Release and establishment in Nigeria of Epidinocarsis lopezi, a parasitoid of the cassava mealybug, Phenacoccus manihoti

The encyrtid wasp Epidinocarsis (= Apoanagyrus) lopezi (De Santis) was imported from Paraguay into Nigeria for the biological control of the cassava mealybug, Phenacoccus manihoti Matile-Ferrero. It was mass-reared and released at four localities in Nigeria. The parasitoid is now established and it is dispersing throughout cassava growing areas of Nigeria.

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Libération et installation au Nigéria d'Epidinocarsis lopezi, parasitoïde de la cochenille du manioc Phenococcus manihoti

Résumé Epidinocarsis lopezi (Apoanagyrus) lopezi a été introduit du Paraguay au Nigéria pour lutter contre la cochenille du manioc, Phenacoccus manihoti. Il a été lâché dans quatre champs de manioc pour étudier son acclimatation et son installation au Nigéria. Trois ans après les lâchers, les résultats ont permis de conclure que E. lopezi s'est établi avec succès et se disperse dans la plupart des zones de culture du manioc au Nigeria; il a aussi survécu à trois saisons pluvieuses pendant lesquelles les populations de P. manihoti ont été très faibles. Quatorze mois après les premiers lâchers, cet encyrtide a été obtenu à environ 150 km du lieu de libération.

     

A short-oligonucleotide microarray that allows improved detection of gastrointestinal tract microbial communities

Background  

The human gastrointestinal (GI) tract contains a diverse collection of bacteria, most of which are unculturable by conventional microbiological methods. Increasingly molecular profiling techniques are being employed to examine this complex microbial community. The purpose of this study was to develop a microarray technique based on 16S ribosomal gene sequences for rapidly monitoring the microbial population of the GI tract.     

Interference with heparin binding and oligomerization creates a novel anti-inflammatory strategy targeting the chemokine system

A hallmark of autoimmunity and other chronic diseases is the overexpression of chemokines resulting in a detrimental local accumulation of proinflammatory immune cells. Chemokines play a pivotal role in cellular recruitment through interactions with both cell surface receptors and glycosaminoglycans (GAGs). Anti-inflammatory strategies aimed at neutralizing the chemokine system have to-date targeted inhibition of the receptor-ligand interaction with receptor antagonists. In this study, we describe a novel strategy to modulate the inflammatory process in vivo through mutation of the essential heparin-binding site of a proinflammatory chemokine, which abrogates the ability of the protein to form higher-order oligomers, but retains receptor activation. Using well-established protocols to induce inflammatory cell recruitment into the peritoneal cavity, bronchoalveolar air spaces, and CNS in mice, this non-GAG binding variant of RANTES/CCL5 designated [44AANA47]-RANTES demonstrated potent inhibitory capacity. Through a combination of techniques in vitro and in vivo, [44AANA47]-RANTES appears to act as a dominant-negative inhibitor for endogenous RANTES, thereby impairing cellular recruitment, not through a mechanism of desensitization. [44AANA47]-RANTES is unable to form higher-order oligomers (necessary for the biological activity of RANTES in vivo) and importantly forms nonfunctional heterodimers with the parent chemokine, RANTES. Therefore, although retaining receptor-binding capacity, altering the GAG-associated interactive site of a proinflammatory chemokine renders it a dominant-negative inhibitor, suggesting a powerful novel approach to generate disease-modifying anti-inflammatory reagents.     

