Loxosceles Laeta Research Articles

Binding of green tea epigallocatechin gallate to the arginine kinase active site from the brown recluse spider (Loxosceles laeta): A potential synergist to chemical pesticides

Loxosceles spp. spiders can cause serious public health issues. Chemical control is commonly used, leading to health and environmental problems. Identifying molecular targets and using them with natural compounds can help develop safer and eco-friendlier biopesticides. We studied the kinetics and predicted structural characteristics of arginine kinase (EC 2.7.3.3) from Loxosceles laeta (LlAK), a key enzyme in the energy metabolism of these organisms. Additionally, we explored (−)-epigallocatechin gallate (EGCG), a green tea flavonoid, as a potential lead compound for the LlAK active site through fluorescence and in silico analysis, such as molecular docking and molecular dynamics (MD) simulation and MM/PBSA analyses. The results indicate that LlAK is a highly efficient enzyme (KmArg 0.14 mM, KmATP 0.98 mM, kcat 93 s−1, kcat/KmArg 630 s−1 mM−1, kcat/KmATP 94 s−1 mM−1), which correlates with its structure similarity to others AKs (such as Litopenaeus vannamei, Polybetes pythagoricus, and Rhipicephalus sanguineus) and might be related to its important function in the spider's energetic metabolism. Furthermore, the MD and MM/PBSA analysis suggests that EGCG interacted with LlAK, specifically at ATP/ADP binding site (RMSD <1 nm) and its interaction is energetically favored for its binding stability (−40 to −15 kcal/mol). Moreover, these results are supported by fluorescence quenching analysis (Kd 58.3 μM and Ka 1.71 × 104 M-1). In this context, LlAK is a promising target for the chemical control of L. laeta, and EGCG could be used in combination with conventional pesticides to manage the population of Loxosceles species in urban areas.

Evaluating thermal niche overlap of a predator–prey system: Do spiders choose suboptimal temperatures in pursuit of prey?

AbstractEctotherm predators and their prey could potentially respond differently to habitat temperatures. Predators might select higher temperatures to increase their probability of capture while prey could select lower or higher temperatures that may enhance their escape capability. We used a combination of field and laboratory analyses to characterise the thermal niches of predator species and their potential arthropod prey. We studied a predator–prey system in northern Chile using a common desert‐dwelling spider Loxosceles laeta and three potential prey: a tenebrionid beetle Psammetichus costatus (Coleoptera), Pycnoscelus surinamensis (Blattodea) and Porcellio laevis (Isopoda). Results showed that the predator L. laeta selects warmer temperatures (Tp = 27.22 ± 4.87°C) in laboratory and lower temperatures in field conditions (Ts = 20.8 ± 1.59°C), with low temperatures in the morning and high temperatures at night. The three prey species had lower and different preferred temperatures than the predator in laboratory conditions. However, we found a high overlap in the thermal niche between the predator and their prey in field conditions, whereby the predator selected similar temperatures to its prey, one exception being P. laevis that chooses completely different habitat temperatures. This suggests that predators look for their prey in places with low temperatures that are not thermally suitable for them, whereas the prey may use this strategy of selecting low temperatures to evade potential predators.

Identification of a common epitope in knottins and phospholipases D present in Loxosceles sp venom by a monoclonal antibody

In the Americas and specially in Brazil, the Loxosceles intermedia, Loxosceles gaucho and Loxosceles laeta are the three most medically relevant brown spider species, and whose bites can lead to the condition known as loxoscelism. Here, we report the development of a tool capable of identifying a common epitope amongst Loxosceles sp. venom's toxins. A murine monoclonal antibody (LmAb12) and its recombinant fragments (scFv12P and diabody12P) have been produced and characterized. This antibody and its recombinant constructs were able to recognize proteins of Loxosceles spider venoms with specificity. The scFv12P variant was also able to detect low concentrations of Loxosceles venom in a competitive ELISA assay, displaying potential as a venom identification tool. The primary antigenic target of LmAb12 is a knottin, a venom neurotoxin, that has a shared identity of 100 % between the L. intermedia and L. gaucho species and high similarity to L. laeta. Furthermore, we observed LmAb12 was able to partially inhibit in vitro hemolysis, a cellular event typically induced by the Loxosceles sp. venoms. Such behavior might be due to LmAb12 cross-reactivity between the antigenic target of LmAb12 and the venom's dermonecrotic toxins, the PLDs, or even the existence of synergism between these two toxins.

