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28 November 2022 Effect of relative humidity on the efficacy of entomopathogen Beauveria bassiana-based mycopesticide against red spider mite Tetranychus macfarlanei
MD. Nahian-Al Sabri, Mahbuba Jahan, Tetsuo Gotoh, İsmail Döker, Mohammad Shaef Ullah
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Tetranychus macfarlanei is a potential threat to various economically important crops. Chemical control is widely used to control this spider mite, but the exclusive reliance on chemical acaricides is now being questioned, and entomopathogens are emerging as a promising alternative. The efficacy of the entomopathogens largely depends on abiotic factors like temperature, humidity, rainfall etc. The experiments were conducted to determine the effect of relative humidity on the efficacy of the entomopathogen Beauveria bassiana (strain GHA), marketed as BotaniGard ES, against the adult female and egg stages of T. macfarlanei under laboratory conditions. Adult females and eggs of T. macfarlanei were treated with three concentrations of BotaniGard (1×106, 1×107, and 1×108 conidia/ml), and virulence was assessed on mites held at three relative humidity levels (55, 75, and 95 ± 2% RH) at 25 ± 1 °C. The results showed that the mortalities of adult females and eggs of T. macfarlanei were dose-dependent, and there is certainly a synergistic effect of relative humidity on the efficacy. When the eggs were treated under the above laboratory conditions, highest egg mortalities of 86.4 and 91% were recorded at a concentration of 1×108 conidia/mL at 75 and 95 ± 2% RH, respectively, after six days of treatment. The LT50 values on adult females were 28.7 h and 33.4 h at 95 and 75 ± 2% RH in a concentration of 1×108 conidia/ml, respectively, which was significantly lower than values for other concentrations and RH levels. This study identified 1×108 conidia/ml of B. bassiana at 75 to 95 ± 2% RH as the best possible combination than other lower RH to manage the spider mite.


Tetranychus macfarlanei Baker and Pritchard is a cosmopolitan pest. It is distributed in Afrotropical, Oriental, and Palearctic regions in different countries such as Bangladesh, the Canary Islands, China, India, Malaysia, Madagascar, Mauritius, the Phillippines, and Thailand (Ullah et al. 2021; Migeon & Dorkeld 2022). Because of its' phytophagous nature, it infests a wide range of economically important crops belonging to the families Malvaceae, Fabaceae, Cucurbitaceae, Convolvulaceae, and Solanaceae (Jeppson et al. 1975; Bolland et al. 1998). Tetranychus macfarlanei has arrived lately in Bangladesh, but in this short period, it has spread throughout the country, and is threatening many economically important crops, including jute, bean, eggplant, and bottle gourd (Ullah et al. 2012, 2021).

In Bangladesh, farmers have widely used insecticides and acaricides to control spider mites (Ullah & Gotoh 2013). However, chemical control seems to lose its' effectiveness, probably due to spider mites which may rapidly develop resistance to various acaricides after only a few applications (Whalon et al. 2021). Several unique biological characteristics of spider mites such as rapid population growth, high fecundity, and arrhenotokous reproduction contribute to their rapid development of acaricide resistance (Van Leeuwen et al. 2009). The Arthropod Pesticide Resistance Database (APRD) reports nearly 977 cases of acaricide resistance in phytophagous mites from the family Tetranychidae (Mota-Sanchez & Wise 2022). Therefore, sole dependence on insecticides is not a sustainable option for controlling tetranychids. To overcome the resistance problem, farmers increase spraying. Consequently, problems like high spraying costs, environmental pollution, and adverse effects on beneficial organisms may occur. The application of microbial pathogens, especially entomopathogenic fungi, is a promising alternative for successful pest management. Moreover, the mites do not develop resistance against fungi. They also have no toxic effects on environment, and have the potential for future biotechnological developments (Al Khoury et al. 2019, 2020).

Fungal entomopathogens have been performing well for several decades to get established as an important component in pest management programs worldwide (Lacey et al. 2015). About 700 species in 90 genera have been considered insect-pathogenic fungi (Khachatourians & Qazi 2008). Some of the most commonly studied fungal species are Beauveria bassiana (Balsamo) Vuillemin, Cordyceps fumosorosea (Wize) Kepler, B. Shrestha & Spatafora (previously known as Isaria fumosorosea Wize), Metarhizium anisopliae (Metschnikoff) Sorokin, and Lecanicillium lecanii (Zimmerman) Viegas (Li et al. 2011; Chen et al. 2015).

