. arctopitheci" in the African bush-baby, Galago
sengalensis, which
died the day after its arrival in the Amsterdam Zoo. Arcay-de-Peraza (1967) found
oocysts of what is likely I. arctopitheci in the feces of a Uakair monkey,
Cacajao rubicundus, that was in captivity in the London Zoo. She was able to
successfully infect Cebus nigrivittatus from Venezuela with these oocysts.
Type locality: Unknown (see Remarks).
Geographic distribution: EUROPE: Belgium (?),
England (?), Holland (?);
SOUTH AMERICA: Panama, vicinity of La Chorrera and the Canal Zone, near Cardenas
Village; Venezuela (?); AFRICA (?).


Description of oocyst: Oocyst shape: subspheroid to
ellipsoid; number of
walls: 2; wall thickness: 1; wall characteristics: outer, colorless, smooth; inner,
light yellow-brown; L x W: 27.7 x 24.3 (23-33 x 20.5-27); L/W ratio: 1.1 (1.05-1.3);
M: absent; OR: absent; PG: absent. Distinctive features of oocyst: oocyst wall is
easily deformed in handling.
Description of sporocysts and sporozoites:
Sporocyst shape: ellipsoid; L x
W: 17.6 x 12.5 (13-20.5 x 10-16); L/W ratio: 1.4 (1.2-1.6); SB: absent; SSB: absent;
PSB: absent; SR: present; SR characteristics: composed of spherical, coarse granules
in middle of sporocyst; SR L x W: 10.2 x 6.9; SP: with 1 large RB at narrow end.
Distinctive features of the sporocyst: the voluminous SR.
Prevalence: 1/1 in the type host; from
50-100% in
other naturally-infected
hosts (Arcay- de-Peraza, 1967; Hendricks, 1974; Poelma, 1966).
Sporulation: Exogenous. Oocysts sporulated in 2
days in 1% chromic acid at
RT in Belgium; 4 days in 2.5% aqueous potassium dichromate solution at 24ºC in
Panama.
Prepatent period: Varies from 5-9 days in
experimentally-infected primates (Hendricks, 1977).
Patent period: Varies from 3-55 days in
experimentally-infected primates (Hendricks, 1977).
Site of infection: Presumably small intestine.
Oocysts found in the
posterior small intestine, but no endogenous stages were found in tissue sections.
Material deposited: Photoneotype in the USNPC, No.
87407.
Cross-transmission studies: Rodhain (1933) was
unable to infect 6 young
white rats or a cynocephalus monkey (presumably [?] the yellow baboon, Papio
hamadryas [Linnaeus, 1758] [syn. P. cynocephalus]) with this species from
C.
penicillata. Hendricks (1974), however, was able to transmit this species from
Cebus
capucinus to 2 male S. geoffroyi, a juvenile and an adult. He also was able
to
transmit it to, and achieve patent infections in, 6 genera of New World primates, 5
genera of carnivores and 1 marsupial (Hendricks, 1977).
Remarks: The oocysts first seen and described by
Rodhain (1933) were from a
marmoset held in captivity at the Prince Leopold Institute in Antwerp, Belgium; the
natural origin of this host is unknown. The description here is based on Rodhain
(1933) and Hendricks (1974). Hendricks (1974) stated that the shape of sporulated
oocysts was subspheroid to ellipsoid and that the SR was "equatorial" in location;
however, his photomicrographs show oocysts which are clearly ovoid in shape
(slightly pointed at 1 end) and sporocysts that have their SR located at 1 end,
similar to that seen in I. endocallimici. Arcay-de-Peraza (1967), in a review
and comparison of the Isospora spp. found in primates, described I.
scorzai as a new
species. However, we agree with the convincing argument of Hendricks (1974) that
I. scorzai is a junior synonym of I. arctopitheci.
References: Arcay-de-Peraza (1967); Hendricks
(1974, 1977); Poelma (1966); Rodhain (1933).