The synanthropic austral-most record of the species Loxosceles hirsuta and the formal record of Loxosceles laeta (Araneae: Sicariidae)

A formal record of the medically important species Loxosceles laeta (Nicolet, 1849) and new records of Loxosceles hirsuta Mello-Leitão, 1931 (Araneae: Sicariidae) are provided for La Pampa province, Argentina, comprising its southernmost record. The specimens of L. hirsuta in this work were found inhabiting human structures and were collected in different localities, between long time lapses, which suggests that L. hirsuta much like L. laeta is highly synanthropic and established in La Pampa.

Analysis of NGS data from Peruvian Loxosceles laeta spider venom gland reveals toxin diversity

Accidents involving spiders from the genus Loxosceles cause medical emergencies in several countries of South America. The species Loxosceles laeta is ubiquitously present in Peru and is responsible for severe accidents in this country. To further characterize L. laeta venom components and to unveil possible variations in the Peruvian population, we provide an overview of the toxins-related transcripts present in the venom gland of Peruvian L. laeta. A dataset from a cDNA library previously sequenced by MiSeq sequencer (Illumina) was re-analyzed and the obtained data was compared with available sequences from Loxosceles toxins. Phospholipase-D represent the majority (69,28 %) of the transcripts related to venom toxins, followed by metalloproteases (20,72 %), sicaritoxins (6,03 %), serine-proteases (2,28 %), hyaluronidases (1,80 %) and Translationally Controlled Tumor Protein (TCTP) (0,56 %). New sequences of phospholipases D,sicaritoxins, hyaluronidase, TCTP and serine proteinases were described. Differences between the here-described toxin sequences and others, previously identified in venom glands from other spiders, were visualized upon sequence alignments. In addition, an in vitro hyaluronidase activity assay was also performed to complement comparisons between Peruvian and Brazilian L. laeta venom enzymatic activities, revealing a superior activity in the venom from Brazilian specimens. These new data provide a molecular basis that can help to explain the difference in toxicity among L. laeta venoms from different countries in South America.

Multi-Point Nanoindentation Method to Determine Mechanical Anisotropy in Nanofibrillar Thin Films.

Biomaterials with outstanding mechanical properties, including spider silk, wood, and cartilage, often feature an oriented nanofibrillar structure. The orientation of nanofibrils gives rise to a significant mechanical anisotropy, which is extremely challenging to characterize, especially for microscopically small or inhomogeneous samples. Here, a technique utilizing atomic force microscope indentation at multiple points combined with finite element analysis to sample the mechanical anisotropy of a thin film in a microscopically small area is reported. The system studied here is the tape-like silk of the Chilean recluse spider, which entirely consists of strictly oriented nanofibrils giving rise to a large mechanical anisotropy. The most detailed directional nanoscale structure-property characterization of spider silk to date is presented, revealing the tensile and transverse elastic moduli as 9 and 1GPa, respectively, and the binding strength between silk nanofibrils as 159 ± 13MPa. Furthermore, based on this binding strength, the nanofibrils' surface energy is derived as 37 mJ m-2 , and concludes that van der Waals forces play a decisive role in interfibrillar binding. Due to its versatility, this technique has many potential applications, including early disease diagnostics, as underlying pathological conditions can alter the local mechanical properties of tissues.