Beauveria bassiana has gained much popularity as a biological control agent for many insect pests, including ticks and mites, throughout the world (Chandler et al. 2000). However, its potential as a mycoacaricide has caught attention recently (Tamai et al. 1999, 2002). It has been an effective pathogen against many arthropod pests, including spider mites (Faria & Wraight 2001; Feng et al. 2004; Hatting et al. 2004; Pu et al. 2005; Ullah & Lim 2015). The repeated application of this fungal entomopathogen causes detrimental effects on certain arthropod pests and, thus, keeps the pest population under control (Groden et al. 2002). However, different strains of B. bassiana were found effective against spider mites (Chandler et al. 2005). The efficacy of B. bassiana BotaniGard strain against T. macfarlanei is reported as promising and suitable for managing this pest (Tahmina et al. 2020). For the appropriate management of spider mites, the interest in mycoacaricides has increased in recent years, especially B. bassiana is proven trustworthy (Alves et al. 2002, 2005; Shi & Feng 2006, 2009; Seiedy et al. 2010). However, the effectiveness of entomopathogenic fungi is regulated by several abiotic factors such as temperature, humidity, and solar radiation (Benz 1987; Inglis et al. 2001; Alves et al. 2005; Seiedy et al. 2010), host population level, and the presence of antagonists (James et al. 2003; Toledo et al. 2011). Some studies have shown that the temperature, humidity, UV radiation, etc., separately causes a reduction in the viability and virulence of the conidia after application, resulting in poor performance by the entomopathogenic fungi (Zimmermann 2007). Successful use of mycoinsecticides relies particularly on ambient relative humidity (RH) conditions and the concentration of conidia applied (Ferron et al. 1991; Alves et al. 2005; Devi & Rao 2006). The development of an efficient management strategy for controlling spider mites by using a particular B. bassiana strain requires a proper combination of both the conidial concentration and relative humidity conditions. Therefore, this study was designed to determine the effect of relative humidity on the efficacy of B. bassiana against T. macfarlanei.

Materials and methods

Collection and rearing of Tetranychus macfarlanei

The mite strain of T. macfarlanei was collected from a brinjal plant (Solanum melongena L.) (Solanaceae) in Dhaka, Bangladesh (23°82′N, 90°38′E) on 27 March 2020. They were maintained on bean (Dolichos lablab L.) leaves (ca. 25 cm2) kept in contact with water-saturated polyurethane mats in plastic Petri dishes (90-mm diameter, 20-mm depth) at 25 ± 1 °C, 65 ± 5% relative humidity, and 16L: 8D h photoperiod. The edges of the bean leaves were covered with moist tissue paper through watering and prevented mites from escaping. The leaves were replaced when they were exploited by the feeding of spider mites (Ullah et al. 2014).

Fungal pathogen and preparation of conidial suspension

A commercially available entomopathogenic fungus, B. bassiana, strain GHA contained 1.6×1010 fungal conidia/ml (BotaniGard® ES; Arysta LifeScience, Tokyo, Japan) was used in the bioassay tests. Suspension was prepared by diluting of formulated mycopesticide BotaniGard containing strain GHA of B. bassiana at concentration 1.6×1010 conidia/ml. Conidial suspensions were vortexed for 5 min, and spore concentrations were determined using a haemocytometer (Neubauer-improved haemocytometer, Lauda-Königshofen, Germany). The viability of conidia was determined before the bioassay by spread-plating 0.1 ml of conidial suspension titrated to 1×104 conidia ml-1 on SDA plates. Plates were incubated at 25 ± 1 °C, and the percentage germination was determined after 24 h from 100-spore counts by placing a sterile microscope coverslip on each plate under a stereomicroscope (SZ40, Olympus Corporation, Tokyo, Japan) (Ullah & Lim 2017). Each plate was replicated 4 times. Conidia germination > 90% was observed in all tests. The commercial bottle was shaken properly and the conidial suspensions, 1×108 conidia/ml, 1×107 conidia/ml, and 1×106 conidia/ml were prepared using distilled water.

