scholarly journals Multisystemic Abscesses in African Green Monkeys (Chlorocebus aethiops) with InvasiveKlebsiella pneumoniae—Identification of the Hypermucoviscosity Phenotype

2008 ◽  
Vol 45 (2) ◽  
pp. 226-231 ◽  
Author(s):  
N. A. Twenhafel ◽  
C. A. Whitehouse ◽  
E. L. Stevens ◽  
H. E. Hottel ◽  
C. D. Foster ◽  
...  
2019 ◽  
Vol 56 (5) ◽  
pp. 794-798
Author(s):  
Anne A. M. J. Becker ◽  
Sreekumari Rajeev ◽  
Mark A. Freeman ◽  
Amy Beierschmitt ◽  
Victoria Savinon ◽  
...  

We identified multiple extraintestinal cystacanths during routine postmortem examination of 3 small Indian mongooses and 2 African green monkeys from the Caribbean island of St. Kitts. In mongooses, cystacanths were encysted or free in the subcutaneous tissue, skeletal muscle, or peritoneal or pericardial cavities, whereas in the monkeys, they were in the cavity and parietal layer of the, tunica vaginalis, skeletal muscle, and peritoneal cavity. Morphological, histological, and molecular characterization identified these cystacanths as Oncicola venezuelensis (Acanthocephala: Oligacanthorhynchidae). There was minimal to mild lymphoplasmacytic inflammation associated with the parasite in the mongooses and moderate inflammation, mineralization, hemorrhage, and fibrosis in the connective tissue between the testis and epididymis in 1 monkey. We identified a mature male O. venezuelensis attached in the aboral jejunum of a feral cat, confirming it as the definitive host. Termites serve as intermediate hosts and lizards as paratenic hosts. This report emphasizes the role of the small Indian mongoose and African green monkey as paratenic hosts for O. venezuelensis.


2021 ◽  
Vol 7 (1) ◽  
pp. 65-69
Author(s):  
Kacou Martial N'da ◽  
Laibané Dieudonné Dahourou ◽  
Oubri Bassa Gbati ◽  
Rianatou Bada Alambedji

Background and Aim: Parasitic and infectious diseases are ubiquitous threats to primate and human populations. This study was carried out to study the diversity and frequency of gastrointestinal parasites with zoonotic potential in green monkeys in the Bandia Reserve located in Senegal. Materials and Methods: For this study, 164 stool samples of Chlorocebus aethiops sabaeus (green monkey) were collected from October to November 2018 from Bandia Reserve. Stool samples were processed using the merthiolate-iodine-formalin staining technique and the modified Ritchie method. The slides were examined under a microscope and the identification of parasites was based on the morphology of protozoan cysts and helminth eggs. The analysis of data was conducted using R version 3.4.3 with p=0.05. Results: A total of six species of parasites were found, including five protozoa (Entamoeba coli, Entamoeba histolytica/ dispar, Entamoeba hartmanni, Endolimax nana, and Iodamoeba butschlii) and one nematode (Strongyloides spp.). The overall prevalence of gastrointestinal parasite was 76.2% (95% CI: 69.7%-82.7%). Two parasites with zoonotic potential, mainly E. histolytica/dispar with a prevalence of 13.4% (95% CI: 8.2%-18.6%) and Strongyloides spp. with a prevalence of 6.7% (95% CI: 2.9%-10.5%), were found. Conclusion: This study indicated that the monkeys of the Bandia Reserve are infested by zoonotic parasites and can, therefore, ensure transmission to visitors to the Reserve. The parasitological data that we report are the first available for these species of monkeys in the Bandia Reserve.