Partial in vivo protection against Peruvian spider Loxosceles laeta venom by immunization with a multiepitopic protein (rMEPLox)

Loxoscelism is a serious public health problem in Peru, with approximately 2500 accidents reported per year. To envision alternatives to cope with this health problem, the neutralizing humoral immune response against the lethal effects of Peruvian spider Loxosceles laeta venom was evaluated in a mouse model by immunization with a non-toxic multiepitopic protein (rMEPLox). This immunogen contains epitopes from an astacin-like metalloprotease, a hyaluronidase and a sphingomyelinase-D from Loxosceles intermedia and from SMase-I from L. laeta venoms. In vivo protection assays showed that five out of six mice immunized with rMEPLox (after six injections) resisted to 1.4 LD50 of L. laeta venom, whereas only two animals from a control group survived. The present results indicates that this multiepitopic protein can be a promising candidate for anti-loxoscelic antivenom production and experimental vaccination approaches.

Specificity of Loxosceles α clade phospholipase D enzymes for choline-containing lipids: Role of a conserved aromatic cage.

Spider venom GDPD-like phospholipases D (SicTox) have been identified to be one of the major toxins in recluse spider venom. They are divided into two major clades: the α clade and the β clade. Most α clade toxins present high activity against lipids with choline head groups such as sphingomyelin, while activities in β clade toxins vary and include preference for substrates containing ethanolamine headgroups (Sicarius terrosus, St_βIB1). A structural comparison of available structures of phospholipases D (PLDs) reveals a conserved aromatic cage in the α clade. To test the potential influence of the aromatic cage on membrane-lipid specificity we performed molecular dynamics (MD) simulations of the binding of several PLDs onto lipid bilayers containing choline headgroups; two SicTox from the α clade, Loxosceles intermedia αIA1 (Li_αIA) and Loxosceles laeta αIII1 (Ll_αIII1), and one from the β clade, St_βIB1. The simulation results reveal that the aromatic cage captures a choline-headgroup and suggest that the cage plays a major role in lipid specificity. We also simulated an engineered St_βIB1, where we introduced the aromatic cage, and this led to binding with choline-containing lipids. Moreover, a multiple sequence alignment revealed the conservation of the aromatic cage among the α clade PLDs. Here, we confirmed that the i-face of α and β clade PLDs is involved in their binding to choline and ethanolamine-containing bilayers, respectively. Furthermore, our results suggest a major role in choline lipid recognition of the aromatic cage of the α clade PLDs. The MD simulation results are supported by in vitro liposome binding assay experiments.

Self-strengthening tape junctions inspired by recluse spider webs.

Adhesive tapes are versatile and widely used yet lack adhesion strength due to their tendency to fail via peeling, a weak failure mode. A tape with surprising adhesive properties is the recluse spider's 50 nm-thin silk ribbon with a 1 : 150 aspect ratio. Junctions of these microscopic sticky tapes can withstand the material's tensile failure stress of ≈1 GPa. We modeled these natural tape-tape junctions and revealed a bi-modal failure behavior, critically dependent on the two tapes' intersection angle. One mode leads to regular, low-strength peeling failure, while the other causes the junction to self-strengthen, eliminating the inherent weakness in peeling. This self-strengthening mechanism locks the two tapes together, increasing the junction strength by 550% and allowing some junctions to remain intact after tensile failure. This impressive adhesive strength of tapes has never before been observed or predicted. We found that recluse spiders make tape junctions with pre-stress to force the locked, high-strength failure mode. We used this approach to make junctions with synthetic adhesive tapes that overcame the weak peeling failure.

Avaliação de células mesenquimais e dapsona para o tratamento de feridas dermonecróticas causadas pelo veneno de Loxosceles laeta em coelhos