Achieving different relative humidity (RH) regimes

Three different RH regimes, 55, 75, and 95 ± 2% achieved by dissolving Mg (NO3)26H2O, NaCl, and K2SO4 in distilled water were used in the experiments, respectively (Rockland 1960). Salt solutions were dissolved in water in a beaker, and the mixture was placed on a magnetic heating stirrer. The solution was allowed to cool and then poured down into desiccators. The RH was measured using a data logger (Thermometer and Hygrometer, SKU KUT527, Daiso, Japan).

Effects of Beauveria bassiana BotaniGard strain against T. macfarlanei eggs under different humidity

The three to 5-day-old gravid females of T. macfarlanei were transferred on bean leaf discs (ca. 16 cm2) placed with their lower side up in contact with water-saturated polyurethane mats in plastic Petri dishes (9 cm diameter). The spider mites were allowed to lay eggs for 24 h at 25°C, 60–70% RH, and a 16:8 h L: D photoperiod. Then the females were removed, and eggs were counted on each leaf disc. Subsequently, the test units were sprayed with the three concentrations (1×106, 1×107, and 1×108 conidia/ml) of B. bassiana (1 ml/cm2) by using a hand sprayer (52G-20CM-IMP, RFL best buy, Bangladesh). After air drying, the leaf discs with eggs were kept under three RH regimes (55, 75, and 95 ± 2%), all at 25 ± 1°C, and a 16:8 h L: D photoperiod. Mortality was recorded 144 h following the application, and eggs that did not hatch were scored as “dead”. The duration of the egg stage until larval hatching is less than 130 h for T. macfarlanei (Ullah et al. 2012). A total of 342–374 eggs obtained from 20 females were used for each humidity. A group of test units sprayed using distilled water served as the control.

Effects of Beauveria bassiana BotaniGard strain against T. macfarlanei adult females under different humidity

Three to 5-day-old gravid females of T. macfarlanei were transferred on bean leaf disc (ca. 16 cm2) placed in plastic Petri dishes as described earlier. The test units were incubated for 24 h. Dead or injured individuals were then removed, and the test units were sprayed with the three concentrations described above. After air drying, the mite-infested discs were kept under three RH regimes (55, 75, and 95 ± 2%), all at 25±1°C and a 16:8 h L: D photoperiod in an incubator until the mites' death. Mites that did not move their appendages when touched with a fine brush were considered dead, and mortality was recorded. Four replicates, each with 20 individuals for each fungal concentration and humidity regime, were used in the experiments. A group of test units sprayed using distilled water served as the control.

Data analysis

The percentages of dead eggs and adult females were corrected using the formula suggested by Abbott (1925):

Corrected mortality (%) = [100×(Treated – Control) /(100 – Control)]

The LT50 and LT90 were determined by Probit analysis using POLO-Plus (LeOra software). The correction of overlapping confidence intervals of the LT50 was used to establish whether lines were significantly different at the 5% level (Robertson et al. 2007). Before analysis, the values (egg) were arcsine transformed to normalize the data. A test for significant variation in the mean egg mortality was performed to reveal interactions between humidity and concentration factors by two-way analysis of variance (IBM 2019).


Effect of relative humidity on the efficacy of Beauveria bassiana against eggs of Tetranychus macfarlanei

Humidity and concentrations of B. bassiana significantly affect the mortality of T. macfarlanei eggs (humidity F=23.85, df=2, 27, P < 0.001; concentration F=31.10, df=2, 27, P < 0.001), but their interaction was not significant (humidity×concentration F=1.57, df=2, 27, P=0.210). The egg mortality was significantly higher at 95 and 75% RHs than at 55% RH at the same concentration (Fig. 1). The mortality in control was ≤ 5% in all concentrations. The corrected egg mortality was 91, 86.4, and 72% at 95, 75, and 55% RHs, respectively, with the same conidial concentration of 1×108 conidia/ml. The egg mortality increased with the increasing conidial concentration from 1×106 to 1×108 conidia/ml at the same RH condition. Mortality greatly increased with increasing RH only at the highest conidial concentration of B. bassiana.