2009 ◽  
Vol 46 (4) ◽  
pp. 698-706 ◽  
Author(s):  
N. A. Twenhafel ◽  
D. A. Alves ◽  
B. K. Purcell

Tularemia, caused by Francisella tularensis, is a sporadic zoonotic disease with the potential to be an agent of biowarfare or bioterrorism. We describe here the gross, histologic, immunohistochemical, and ultrastructural findings in a group of 5 African green monkeys (AGMs) that received an average inhaled dose of 729 colony-forming units of F. tularensis and died or were euthanatized between days 7 and 11 post infection. Clinical changes were evident by 48 hours post infection, and key physiologic abnormalities included increases in body temperature, heart rate, peak cardiac pressure, and mean blood pressure. Prominent gross changes in all cases included numerous pinpoint to 1-cm, well-demarcated, necrotic foci present consistently in the lungs, mediastinal lymph nodes, and spleen but also seen in the heart, mediastinum, diaphragm, liver, urinary bladder, urethra, and mesentery. The lungs, mediastinal lymph nodes, and spleen were most severely affected, with as much as 50% of the tissue replaced by necrotic foci. Histologic changes in all tissues consisted of welldelineated foci of necrosis and neutrophilic and histiocytic inflammation, with varying amounts of hemorrhage, edema, fibrin, and vasculitis. Some lesions were immature pyogranulomas. Strong immunoreactivity was identified primarily within macrophages. Ultrastructurally, bacteria were present within cytoplasmic vacuoles of alveolar macrophages, many of which were degenerate. In summary, AGMs infected with F. tularensis by aerosol develop lethal multisystemic disease that particularly targets the lungs and lymphoid tissues. Thus, AGMs should serve as a suitable and reliable animal model for further studies of tularemia.


2021 ◽  
Author(s):  
Lori A Rowe ◽  
Brandon J Beddingfield ◽  
Kelly Goff ◽  
Stephanie Z Killeen ◽  
Nicole R Chirichella ◽  
...  

In recent months, several SARS-CoV-2 variants have emerged that enhance transmissibility and escape host humoral immunity. Hence, the tracking of viral evolutionary trajectories is clearly of great importance. Little is known about SARS-CoV-2 evolution in nonhuman primate models used to test vaccines and therapies and to model human disease. Viral RNA was sequenced from rectal swabs from Chlorocebus aethiops (African green monkeys) after experimental respiratory SARS-CoV-2 infection. Two distinct patterns of viral evolution were identified that were shared between all collected samples. First, mutations in the furin cleavage site that were initially present in the virus as a consequence of VeroE6 cell culture adaptation were subsequently lost in virus recovered in rectal swabs, confirming the necessity of this motif for viral infection in vivo. Three amino acid changes were also identified; ORF 1a S2103F, and spike D215G and H655Y, that were detected in rectal swabs from all sampled animals. These finding are demonstrative of intra-host SARS-CoV-2 evolution unique to this nonhuman primate species and identifies a host-adapted variant of SARS-CoV-2 that may be useful in future development of primate disease models.


2021 ◽  
Author(s):  
Alyssa C Fears ◽  
Brandon J Beddingfield ◽  
Nicole R Chirichella ◽  
Nadia Slisarenko ◽  
Stephanie Z Killeen ◽  
...  

The novel coronavirus SARS-CoV-2 has caused a worldwide pandemic resulting in widespread efforts in development of animal models that recapitulate human disease for evaluation of medical countermeasures, and to dissect COVID-19 immunopathogenesis. We tested whether route of experimental infection substantially changes COVID-19 disease characteristics in two species (Macaca mulatta; rhesus macaques; RM, Chlorocebus atheiops; African green monkeys; AGM) of nonhuman primates. Species-specific cohorts of RM and AGM Rhesus macaques (Macaca mulatta, RMs) and African green monkeys (Chlorocebus aethiops, AGMs) were experimentally infected with homologous SARS-CoV-2 by either direct mucosal instillation or small particle aerosol in route-discrete subcohorts. Both species demonstrated equivalent infection initially by either exposure route although the magnitude and duration of viral loading was greater in AGMs than that of the RM. Clinical onset was nearly immediate (+1dpi) in mucosally-exposed cohorts whereas aerosol-infected animals began to show signs +7dpi. Myeloid cell responses indicative of the development of pulmonary scarring and extended lack of regenerative capacity in the pulmonary compartment was a conserved pathologic response in both species by either exposure modality. This pathological commonality may be useful in future anti-fibrosis therapeutic evaluations and expands our understanding of how SARS-CoV-2 infection leads to ARDS and functional lung damage.


2005 ◽  
Vol 34 (3) ◽  
pp. 139-146 ◽  
Author(s):  
Roland Plesker ◽  
Udo Hetzel ◽  
Werner Schmidt

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