Individual and combined effects of multiple pathogens on Pacific treefrogs.

In nature, individual hosts often encounter multiple pathogens simultaneously, which can lead to additive, antagonistic, or synergistic effects on hosts. Synergistic effects on infection prevalence or severity could greatly affect host populations. However, ecologists and managers often overlook the influence of pathogen combinations on hosts. This is especially true in amphibian conservation, even though multiple pathogens coexist within amphibian populations, and several pathogens have been implicated in amphibian population declines and extinctions. Using an amphibian host, Pseudacris regilla (Pacific treefrog), we experimentally investigated interactive effects among three pathogens: the trematode Ribeiroia sp. (hereafter, Ribeiroia), the fungus Batrachochytrium dendrobatidis (hereafter, BD), and the water mold Achlya flagellata. We detected no effects of A. flagellata, but did find effects of Ribeiroia and BD that varied depending on context. Low doses of Ribeiroia caused relatively few malformations, while higher Ribeiroia doses caused numerous deformities dominated by missing and reduced limbs and limb elements. Exposure to low doses of BD accelerated larval host development, despite there being no detectable BD infections, while exposure to higher BD doses caused infection but did not alter developmental rate. Hosts exposed to both Ribeiroia and BD exhibited the highest mortality, although overall evidence of interactive effects of multiple pathogens was limited. We suggest further research on the influence of multi-pathogen assemblages on amphibians, particularly under a variety of ecological conditions and with a wider diversity of hosts and pathogens.

Anomalías morfológicas y estructurales en fetos de ratones con infección aguda experimental por Trypanosoma cruzi / Morphological and structural anomalies in fetuses of mice with acute experimental infection by Trypanosoma cruzi

El presente estudio muestra el desarrollo de fetos de ratones hembras NMRI inoculadas con la cepa M/HOM/BRA/53/Y de trypanosoma cruzi y preñadas durante la fase aguda de la infección. Altos niveles de parasitemias fueron observados en las ratones con 30 días post-infección y 20 días de gestación, en comparación con las detectadas en los ratones vírgenes e infectadas con T. cruzi. En 3 de los fetos (15%) provenientes de dos madres infectadas/gestantes con altas parasitemias, se observaron signos de anomalías congénitas morfológicas y estructurales músculo-esqueléticas. Presentándose en uno de los fetos la formación de dos protuberancias, una sobre el lado dorsal del cuerpo y la otra en la base de la pata inferior izquierda, en otro de los fetos, la pata derecha se desarrolló sobre el lado derecho de la cara y en un tercer feto se formó una protuberancia en la pata anterior izquierda a nivel de la región subescapular. El estudio histopatológico con hematoxilina y eosina de los tejidos muscular esquelético y cardíaco, mostró en el 10% (2/20) de los tejidos fetales, intenso infiltrado celular mononuclear con predominio de linfocitos, macrófagos o histiocitos y monocitos entre las fibras musculares y cardíacas, con discreta miositis y miocarditis. Con la técnica de peroxidada anti peroxidada se observaron abundantes depósitos antigénicos, tanto en placenta como en músculo esquelético de los fetos con alteraciones morfológicas. En los ratones infectadas/gestantes los fetos presentaron reducción del peso corporal y retardo en el crecimiento fetal, así como reducción en el número de fetos de 10 en comparación con 14 fetos de mayor tamaño y aspecto normal desarrollados en las ratonas sanas preñadas.

The present study shows the development of the fetuses from pregnant female mice NMRI inoculated with M/HOM/BRA/53/Y Trypanosoma cruzi strain. The infection revealed the highest levels of patent parasitemia in mice with 30 days postinfection and 20 days of pregnancy in comparison with infected unmated mice. Three fetuses (15%) from two infected mice with high levels of parasitemia, showed morphological and structural muscularskeletal congenital anomalies. Two protuberances were observed, one on the dorsal side of the body, and the other on the left footpad base. In another fetus his right footpad came out from the right part of his face and in the 3rd one it was observed a lump in the left leg, above the level subscapular region. The histophatological study with hematoxilin-eosin staining of skeletal muscle and cardiac tissue, showed in 10% (2/20) of the mice, inflammatory infiltrate with lymphocytes, macrophages and monocytes into muscular and cardiac fibers, with discrete myositis and myocarditis. Peroxidase anti-peroxidase staining showed T. cruzi antigens in placenta and skeletal muscle of the fetuses with morphological alterations. In the pregnant mice, fetuses also showed both, loss of weight and growth retardation, as well as reduction of the number of fetuses to 10 in comparison with 14 fetuses in normal and healthy pregnant mice.

Malaric placentas. A quantitative study and clinico-pathological correlations.

A histological and morphometric study was conducted on 372 placentae out of a total 440 delivered in Zanzibar. Fibrin (F), intervillous space (IVS) and Villi (V) relative volumes were determined by the point-counting system and the ratio of syncytium to blood capillaries by the linear intercept method. Parasitemia load and inflammatory reaction were graded semiquantitatively by the use of a 1 mm square grid. Parasitised red cells identified active malaria (AM), the presence of malarial pigment only identified past malaria (PM), and the absence of both characterized non-malarial placentae (NM). AM(17.87%), PM(21.61%) and NM(60.52%) placentae did not vary significantly in weight. Newborns from AM had a significantly lower weight than those from PM and NM. Peripheral and placental parasitemia were not coincident. Placental parasitemia load increased parallel with birthweight. The latter decreased with the increasing severity of the inflammation, particularly with the prevalence of lymphocytes in the IVS. Significantly increased volume of F was found in AM and PM placentae, while no significant variation was noticed in IVS and V volumes. The syncytium/capillaries ratio was significantly increased in AM. We conclude that low birthweight in malaria is linked to IVS inflammation but not to F deposits or parasitemia load. Non-leukotactic lymphokines might play some role. Morphologic aspects bespeak for a less mature placenta than expected and this might represent an adaptive change.