Effect of relative humidity on the efficacy of Beauveria bassiana against adult females of Tetranychus macfarlanei

Adult mortality greatly increased with increasing RH and at a higher conidial concentration of B. bassiana. At 95% RH, the LT50 values were 28.7, 48.6, and 76.1 h at 1×108, 1×107, and 1×106 conidia/mL, respectively, which was not significantly different at 75% RH when compared with the same conidial concentrations of B. bassiana (33.4, 51.9, and 79.9 h, respectively; Table 1). At 55% RH, the LT50 values were 52.6, 91.4, and 130.1 h at the respective conidia/ml, which was significantly higher than other RHs despite the individual concentrations. The LT90 values at different RHs also showed a similar trend to LT50.


Corrected egg mortality of Tetranychus macfarlanei exposed to different concentrations of Beauveria bassiana at 95, 75 and 55% relative humidity conditions at 25 ± 1°C. Error bars indicate 95% confidence intervals.


Relative humidity at different conidial concentrations has a significant impact on the survivorship of adult females. The survivorship of adult females was decreased with increasing RH along with higher conidial concentrations. The survival was higher in lower conidial concentrations recorded at 17 days, 12 days and 8 days at 1×106, 1×107, and 1×108 conidia/ml, respectively, with the same RH of 95 ± 2% (Fig. 2). The LT50 of adult female survival was also decreased as conidial concentrations increased at 75% RH (79.4, 51.9 and 33.4 h at 1×106, 1×107, and 1×108 conidia/ml, respectively) and 55% RH (130.1, 91.4, and 52.6 h at 1×106, 1×107, and 1×108 conidia/ml, respectively).


Susceptibility of adult females of Tetranychus macfarlanei to Beauveria bassiana at different relative humidity levels.



Survivorship of adult females of Tetranychus macfarlanei exposed to different concentrations of Beauveria bassiana at 95, 75, and 55% relative humidity conditions at 25 ± 1°C.



The experiments were conducted to evaluate the effect of relative humidity on the efficacy of the fungal pathogen B. bassiana against the spider mite, T. macfarlanei. The effect was observed on the egg and adult mortalities of the spider mite by creating different humidity conditions under laboratory conditions. The results revealed that humidity had a positive effect on efficacy of mycopesticide. The best result was obtained at a concentration of 1×108 conidia/ml under 75 to 95% relative humidity conditions.

Several studies have also revealed the effect of B. bassiana against spider mites, including T. macfarlanei, at different concentrations. The response of adult female T. macfarlanei was dependent on the concentration of B. bassiana; the LC50 and LC90 values were 3.63×107 and 2.68×108 conidia/ml, respectively (Tahmina et al. 2020). B. bassiana was reported as highly effective against the eggs of Tetranychus urticae Koch under laboratory conditions (Basak et al. 2021). Beauvericin, a B. bassiana mycotoxin, was reported to cause 100% mortality on motile stages of T. urticae at a concentration of both 100 and 1000µg/g, while inhibited egg hatching up to 69.3 and 83.3%, respectively (Al Khoury et al. 2019). B. bassiana MK918495 isolate caused 27.6 to 89.2% mortality in T. urticae 7 days after treatment at varying concentrations ranging from 4×104 to 4×109 conidia/ml (Athisintha et al. 2019). B. bassiana isolate B2 was reported to be effective against T. urticae as it caused 70, 80, and 84% mortality at 105, 106 and 107 conidia/ml concentrations, respectively (Ahmad et al. 2018). Among 12 isolates of B. bassiana applied in a study against T. urticae, SCWJ2, SDDZ-9, LNSZ-26, GZGY-1-3, and WLMQ-32 strains were reported as the most potent; they caused 37.6–49.5% corrected adult mortality at a concentration of 1×107 conidia/ml after 4 days following the treatment (Wu et al. 2016). The susceptibility of different developmental stages of T. urticae to the entomopathogenic fungi B. bassiana was evaluated under laboratory conditions. The study revealed that the highest conidial concentration (1×107 conidia/ml) significantly reduced the viability of eggs and increased the mortality of motile stages (Bugeme et al. 2014). B. bassiana Naturalis-L reduced around 97% of T. urticae population in a tomato greenhouse when applied at a rate of 1×108 conidia/ml (Chandler et al. 2005). It has been reported that B. bassiana has the potential to suppress future generations of Tetranychus ludeni Zacher by reducing its oviposition rate (Pereira et al. 2019).

