Liver and gallbladder morphology of the juvenile Nile crocodile, Crocodylus niloticus (Laurenti, 1768)

This investigation illustrates the topography, gross anatomy, histology and ultrastructure of the liver and gallbladder of the Nile crocodile in order to fill the gap that exists in the literature regarding this important crocodilian. For the topographical and macroscopical descriptions the livers and gallbladders were obtained from the carcasses of slaughtered juvenile Nile crocodiles. Perfusion and immersion fixation of tissues for histology and transmission electron microscopy were performed on juvenile Nile crocodiles donated to the university. Published descriptions of other vertebrates were inevitably relied upon for comparison due to the lack of information on these two organs of the Nile crocodile. The liver was located in its own coelomic cavity with the post-pulmonary and the post-hepatic membranes intimately associated with the cranial and caudal surfaces of the bi-lobed liver respectively. The right lobe was larger than the left lobe and they were located at the level of the third to seventh intercostal spaces with their extremities extending to the ninth intercostal space. The triangular shaped liver lobes were joined dorso-medially by a narrow isthmus consisting of liver tissue. The liver was covered by Glisson’s capsule. Central veins, sinusoids and portal tracts were distributed haphazardly with no visible lobulation. The parenchymal component occupied the largest part of the liver and was formed by anastomosing and branching cell cords consisting of two-cell-thick plates in the longitudinal sectional plane and at least five hepatocytes in the cross-sectional plane. Central bile canaliculi contained microvilli originating from apical hepatocyte surfaces and were sealed off by junctional complexes. Hemosiderin granules, bile pigments, melanin pigments, lipid droplets, cholesterol ester slits and glycogen granules were observed in addition to the normal hepatic cytoplasmic organelles. Non-parenchymal cells consisted of endothelial cells, Kupffer cells, stellate cells and pit cells localized in and around the angular sinusoids. The space of Disse existed between endothelial cells and the base of the hepatocytes which was lined by microvilli. Endothelial cells were flat cells with long fenestrated cytoplasmic extensions that lined the sinusoidal wall and contained numerous endocytotic vesicles and many lysosomes. Pleomorphic Kupffer cells were located in the sinusoidal lumen, in the space of Disse and within groups of hepatocytes. They were often situated between groups of hepatocytes, connecting two adjacent sinusoids. Large phagosomes were present in the Kupffer cells and contained a combination of melanin and hemosiderin granules as well as ceroid. Phagocytosis of apoptotic and dying cells was evident. Conspicuous groups of membrane-bound tubular organelles with a filamentous or crystalline interior were present in the Kupffer cells. Stellate cells occupied a subendothelial position in the space of Disse and contained prominent lipid droplets that indented the nuclei. A solitary cilium was infrequently found projecting into the space of Disse. Myofibroblastic cells were found in the same region as stellate cells. Pit cells with indented eccentric nuclei were found in the sinusoidal lumen and in close contact with endothelial and Kupffer cells. Numerous small electron-dense membrane-bound cytoplasmic granules were present. Occasional intercalated cells resembling lymphocytes were seen in the space of Disse and forming part of the groups of hepatocytes. Glisson’s capsule extended collagenous trabeculae into the parenchymal interior and variably sized trabeculae randomly traversed the liver tissue. Portal tracts were enmeshed by a collagenous network that contained fibroblasts, lymphocytes, plasma cells and phagocytes. Portal triads consisted of branches of the portal vein, hepatic artery and bile duct with lymphatic vessels sometimes in accompaniment. Reticular fibres were positioned around hepatocyte tubules and a basal lamina supported the hepatocytes adjacent to Glisson’s capsule. Occasional unmyelinated nerve axons were present. The isthmus contained liver tissue with similar parenchymal and a non-parenchymal components. Three anatomical zones were identified in the pouch-like gallbladder that was attached caudally to the right liver lobe in the dorso-medial region. The gallbladder wall consisted of pseudostratified columnar epithelium, a lamina propria, a muscularis externa and a serosal layer. The accumulation of apical secretory granules, apical bulging, exocytosis of mucous granules and the desquamation of the apical portions of the epithelial cells into the lumen indicated different stages of the mucus secretory cycle. CopyrightDissertation (MSc)--University of Pretoria, 2012.Anatomy and PhysiologyUnrestricte