Abstract This study aimed to evaluate the efficacy of mesenchymal stem cells (MSC), alone or associated with dapsone (DAP), in treating dermonecrotic wounds caused by Loxosceles laeta venom. Twenty-five male rabbits were distributed into five groups. Negative control received ultrapure water (C-), whilst all other groups were injected with 20 μg of L. laeta venom. After 4 hours, each group received one of the following treatments: PBS (C+), DAP, MSC, and DAP+MSC. Animals were evaluated daily and photographic records made for analysis of wound area. Twelve days after, animals were euthanized and skin samples removed for histological analysis. We observed that DAP showed the best percentage of wound contraction at day 3. In the treatments using MSCs, a negative value of wound contraction was observed for the isolated MSCs, as well as a lower contraction value for the association of the MSC + DAP when compared to PBS, probably, by the increase in initial infammation after the application of stem cells, due to the fact that MSCs secrete a broad spectrum of bioactive molecules such as cytokines and growth factors that favor regeneration. Histologically, it was observed that animals of C+ showed extensive areas of necrosis, ulcers, neutrophilic infiltrate, and mineralization. Collagen deposition showed increase in MSC+DAP treatment, however vascularization remained unchanged. This is the first report using MSC and MSC+DAP as a treatment for cutaneous loxoscelism and more studies are needed to determine its use as an alternative therapy for dermonecrotic lesions caused by Loxosceles spider.

Effects of food, kinship, and density on the longevity of spiderlings

Cannibalism is a behavioral characteristic found in a wide variety of animal groups. Although the rates of cannibalism can vary from one group to another, studies indicate that the main factors contributing to an increase in the frequency of such behavior are the availability of food, population density, the behavior and availability of victims, and environmental stress. We carried out different laboratory experiments to assess whether different factors such as the presence or absence of food among siblings and non-siblings, and at different densities among conspecific and heterospecific individuals, affect longevity of recently emerged Brazilian brown recluse (Loxosceles intermedia Mello-Leitão, 1934) and Chilean recluse (Loxosceles laeta (Nicolet, 1849)) spiderlings during periods of starvation. The results revealed that the survivorship of L. laeta during starvation was significantly higher than that of L. intermedia and that the addition of conspecific individuals increased survival rates by 1.5- and 1.6-fold, respectively. The tolerance of conspecifics differed between the two species, and generally, cannibalism was not observed, probably due to the risk of predation and limited consumption by weakened spiders, which coincided with the continued availability of endogenous vitelline reserves, thus indicating that the use of these spiderlings as a food resource may act to regulate starvation in more resistant spiders. The greater longevity and conspecific tolerance of L. laeta may be important factors contributing to the establishment of large populations of this spider in restricted areas, whereas for L. intermedia, hunger probably functions as a trigger for dispersal.

Ecological niche divergence between the brown recluse spiders Loxosceles laeta and L. surca (Sicariidae) in Chile

ABSTRACT The laeta species group is the main source of Loxosceles species in Chile, a genus of medical importance due to the cytotoxic properties of its venom and the synanthropic habits of its dominant species, Loxosceles laeta. However, a poorly studied, cryptic, and putative sister species, Loxosceles surca, is also known to live in Chile at latitudes that overlap with L. laeta. In contrast to L. laeta, L. surca lives in natural areas away from humans. We used DNA sequences from L. surca to infer the phylogenetic history of this species and its congenerics. Additionally, we used ecological niche modelling to define the ecology of this species in contrast to its sister species. Our results show that L. surca does, indeed, belong to the laeta species group, and is likely a sister species to L. laeta. Although these species are fairly cryptic with respect to each other, the substantial genetic divergence between them is consistent with other distinct sister species in this genus. The laeta group is also sister to the large reclusa group that radiated into the Caribbean, Central, and North America. The phylogeny further supports the contention that L. diaguita belongs in its own species group separate from laeta. Our ecological niche analysis shows that L. surca and L. laeta have distinctly different allopatric habitats, and we suggest that these differences explain why one species became synanthropic, while the other did not.

Specificity of Loxosceles α Clade Phospholipase D Enzymes for Choline-Containing Lipids: Role of a Conserved Aromatic Cage