The effectiveness of B. bassiana against spider mites in some studies showed poor performance. Some isolates of B. bassiana having 1×107 conidia/ml concentration showed poor performance against the eggs, immatures, and adults of T. urticae where laboratory bioassays showed their corrected mortalities were 2.7–3.8, 17.5–25.8, and 63.2–71.2%, respectively (Wu et al. 2019). A relatively higher concentration of 1×108 conidia/ml, B. bassiana 432.99 and Naturalis-L isolates caused lower rates of mortality of T. urticae under laboratory conditions, and the mortality recorded were 46.2–72.2% and 52.1–95.2%, respectively (Chandler et al. 2005). B. bassiana isolate 447 was found ineffective against T. urticae in a laboratory assay. Even at a higher concentration of 1×109 conidia/ml and 70±5% RH, only 51.7% mortality occurred (Andreleva & Shternshis 1995; Tamai et al. 1999). Other isolates of B. bassiana showed poor performance against T. urticae; when used at the rate of 1×107 conidia/ml, it causes 16–33% mortality following six days after inoculation (Chandler et al. 2005). A series of factors such as experimental condition, host type, application interval, temperature, humidity, rainfall, etc., plays a vital role in the virulence of the B. bassiana, and they may be responsible for this variation in the efficiency of the entomopathogen. The DNA characteristics and enzymatic activity of B. bassiana also significantly impact the outcome (Almeida et al. 1997; Moino et al. 1998).

In the case of spider mites, the effect of relative humidity on the efficacy of B. bassiana was reported in some experiments. A laboratory bioassay of B. bassiana against T. urticae on leaf discs and potted bean plants revealed that the LT50 value was significantly lower at 1×108 conidia/ml and 95% RH than values for other lower RH levels at the same conidial concentration. A 1×107 conidia/ml concentration followed a similar trend (Ullah & Lim 2015). In the greenhouse, B. bassiana causes a higher percentage of infection (60–88.8%) to mites and insects under 97.5% RH, while at 75 and 80% RH only 15.3–43.9% of them were infected. A fifteen percent increase in RH results into 17–25% increase in the percentage of infection (Shipp et al. 2003). The 35% increase in the humidity level caused 8–12% increase in the mortality for B. bassiana AT076 on the 3rd and 5th days after application, respectively (Ortucu & Algur 2017).

Our results showed that infection of T. macfarlanei by B. bassiana was highly dependent on the conidial concentrations and the RH conditions. But a conidial concentration lower than 1×108 conidia/ml caused lower mortality irrespective of RH values. The test mites are small, and their cryptic living works (silky thread) are a barrier to efficient use of the applied concentration. As a result, there might be less possibility of contact in concentration below the threshold. The mites' defense mechanism triggers phagocytosis, melanization, or encapsulation responses as soon as harmful foreign molecule enters. So, if a lower number of conidia encounters the insect cuticle, it gets easier for the mites' immune system to combat them. No infection is thus apparent when the conidial dose is lower than the threshold (Devi & Rao 2006). It has been reported that a certain amount of pathogen concentration is required for successful infection, such as 1×107 conidia/ml B. bassiana against Metarhizium anisopliae (Metschnikoff) Sorokin (Coleoptera: Meloidae) (Devi & Rao 2006), 1.6×108 conidia/m2 of M. anisopliae (Ascomycota: Hypocreales) against Anopheles gambiae Giles and Culex quinquefasciatus Say (Diptera: Culicidae) (Scholte et al. 2003), and 1×106 conidia/ml of M. anisopliae isolate Qu-M984 against Pseudococcus viburni (Signoret) (Hemiptera: Pseudococcidae) (Pereira et al. 2011). Moreover, higher concentrations of B. bassiana are known to infect Lygus hesperus Knight (Hemiptera: Miridae) even at lower humidity (Dunn & Mechalas 1963). Viable fungal conidium is a prerequisite for germination and infection. Germination percentage in vitro determines fungal virulence (Altre et al. 1999). The conidial germination largely depends on RH and temperature (Feng et al. 1994; Roberts & St. Leger 2004), and spider mite eggs are usually laid on the surfaces of leaves with some moisture (e.g., metabolic water, dew). The high egg mortalities caused by B. bassiana at the same regimes may be interpreted as the effect of egg moisture or humidity that facilitated germination and increased the virulence of the entomopathogen B. bassiana. This indicates that the emulsifiable formulation would be an effective choice for the use of B. bassiana against spider mites under field conditions. The results of the current study indicated that infection of T. macfarlanei eggs and adults caused by B. bassiana was highly dependent on relative humidity and conidial concentration. The leaf disc assay showed that a concentration of B. bassiana of 1×108 and a RH of 95 ± 2% was very effective for managing T. macfarlanei. The LT50 and LT90 values were 28.7 h and 71.69 h, respectively. This period was significantly shorter than those for lower RHs with the same conidial concentration. Both egg and adult mortality were higher at 95 ± 2% RH than at lower RHs, irrespective of conidial concentrations. It showed that an increasing RH value increases the efficacy of fungal entomopathogen. The best result was obtained when RH was higher, and the concentration was at the threshold level.