Estudo de viabilidade econômico-financeira para implantação de software de gestão de acessos para os hotéis no Estado do Paraná

Orientador: Prof. Msc. Françoise Iatski de LimaProjeto apresentado como Trabalho de Conclusão de CursoProjeto (graduação) - Universidade Federal do Paraná, Setor de Ciências Sociais Aplicadas, Curso de Ciências EconômicasInclui referênciasResumo : Este estudo visa apresentar a viabilidade econômica e financeira da implementação de um inovador software de gestão de acessos em hotéis no Paraná. A pesquisa abrange análises de mercado, produto e técnica, além da análise econômico-financeira, com foco explícito nos custos associados, fluxo de caixa e índices de rentabilidade. O software de gestão de acessos para hotéis revoluciona a experiência do hóspede, permitindo o acesso por smartphone e agilizando processos como check-in, check-out e pedidos de serviços. Integrado às fechaduras, utiliza tecnologias avançadas para garantir autenticação eficiente. Além de melhorar a eficiência operacional, oferece análise de dados valiosos para personalizar serviços e aprimorar a satisfação do cliente. O estudo evita a apresentação detalhada das funcionalidades do software, priorizando a compreensão de sua exequibilidade no turismo paranaens

Kupffer cell structure in the juvenile Nile crocodile, Crocodylus niloticus

The morphology of Kupffer cells was examined in the liver of the juvenile Nile crocodile using light microscopy and transmission electron microscopy. Pleomorphic Kupffer cells were located in the sinusoids, in the space of Disse, in the hepatic parenchyma and often connected adjacent sinusoids. The cell surfaces were irregular due to the presence of filopodia and lamelliapodia with phagocytosis of white blood cells, red blood cells and thrombocytes being evident. The cells were in close contact with endothelial cells and pit cells in the sinusoidal lumen and with stellate cells in the space of Disse. The cytoplasm contained large phagosomes comprising a combination of ceroid pigment, melanosomes and siderosomes. The nuclei were often indented and eccentrically placed due to the presence of the phagosomes. Conspicuous clusters of membrane-bound tubular organelles with a filamentous or crystalline interior were observed in the cytoplasm. The clusters were sometimes separated into smaller groups around phagosomes. A clear zone existed between the limiting membrane and the interior of these tubular organelles with the electron-dense interior profiles being, respectively, circular, angular or divided. The tubular organelles have not previously been described in Kupffer cells and possibly represent lysosomes with specialized functions. Mitochondria, microtubules, Golgi profiles, granular and smooth endoplasmic reticulum, and a few cytoplasmic lipid droplets were also present. The presence of the tubular organelles and the occurrence of the Kupffer cells in different locations in the liver of the juvenile Nile crocodile are indicative of particularly active and mobile cells.http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4687hb201

Detection and characterisation of papillomavirus in skin lesions of giraffe and sable antelope in South Africa

Papillomavirus was detected electron microscopically in cutaneous fibropapillomas of a giraffe (Giraffa camelopardalis) and a sable antelope (Hippotragus niger). The virus particles measured 45 nm in diameter. Histopathologically, the lesions showed histopathological features similar to those of equine sarcoid as well as positive immunoperoxidase-staining of tissue sections for papillomavirus antigen. Polymerase chain reaction (PCR) detected bovine papillomavirus (BPV) DNA. Bovine papillomavirus-1 was characterised by real-time PCR in the sable and giraffe, and cloning and sequencing of the PCR product revealed a similarity to BPV-1. As in the 1st giraffe, the lesions from a 2nd giraffe revealed locally malignant pleomorphism, possibly indicating the lesional end-point of papilloma infection. Neither virus particles nor positively staining papillomavirus antigen could be demonstrated in the 2nd giraffe but papillomavirus DNA was detected by real-time PCR which corresponded with BPV-1 and BPV-2