Phospholipase D (PLD) enzymes are one of the major toxins in the recluse spider (genus Loxosceles) venom. Loxosceles PLD enzymes are classified in either the α clade or the β clade, and some correlation exists between α or β clade membership and high or low catalytic activity against sphingomyelin (SM), respectively. Lajoie et al., recently showed that a β clade enzyme from Sicarius terrosus (St_βID1) had a strong preference for substrates containing ethanolamine headgroups, and suggested that this substrate specificity originated from the interactions between the PLD interfacial face and lipids. To further understand the substrate specificity of these enzymes, we performed simulations of two PLDs from the α clade, Loxosceles intermedia αIA1 (Li_αIA1) and Loxosceles laeta αIII1 (Ll_αIII1), and one from the β clade, St_βIB1i. Simulations were performed in the presence of two types of lipid bilayers, choline-containing and ethanolamine-containing bilayer. We observed that the two α clade PLDs bound to bilayers with choline-containing lipids (PC or SM) using the catalytic loop. By contrast, St_ βIB1i, did not bind to those bilayers. Analyses of the trajectories also reveal the importance, for the two α clade PLDs, of three aromatic residues located on the catalytic loop and forming a π-cage interacting with a choline group. A multiple sequence alignment of 18 PLDs of both clades reveal that the aromatic cage is conserved in α clade PLDs and absent from at least one major subgroup of the β clade enzymes. We suggest that this cage controls the affinity for choline headgroups, which is in agreement with earlier reports of PC lipid headgroups interacting with aromatic amino acids.

Searching for the toxic potential of Loxosceles amazonica and Loxosceles willianilsoni spiders’ venoms

The Loxosceles genus belongs to the Sicariidae family and it comprises species whose venom can cause accidents with potentially fatal consequences. We have previously shown that SMase D is the enzyme responsible for the main pathological effects of Loxosceles venom. Despite the severity of accidents with Loxosceles, few species are considered to be of medical importance. Little is known about the venom of non-synanthropic species that live in natural environments. To contribute to a better understanding about the venom's toxicity of Loxosceles genus, the aim of this study was to (i) characterize the toxic properties of Loxosceles amazonica from two different localities and a recent described cave species Loxosceles willianilsoni and (ii) compare these venoms with that from Loxosceles laeta, which is among the most toxic ones. We show here that both L. amazonica venoms (from the two studied locations) and L. willianilsoni presented SMase D activity similar to that exhibited by L. laeta venom. Although L. amazonica and L. willianilsoni venoms were able to induce complement dependent human erythrocytes lysis, they were not able to induce cell death of human keratinocytes, as promoted by L. laeta venom, in the concentrations tested. These results indicate that other species of Loxosceles, in addition to those classified as medically important, have toxic potential to cause accidents in humans, despite interspecific variations that denote possible less toxicity.

Cytotoxic and genotoxic effects on human keratinocytes triggered by sphingomyelinase D from Loxosceles venom.

The spiders of the Loxosceles genus (called brown or violin spiders) are of medical relevance in several countries due to the many human envenomation cases reported. The main component of Loxosceles venom is the enzyme sphingomyelinase D (SMase D), which is responsible for the local and systemic effects induced by the whole venom. Here, we investigated the cytotoxic and genotoxic effects caused by Loxosceles laeta venom and SMase D on human keratinocytes to better understand the dermonecrosis development mechanism. Our findings indicate that whole venom, as well as SMase D, increases intracellular superoxide levels, leading to DNA damage. These effects appear to be dependent on the binding of SMase D to the cell surface, although the complete pathway triggered as a result of the binding still needs to be elucidated. Moreover, after SMase D treatment, we observed the presence of histone γH2AX, suggesting that the cells are undergoing DNA repair. Moreover, when ATR kinase was inhibited, the cell viability of human keratinocytes was decreased. Together, our findings strongly suggest that L. laeta venom, as well as SMase D, increases intracellular superoxide levels, leading to DNA damage in human keratinocytes. Additionally, the induced DNA damage is repaired through the activation of an apparent ATR-mediated DNA-damage response. This knowledge may contribute to a better understanding of the behaviour of human keratinocytes during cutaneous loxoscelism, a condition that affects thousands of people around the world.