Finally, it can be concluded that the efficacy of the entomopathogen B. bassiana increases with raising of humidity. Beauveria bassiana is a promising alternative for the successful management of T. macfarlanei in IPM programmes. So, this study will contribute to developing an appropriate pest management strategy for spider mites using an entomopathogenic fungus considering humidity conditions. However, the field application of B. bassiana needs to be accurately evaluated for its effectiveness.


We acknowledge the University Grants Commission of Bangladesh for funding and Bangladesh Agricultural University Research System (BAURES) for their management. Md. Nahian-Al Sabri received National Science and Technology Fellowship from the Ministry of Science and Technology, Government of Bangladesh, to conduct this research.

Conflict of interest

The authors have no conflict of interest to declare.



Abbott, W.S. (1925) A method of computing the effectiveness of an insecticide. Journal of Economic Entomology , 18(2), 265–267.  Google Scholar


Ahmad, M., Ghaza, I., Kerhili, S. & Rajab, L. (2018) The pathogenicity of the fungus Beauveria bassiana (Bals.) Vuil. on adults and eggs of the two spotted spider mite Tetranychus urticae Koch in the laboratory. Arab Journal of Plant Protection , 36(3), 199–206.  Google Scholar


Al Khoury, C., Guillot, J. & Nemer, N. (2019) Lethal activity of beauvericin, a Beauveria bassiana mycotoxin, against the two-spotted spider mites, Tetranychus urticae Koch. Journal of Applied Entomology , 143(9), 974–983.  Google Scholar


Al Khoury, C., Guillot, J. & Nemer, N. (2020) Susceptibility and development of resistance of the mite Tetranychus urticae to aerial conidia and blastospores of the entomopathogenic fungus Beauveria bassiana. Systematic & Applied Acarology , 25(3), 429–443.  Google Scholar


Almeida, J.D., Alves, S.B. & Pereira, R.M. (1997) Selection of Beauveria spp. isolates for control of the termite Heterotermes tenuis (Hagen, 1858). Journal of Applied Entomology , 121(1–5), 539–543.  Google Scholar


Altre, J.A., Vandenberg, J.D. & Cantone, F.A. (1999) Pathogenicity of Paecilomyces fumosoroseus isolates to diamondback moth, Plutella xylostella: correlation with spore size, germination speed, and attachment to cuticle. Journal of Invertebrate Pathology , 73(3), 332–338.  Google Scholar


Alves, S.B., Rossi, L.S., Lopes, R.B., Tamai, M.A. & Pereira, R.M. (2002) Beauveria bassiana yeast phase on agar medium and its pathogenicity against Diatraea saccharalis (Lepidoptera: Crambidae) and Tetranychus urticae (Acari: Tetranychidae). Journal of Invertebrate Pathology , 81(2), 70–77.  Google Scholar


Alves, S.B., Tamai, M.A., Rossi, L.S. & Castiglioni, E. (2005) Beauveria bassiana pathogenicity to the citrus rust mite Phyllocoptruta oleivora. Experimental and Applied Acarology , 37(1–2), 117–122.  Google Scholar


Andreleva, I.V. & Shternshis, M.V. (1995) Microbiological formulations against web mites in greenhouses. Zashchita Rasteniĭ Moskva , 41–42. (In Russian) Google Scholar


