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SYNOPSIS. A nonpathogenic histomonad, morphologically identical to that found in pheasants by Wenrich in 1943, is described as Histomonas wenrichi n. sp. Its dimensions are about 1.5 × those of H. meleagridis. It has 4 flagella instead of the 1 or 2 that characterize the latter species. It does not multiply in the host tissues nor produce visible responses to its presence there, and it does not exist as the clear “tissue form” that is common in active H. meleagridis infections. Histomonas wenrichi n. sp. can be transmitted to turkeys, chickens, and pheasants by either rectal inoculation or by feeding embryonated eggs of Heterakis gallinarum grown in birds harboring the nonpathogenic histomonad in the ceca. Usually fewer than half the female heterakids so grown produce eggs capable of transmitting this histomonad, and a total of 200 to several thousand eggs from worms recovered from Histomonas‐infected birds may be required to produce one Histomonas infection. Histomonas wenrichi n. sp. has been propagated in more than 2000 chickens and turkeys over an 8‐year period, during which time it has been transmitted by 18 generations of Heterakis. It has frequently been grown in birds in which H. meleagridis was also present, and upon reisolation it maintained all of its original characteristics. It has not yet been cultivated in vitro.

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SYNOPSIS. During a 7‐year period Histomonas meleagridis survived 1000 passages in Medium 199 fortified with serum and antibiotic‐killed bacteria. The histomonads were originally isolated from a chicken's cecal dropping, and the bacteria were cultivated from the cecal contents of a normal turkey. In many respects, the histomonads remained unchanged during cultivation, but in some other respects they changed considerably, perhaps irreversibly. Morphologically, the histomonads propagated in vitro showed only slight changes. When returned to birds, they resumed the structure characteristic of lumen‐dwelling individuals of this species. However, they had long since lost their ability to produce disease in either chickens or turkeys, and organisms of the tissue‐dwelling type were rarely seen. The long‐cultivated histomonads are actually as nonpathogenic as Histomonas wenrichi, but they have none of the distinguishing morphologic characteristics of the latter. As has been reported elsewhere, H. meleagridis long maintained in the tissue culture medium has also lost much of its ability to immunize either chickens or turkeys against infection with virulent strains of this parasite. Also lost in the process of adaptation to its restricted medium has been the ability to multiply satisfactorily in vitro with the complement of bacteria normal to the ceca of the birds. However, in some instances, histomonads which have become adapted to in vitro cultivation are still able to live in birds with this diversified flora. Activity of the histomonads cultivated in vitro differed but little from that of H. meleagridis freshly isolated from birds, when both were viewed under the same conditions. Histomonads from each of the above sources multiplied most satisfactorily in their accustomed habitat, probably because of a difference in nutritional requirements.