Complex binding interactions between multicomponent mixtures and odorant receptors in the olfactory organ of the Caribbean spiny lobster Panulirus argus

Our study was designed to examine how components of complex mixtures caninhibit the binding of other components to receptor sites in the olfactorysystem of the spiny lobster Panulirus argus. Biochemical binding assayswere used to study how two- to six-component mixtures inhibit binding ofthe radiolabeled odorants taurine, L-glutamate andadenosine-5'-monophosphate to a tissue fraction rich in dendritic membraneof olfactory receptor neurons. Our results indicate that binding inhibitionby mixtures can be large and is dependent on the nature of the odorantligand and on the concentration and composition of the mixture. The bindinginhibition by mixtures of structurally related components was generallypredicted using a competitive binding model and binding inhibition data forthe individual components. This was not the case for binding inhibition bymost mixtures of structurally unrelated odorants. The binding inhibitionfor these mixtures was generally smaller than that for one or more of theircomponents, indicating that complex binding interactions between componentscan reduce their ability to inhibit binding. The magnitude of bindinginhibition was influenced more by the mixture's precise composition than bythe number of components in it, since mixtures with few components weresometimes more inhibitory than mixtures with more components. Thesefindings raise the possibility that complex binding interactions betweencomponents of a mixture and their receptors may shape the output ofolfactory receptor neurons to complex mixtures.     

Population genetics of sexually antagonistic mitochondrial mutants under inbreeding

In random mating populations, the fate of mitochondrial mutations with sexually antagonistic effects in males and females is based solely on their effects in females. Therefore, mitochondrial mutations that are beneficial for females but deleterious for males will be fixed in a deterministic model. Why then are males not less fertile? One among many several explanations is that inbreeding limits the ability of mutants to spread since the fitness of a mother is now linked to her son's fertility. We model this situation analytically and determine conditions under which such sexually antagonistic mitochondrial mutants can spread and fix in a population. We also provide alternative hypotheses for the lack of observed male sterility in natural populations.     

Bi-Epitope SPR Surfaces: A Solution to Develop Robust Immunoassays

Surface plasmon resonance (SPR)-based immunoassays have numerous applications and require high affinity reagents for sensitive and reliable measurements. We describe a quick approach to turn low affinity antibodies into appropriate capture reagents. We used antibodies recognizing human ephrin type A receptor 2 (EphA2) and a ProteOn XPR36 as a model system. We generated so-called ‘bi-epitope’ sensor surfaces by immobilizing various pairs of anti-EphA2 antibodies using standard amine coupling. The apparent binding affinities to EphA2 and EphA2 detection sensitivities of the bi-epitope and ‘single-epitope’ surfaces were then compared. For all antibody pairs tested, bi-epitope surfaces exhibited an ∼10–100-fold improvement in apparent binding affinities when compared with single-epitope ones. When pairing 2 antibodies of low intrinsic binding affinities (∼10⁻⁸ M) and fast dissociation rates (∼10⁻² s⁻¹), the apparent binding affinity and dissociation rate of the bi-epitope surface was improved up to ∼10^–10 M and 10⁻⁴ s⁻¹, respectively. This led to an ∼100–200-fold enhancement in EphA2 limit of detection in crude cell supernatants. Our results show that the use of antibody mixtures in SPR applications constitutes a powerful approach to develop sensitive immunoassays, as previously shown for non-SPR formats. As SPR-based assays have significantly expanded their reach in the last decade, such an approach promises to further accelerate their development.     

Establishment of the neotropical predator Amblyseius idaeus (Acari: Phytoseiidae) in Benin,West Africa

Populations of the phytoseiid predator Amblyseius(=Neoseiulus) idaeus (Denmark & Muma) from northeastern Brazil, have been successfully introduced into Benin, West Africa, as part of a classical biological control campaign to control the exotic cassava green mite Mononychellus tanajoa (Bondar). Monthly follow‐up surveys revealed the presence of A. idaeus in most release sites. Some populations have persisted for at least 18 months, including two cycles of potentially limiting wet and dry season conditions. In some sites A. idaeus has been the numerically dominant phytoseiid predator on cassava Manihot esculenta, where it is associated with the tetranychids M. tanajoa and Oligonychus gossypii Zacher. During periods of low M. tanajoa densities A. idaeus disappeared from cassava, but were found on weeds with O. gossypii until prey densities on cassava increased.