Athisintha, S., Manimegalai, S., Vishnupriya, R., Muthulakshmi, P. & Nithya, P.R. (2019) Infection process and pathogenicity of Beauveria bassiana (Balsamo) Vuillemin against Tetranychus urticae Koch. Annals of Plant Protection Sciences , 27(2), 194–199.  Google Scholar


Basak, R., Akter, M., Tumpa, T.A., Sharmin, D. & Ullah, M.S. (2021) Laboratory bioassay of six pesticides, an entomopathogenic fungus, and a botanical pesticide on two-spotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae). Persian Journal of Acarology , 10(3), 269–280. Google Scholar


Benz, G. (1987) Environment. In : Fuxa, J.R. & Tanada, Y. (Eds.), Epizootiology of Insect Diseases. New York: John Wiley and Sons, pp. 177–214. Google Scholar


Bolland, H.R., Gutierrez, J. & Flechtmann, C.H.W. (1998) World Catalogue of the Spider Mite Family (Acari:Tetranychidae). Leiden, Brill, 392 pp. Google Scholar


Bugeme, D., Knapp, M., Boga, H., Ekesi, S. & Maniania, N. (2014) Susceptibility of developmental stages of Tetranychus urticae (Acari: Tetranychidae) to infection by Beauveria bassiana and Metarhizium anisopliae (Hypocreales: Clavicipitaceae). International Journal of Tropical Insect Science , 34(3), 190–196. Google Scholar


Chandler, D., Davidson, G., Pell, J.K., Ball, B.V., Shaw, K. & Sunderland, K.D. (2000) Fungal biocontrol of Acari. Biocontrol Science and Technology , 10(4), 357–384.  Google Scholar


Chandler, D., Davidson, G. & Jacobson, R.J. (2005) Laboratory and glasshouse evaluation of entomopathogenic fungi against the two-spotted spider mite, Tetranychus urticae (Acari: Tetranychidae), on tomato, Lycopersicon esculentum. Biocontrol Science and Technology , 15(1), 37–54.  Google Scholar


Chen, X., Li, L., Hu, Q., Zhang, B., Wu, W., Jin, F. & Jiang, J. (2015) Expression of dsRNA in recombinant Isaria fumosorosea strain targets the TLR7 gene in Bemisia tabaci. BMC Biotechnology , 15(1), 1–8.  Google Scholar


Devi, K.U. & Rao, C.U. (2006) Allee effect in the infection dynamics of the entomopathogenic fungus Beauveria bassiana (bals) Vuill. on the beetle, Mylabris pustulata. Mycopathologia , 161(6), 385–394.  Google Scholar


Dunn, P.H. & Mechalas, B.J. (1963) Potential of Beauveria bassiana (Balsamo) Vuillemin as a microbial insecticide. Journal of Invertebrate Pathology , 5(4), 451–459. Google Scholar


Faria, M. & Wraight, S. (2001) Biological control of Bemisia tabaci with fungi. Crop Protection , 20, 767–778.  Google Scholar


Feng, M.G., Chen, B. & Ying, S.H. (2004) Trials of Beauveria bassiana, Paecilomyces fumosoroseus and imidacloprid for management of Trialeurodes vaporariorum (Homoptera: Aleyrodidae) on greenhouse grown lettuce. Biocontrol Science and Technology , 14(6), 531–544.  Google Scholar


Feng, M.G., Poprawski, T.J. & Khachatourians, G.G. (1994) Production, formulation and application of the entomopathogenic fungus Beauveria bassiana for insect control: current status. Biocontrol Science and Technology , 4(1), 3–34.  Google Scholar


Ferron, P., Fargues, J. & Riba, G. (1991) Fungi as microbial insecticides against pests. In : Arora, D.K., Ajello, L. & Mukerji K.G. (Eds.), Handbook of Applied Mycology: Humans, Animals and Insects (Vol. 2). Marcel Dekker, New York, pp. 665–706. Google Scholar


Groden, E., Wraight, S.P. & Drummond, F.A. (2002) Microbial control of colorado potato beetle in rain-fed potato agroecosystems in the northeastern US. Proceedings of the International Colloqium on Invertebrate Pathology and Microbial Control , 8, 265–269. Google Scholar


Hatting, J.L., Wraight, S.P. & Miller, R.M. (2004) Efficacy of Beauveria bassiana (Hyphomycetes) for control of Russian wheat aphid (Homoptera: Aphididae) on resistant wheat under field conditions. Biocontrol Science and Technology , 14(5), 459–473.  Google Scholar


