scholarly journals Laboratory Evaluation of Within-Species, Between-Species, and Parthenogenetic Reproduction in Reticulitermes Flavipes and Reticulitermes Virginicus

1981 ◽  
Vol 88 (1-2) ◽  
pp. 75-87 ◽  
Author(s):  
Ralph W. Howard ◽  
Eldon J. Mallette ◽  
Michael I. Haverty ◽  
Richard V. Smythe
2013 ◽  
Vol 63 (Pt_10) ◽  
pp. 3873-3876 ◽  
Author(s):  
Erick R. James ◽  
Vera Tai ◽  
Rudolf H. Scheffrahn ◽  
Patrick J. Keeling

Historically, symbiotic protists in termite hindguts have been considered to be the same species if they are morphologically similar, even if they are found in different host species. For example, the first-described hindgut and hypermastigote parabasalian, Trichonympha agilis (Leidy, 1877) has since been documented in six species of Reticulitermes, in addition to the original discovery in Reticulitermes flavipes. Here we revisit one of these, Reticulitermes virginicus, using molecular phylogenetic analysis from single-cell isolates and show that the Trichonympha in R. virginicus is distinct from isolates in the type host and describe this novel species as Trichonympha burlesque i n. sp. We also show the molecular diversity of Trichonympha from the type host R. flavipes is greater than supposed, itself probably representing more than one species. All of this is consistent with recent data suggesting a major underestimate of termite symbiont diversity.


EDIS ◽  
1969 ◽  
Vol 2004 (5) ◽  
Author(s):  
Nan-Yao Su ◽  
Rudolf H. Scheffrahn ◽  
Brian Cabrera

Most pest species of subterranean termites in North America belong to the endemic genus Reticulitermes. Reticulitermes species are found in every state in the continental United States except Alaska, but are most common in the warm and humid southeastern region. The eastern subterranean termite, R. flavipes is the most widely distributed and is found in the entire eastern region of North America as far north as Ontario, Canada, and south to Key Largo, Florida. Its counterpart, the western subterranean termite, R. hesperus Banks, is found along the entire Pacific Coast ranging from southern California to British Columbia. Reticulitermes tibialis occurs in the inter-mountain region of the West. In addition to R. flavipes, two other Reticulitermes occur in Florida, R. virginicus, and R. hageni. This document is EENY-212, one of a series of Featured Creatures from the Entomology and Nematology Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Published: May 2001. EENY-212/IN369: Native Subterranean Termites: Reticulitermes flavipes (Kollar), Reticulitermes virginicus (Banks), Reticulitermes hageni Banks (Insecta: Isoptera: Rhinotermitidae) (ufl.edu)


2018 ◽  
Vol 74 (7) ◽  
pp. 1704-1710 ◽  
Author(s):  
Olanrewaju Raji ◽  
Juliet D Tang ◽  
Telmah Telmadarrehei ◽  
Dragica Jeremic

2010 ◽  
Vol 30 (03) ◽  
pp. 156-161 ◽  
Author(s):  
R. Gheisari ◽  
B. Bomke ◽  
T. Hoffmann ◽  
R. E. Scharf

SummaryWe have performed a monocenter study on 29 consecutive patients with acquired haemophilia A who were referred for diagnosis and treatment to the Düsseldorf Haemophilia Comprehensive Care Center between March 2001 and February 2010. Patients, methods: 18 men (age: 44–86 years) and 11 women (age: 20–83 years). For laboratory evaluation, a standardized staged protocol of aPTT, FVIII : C activity and concentration, mixing studies with patient and normal plasma, and quantification of inhibitor titers (Bethesda assay) was used. Diagnostic work-up included elaborate examinations for any underlying disease. Results: In 18 (62%) of the 29 patients with acquired haemophilia A, an underlying disorder was identified, including 9 patients with respiratory diseases (31%), 7 patients with autoimmune disorders (24%), one with malignancy, and one with postpartum state, while in 11 patients (38%) acquired haemophilia A remained idiopathic. Haemotherapy of bleeding, suppression or elimination of the inhibitor, and induction of immunotolerance to endogenous FVIII:C were performed according to a treatment algorithm. Predefined clinical endpoints were control of bleeding, eradication of the inhibitor, complete or partial remission (CR, PR), relapse, or early death (≤30 days). Of the 29 patients in total, 22 individuals achieved CR (76%), three had PR, one relapsed, and three died within 30 days (one of acute myocardial infarction while on anti-haemorrhagic treatment, one of sepsis while on immunosuppression due to active acquired haemophilia A, one of lung bleeding in association with pre-existing pulmonary sarcoidosis). Conclusion: This monocenter study demonstrates that control of life-threatening bleeding, eradication of the inhibitor, and induction of tolerance to endogenous FVIII have significantly improved the clinical outcome of acquired haemophilia A. Our data also suggest a shift in underlying disorders associated with acquired haemophilia A, whereby, in comparison to published studies, a relative increase in the proportion of patients with respiratory diseases is present.


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