Infestation of Mangifera indica by the mango gall fly, Procontarinia matteiana, (Kieffer & Cecconi) (Diptera: Cecidomyiidae)

Mango gall fly (Procontarinia matteiana Kieffer&Cecconi, 1906) is an orchard pest that infests flush leaves of mango, forming wart-like structures on the leaves. Serious outbreaks may result in reduced fruit yield. A natural parasite (Chrysonotomyia pulcherimma Kerrich, 1970) of the gall fly lays its eggs inside the gall and the larvae feed on the gall fly. Mango cultivars present varying susceptibilities to gall fly infestation, with cultivars ranging from completely resistant, highly susceptible to intermediate stages where pseudo-galls are formed. The latter cultivars are ovipositioned by the gall fly, but secondary metabolites within the leaves possibly halt the development, thereby preventing the development of true galls. Microscopy was used to identify characteristic features of the gall fly and its parasite inside the gall, to study the development of the insects and to distinguish them. Evidence was obtained that the use of insecticides curbs the development of the larvae. Tissue development within true and pseudo-galls was studied to provide insights into the role of secondary plant metabolites in arresting true gall formation. This study will contribute to a more holistic approach to pest management of mango.http://www.journals.co.za/ej/ejour_ento.htmlam2013ab201

Molecular detection of yaba monkey tumor virus from a vervet monkey

Yaba monkey tumour virus (YMTV) was first diagnosed in a colony of captive rhesus monkeys (Macaca mulatta) in Yaba, Nigeria. It has been implicated as the cause of cutaneous nodules in wild baboons (Papio species), rhesus monkeys (Macaca mulatta) and cynomolgus monkeys (Macaca fascicularis). This article reports a case of cutaneous pox lesions caused by YMTV in a  free-ranging  adult  female  vervet  monkey  (Chlorocebus  pygerythrus)  from  the  Umkomaas coastal area in South Africa. The virus was identified by molecular sequencing from fragments of the insulin metalloprotease-like protein and intracellular mature virion membrane protein as well as the DNA polymerase genes. Phylogenetic analyses of these gene regions revealed a 99% similarity of the sample to YMTV. Although human disease caused by YMTV is normally mild,  it  is  recommended  that  persons  in  contact  with  non-human  primates  in  the  area  of Umkomaas who develop cutaneous lesions should inform their doctors of the possibility of this infection. The extent and significance of the virus to human and non-human primates in South Africa are not known. To the authors’ knowledge, this is the first diagnosis of YMTV in South Africa and in vervet monkeys

Paraquat intoxication and associated pathological findings in three dogs in South Africa

Paraquat is a bipyridylium non-selective contact herbicide commonly used worldwide. When ingestion occurs by humans and animals either accidentally, intentionally or maliciously, paraquat selectively accumulates in the lungs resulting in the production of oxygen-free radicals, causing membrane damage and cell death. Intoxicated subjects typically show progressive and fatal pulmonary haemorrhage, collapse and oedema. In individuals surviving the acute phase, pulmonary fibrosis develops. Gastrointestinal-, renal- and central nervous system clinical signs may also occur. Owing to the lack of effective treatment and absence of an antidote, the prognosis is poor. The clinical presentation, clinicopathological findings and treatment are briefly described of three dogs from one South African household, intoxicated with paraquat. Macroscopic and microscopic lesions in one dog that was necropsied, as well as pulmonary ultrastructure are detailed and illustrated for academic reference. All dogs presented with tachypnoea and dyspnoea 2–3 days after accidental paraquat ingestion. Treatment was aimed at reducing gastrointestinal absorption, enhancing elimination by diuresis and avoiding further oxidative damage by administration of antioxidants. All dogs, however, became progressively hypoxic despite treatment and were euthanised. Paraquat toxicity should be a differential diagnosis in dogs with unexplained progressive respiratory and gastrointestinal signs and renal failure. The local veterinary profession should be aware of accidental or intentional paraquat toxicity of animals. Existing literature, variations possible in canine clinical signs, measured parameters, lesions, as well as possible treatments, promising experimental antidotes and management options are discussed.http://www.jsava.co.zaam2016Animal and Wildlife SciencesParaclinical Science