The recent expansion of Chilean recluse Loxosceles laeta (Nicolet) (Arachnida: Araneae) in Southern Patagonia

The recent expansion of the Chilean recluse Loxosceles laeta (Nicolet, 1849) in southern Patagonia is commented and discussed in the light of current global change. New records are provided from both Región de Aysén and Región de Magallanes. In addition, Isla Dawson in Magallanes is the southernmost record for a sicariid spider in South America. Identification tips for health providers are included

Engineered antigen containing epitopes from Loxosceles spp. spider toxins induces a monoclonal antibody (Lox-mAb3) against astacin-like metalloproteases

Loxoscelism pose a health issue in the South America. The treatment for these accidents is based on the administration of antivenom produced in animals immunized with Loxosceles venom. In this work, a previously produced non-toxic multiepitopic chimeric protein (rMEPlox), composed of epitopes derived from the main toxins families (sphyngomielinase-D, metalloproteases, and hyaluronidases) of Loxosceles spider venoms, was used as antigen to produce monoclonal antibodies (mAbs). A selected anti-rMEPlox mAb (Lox-mAb3) reacted with metalloprotease from L. intermedia venom and showed cross-reactivity with metalloproteses from Brazilian and Peruvian Loxosceles laeta and Loxosceles gaucho venoms in immunoassays. The sequence recognized by Lox-mAb3 (184ENNTRTIGPFDYDSIMLYGAY205) corresponds to the C-terminal region of Astacin-like metalloprotease 1 and the amino acid sequence IGPFDYDSI, conserved among the homologs metalloproteases sequences, is important for antibody recognition. Lox-mAb3 neutralizes the fibrinogenolytic activity caused by metalloprotease from L. intermedia spider venom in vitro, which may lead to a decrease in hemorrhagic disturbances caused by Loxosceles envenomation. Our results show, for the first time, the use of a non-toxic multiepitopic protein for the production of a neutralizing monoclonal antibody against a metalloprotease of medically important Loxosceles venoms. These results contribute for the production improvement of therapeutic antivenom against loxoscelism.

Efficient expression and purification of recombinant Sphingomyelinase D from Loxosceles laeta in lepidopteran larvae as a candidate for antiserum production

Efficient expression and purification of recombinant Sphingomyelinase D from Loxosceles laeta in lepidopteran larvae as a candidate for antiserum production

Diversity of astacin-like metalloproteases identified by transcriptomic analysis in Peruvian Loxosceles laeta spider venom and in vitro activity characterization

Loxosceles spiders are found in almost all countries of South America. In Peru, Loxosceles laeta species is the main responsible for the accidents caused by poisonous animals, being known as “killer spiders”, due to the large number of fatal accidents observed. Astacin-like metalloproteases, named LALPs (Loxosceles astacin-like metalloproteases) are highly expressed in Loxosceles spiders venom gland. These proteases may be involved in hemorrhage and venom spreading, being relevant to the envenoming proccess. Thus, the aim of this work was to analyze Peruvian L. laeta venom gland transcripts using bioinformatics tools, focusing on LALPs. A cDNA library from Peruvian L. laeta venom glands was constructed and sequenced by MiSeq (Illumina) sequencer. After assembly, the resulting sequences were annotated, seeking out for similarity with previously described LALPs. Nine possible LALPs isoforms from Peruvian L. laeta venom were identified and the results were validated by in silico and in vitro experiments. This study contributes to a better understanding of the molecular diversity of Loxosceles venom and provide insights about the action of LALPs.

Loxoscelismo cutáneo-viscero-hemolítico con fallo renal agudo

The Loxoscelism is caused by the bite of spider Loxosceles laeta gender, of worldwide distribution. The poisoning can cause lesions dermonecrotic and less frequently a systemic illness that can be fatal.The mechanism of venom action is multifactorial. The characteristic dermonecrotic lesion results from the direct effects of the venom on the celular and basal membrane components , as well as the extracelular matrix.The initial interaction between the poison and tissues, causes complement activation , migration of polymorphic neutrophils, liberation of proteolytic enzymes, cytoquines, aggregation platelet, and blood flow alterations that result in edema and ischemia, with development of necrosis. There is no a definitive treatment for loxoscelism. However, the value of specific antivenom, to decrease lesion size and limit systemic illness even when such administration is delayed. We present a case of cutaneous-visceral loxoscelismo with unfavorable evolution.