Sublethal and Transgenerational Effects of Reduced-Risk Insecticides on Macrolophus basicornis (Hemiptera: Miridae).

Reduced-risk insecticides and mirid predators have been used to control Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) in tomato crops. However, even when causing low mortality to the beneficial insects, these products might cause side effects. This study investigated the sublethal and transgenerational effects of buprofezin, cyantraniliprole, and spiromesifen on Macrolophus basicornis (Stal) (Hemiptera: Miridae). After 72 h of exposure of third-instar nymphs and adults to residues on tomato leaves, adult couples were formed and kept in cages with residue-free tomato leaves. The leaves were changed every 48 h and the offspring were assessed in 6 different periods. Body size was assessed by measuring the hind-tibia length of adults (F0) from exposed nymphs and in three different offspring groups. None of the insecticide residues caused a reduction on offspring populations or affected the body size of adults in generation F0. Regardless, buprofezin and spiromesifen reduced the tibia length of adults (F1) from exposed nymphs assayed in the third mating period. Cyantraniliprole did not affect any parameter and could be recommended for control of B. tabaci in association with M. basicornis releases. This study may contribute to future field assays of the compatibility of these insecticides with M. basicornis.

Risk Assessment of Insecticides Used in Tomato to Control Whitefly on the Predator Macrolophus basicornis (Hemiptera: Miridae).

The generalist mirid predator Macrolophus basicornis may contribute to Integrated Pest Management (IPM) of Bemisia tabaci in tomato crops. It is important to know the compatibility of the chemicals used to control this pest with this promising biological control agent. Seven insecticides were tested to investigate their toxicity to the predator. For four of the products, the LC50 for adults were determined. Buprofezin, cyantraniliprole and spiromesifen did not cause lethality and were classified as harmless. Acetamiprid, bifenthrin, etofenprox + acetamiprid and pyriproxyfen + acetamiprid caused acute toxicity and were classified as harmful. LT50 for all harmful insecticides were relatively low, ranging from 1.8 to 3.2 days. Moreover, these four insecticides have low LC50, with acetamiprid (0.26 mg a.i. L-1) as the lowest, followed by bifenthrin (0.38 mg a.i. L-1), etofenprox + acetamiprid (4.80 mg a.i. L-1) and pyriproxyfen + acetamiprid (8.71 mg a.i. L-1). However, the calculated risk quotient (RQ) values demonstrated that these insecticides were mostly ecologically safe for this predator, except for acetamiprid, classified as slightly to moderately toxic. The present study can contribute to the use of M. basicornis as a biological control agent on tomato crops and to compatible use with the insecticides tested, according to IPM strategies.

In vitro leishmanicidal and cytotoxic activities of the glycoalkaloids from Solanum lycocarpum (Solanaceae) fruits.

Leishmaniasis is an infection caused by a protozoan parasite of the genus Leishmania and is the second most prevalent parasitic protozoal disease after malaria in the world. We report the in vitro leishmanicidal activity on promastigote forms of Leishmania amazonensis and cytotoxicity, using LLCMK2 cells, of the glycoalkaloids from the fruits of Solanum lycocarpum, determined by colorimetric methods. The alkaloidic extract was obtained by acid-base extraction; solamargine and solasonine were isolated by silica-gel chromatography, followed by reversed-phase HPLC final purification. The alkaloidic extract, solamargine, solasonine, as well as the equimolar mixture of the glycoalkaloids solamargine and solasonine displayed leishmanicidal activity against promastigote forms of L. amazonensis, whereas the aglycone solasodine was inactive. After 24 and 72 h of incubation, most of the samples showed lower cytotoxicities (IC50 6.5 to 124 µM) as compared to leishmanicidal activity (IC50 1.1 to 23.6 µM). The equimolar mixture solamargine/solasonine was the most active with an IC50 value of 1.1 µM, after 72 h. Likewise, solamargine was the most active after 24 h with an IC50 value of 14.4 µM, both in comparison with the positive control amphotericin B.