Ultrastructure of Sarcocystis bertrami sarcocysts from a naturally infected donkey (Equus asinus) from Egypt

There is considerable confusion concerning Sarcocystis species in equids. Little is known of Sarcocystis infections in donkeys (Equus asinus). Here we describe the structure of Sarcocystis bertrami-like from the donkey by light microscopy (LM) and transmission electron microscopy (TEM). Nineteen sarcocysts from the tongue of a donkey from Egypt were studied both by LM and TEM. By LM, all sarcocysts had variably shaped and sized projections on the sarcocyst walls, giving it a thin-walled to thick-walled appearance, depending on individual sarcocyst and plane of section. By TEM, sarcocysts walls had villar protrusions (vp) of type 11. The sarcocyst wall had conical to slender vp, up to 6 µm long and 1 µm wide; the vp were folded over the sarcocyst wall. The total thickness of the sarcocyst wall with ground substance layer (gs) was 1-3 µm. The vp had microtubules (mt) that originated deeper in the gs and continued up to the tip. The apical part of the vp had electron dense granules. The mt were configured into 3 types: a tuft of electron dense mt1 extending the entire length of the vp with a tuft of medium electron dense mt2 appearing in parallel, and fine mt3 present only in the villar tips. The gs was mainly smooth with few indistinct granules. All sarcocysts were mature and contained metrocytes and bradyzoites. Bradyzoites were approximately 11-15 × 2-3 µm in size with typical organelles.http://journals.cambridge.org/action/displayJournal?jid=PAR2016-07-30hb201

Pathology of fatal lineage 1 and 2 West Nile virus infections in horses in South Africa

Since 2007, West Nile virus (WNV) has been reported in South African horses, causing severe neurological signs. All cases were of lineage 2, except for one case that clustered with lineage 1 viruses. In the present study, gross and microscopic lesions of six South African lineage 2-infected horses and the one lineage 1 case are described. Diagnoses were confirmed by real-time reverse-transcriptase polymerase chain reaction (RT-PCR) of central nervous system (CNS) tissue and one by RT-PCR of a brain virus isolate. The CNS of all cases was negative by RT-PCR or immunohistochemistry (IHC) for African horse sickness (AHS), equine encephalosis virus, equine herpes viruses 1 and 4, other zoonotic flaviviruses, alphaviruses, and shunivirus, and either by immunofluorescence or IHC for rabies. Gross visceral lesions were nonspecific but often mimicked those of AHS. The CNS histopathology of WNV lineage 2 cases resembled the nonsuppurative polioencephalomyelitis reported in the Northern Hemisphere lineage 1 and recent Hungarian lineage 2 cases. Occasional meningitis, focal spinal ventral horn poliomalacia, dorsal and lateral horn poliomyelitis, leucomyelitis, asymmetrical ventral motor spinal neuritis and frequent olfactory region involvement were also seen. Lineage 2 cases displayed marked variations in CNS lesion severity, type and distribution, and suggested various viral entry routes into the CNS, based on findings in experimental mice and hamsters. Lineage 1 lesions were comparable to the milder lineage 2 cases. West Nile virus IHC on CNS sections with marked lesions from all cases elicited only two antigen-positive cells in the olfactory cortex of one case. The presence in the CNS of T-lymphocytes, B-lymphocytes, plasma cells and macrophage-monocytes was confirmed by cluster of differentiation (CD) 3, CD20, multiple myeloma oncogene 1 (MUM1) and macrophage (MAC) 387 IHC.http://www.jsava.co.zaam201