IBM. (2019) IBM SPSS Statistics for Windows, Version 26.0. Armonk, NY, IBM Corp. Google Scholar


Inglis, D.G., Goettel, S.M., Butt, M.T. & Strasser, H. (2001) Use of hyphomycetes fungi for managing insect pests. In : Butt, T.M., Jackson, C. & Magan, N. (Eds.), Fungi as Biocontrol Agents. Wallingford, CABI Publishing, pp. 23–27. Google Scholar


James, R.R., Buckner, J.S. & Freeman, T.P. (2003) Cuticular lipids and silverleaf whitefly stage affect conidial germination of Beauveria bassiana and Paecilomyces fumosoroseus. Journal of Invertebrate Pathology , 84(2), 67–74.  Google Scholar


Jeppson, L.R., Keifer, H.H. & Baker, E.W. (1975) Mites Injurious to Economic Plants. Berkeley, California USA, University of California Press, 614 pp. Google Scholar


Khachatourians, G.G. & Qazi, S.S. (2008) Entomopathogenic fungi: biochemistry and molecular biology. In : Howard, D.H. & Miller, J.D. (Eds.), Human and Animal Relationships. Berlin, Heidelberg, Springer, pp. 33–61.  Google Scholar


Lacey, L.A., Grzywacz, D., Shapiro-Ilan, D.I., Frutos, R., Brownbridge, M. & Goettel, M.S. (2015) Insect pathogens as biological control agents: Back to the future. Journal of Invertebrate Pathology , 132, 1–41.  Google Scholar


Li, S.J., Xue, X., Ahmed, M.Z., Ren, S.X., Du, Y.Z., Wu, J.H., Cuthbertson, G.L. & Qiu, B.L. (2011) Host plants and natural enemies of Bemisia tabaci (Hemiptera: Aleyrodidae) in China. Insect Science , 18(1), 101–120.  Google Scholar


Migeon, A. & Dorkeld, F. (2022) Spider Mites Web: a comprehensive database for the Tetranychidae. Available from 14 March 2022). Google Scholar


Moino Jr, A., Alves, S.B. & Pereira, R.M. (1998) Efficacy of Beauveria bassiana (Balsamo) Vuillemin isolates for control of stored-grain pests. Journal of Applied Entomology , 122(1–5), 301–305.  Google Scholar


Mota-Sanchez, D. & Wise, J.C. (2022) Arthropod pesticide resistance database [Internet]. Available from 2022 March 6). Google Scholar


Ortucu, S. & Algur, O.F. (2017) A laboratory assessment of two local strains of the Beauveria bassiana (Bals.) Vuill. against the Tetranychus urticae (Acari: Tetranychidae) and their potential as a mycopesticide. Journal of Pathogens , 7628175.  Google Scholar


Pereira, A., Casals, P., Salazar, A.M. & Gerding, M. (2011) Virulence and pre-lethal reproductive effects of Metarhizium anisopliae var. anisopliae on Pseudococcus viburni (Hemiptera: Pseudococcidae). Chilean Journal of Agricultural Research , 71(4), 554–559.  Google Scholar


Pereira, S.L., Reis, T.C., de Oliveira, I.T., Ferreira, E.A., de Castro e Castro, B.M., Soares, M.A. & Vidal Ribeiro, V.H. (2019) Pathogenicity of Metarhizium anisopliae and Beauveria bassiana fungi to Tetranychus ludeni (Acari: Tetranychidae). Arquivos do Instituto Biológico , 86, 1–7, e0272018.  Google Scholar


Pu, X., Feng, M. & Shi, C. (2005) Impact of three application methods on the field efficacy of a Beauveria bassiana-based mycoinsecticide against the false-eye leafhopper, Empoasca vitis (Homoptera: Cicadellidae) in the tea canopy. Crop Protection , 24, 167–175.  Google Scholar


Roberts, D.W. & St Leger, R.J. (2004) Metarhizium spp., cosmopolitan insect-pathogenic fungi: mycological aspects. Advances in Applied Microbiology , 54, 1–70.  Google Scholar


Robertson, J.L., Savin, N.E., Savin, N.E. & Preisler, H.K. (2007) Bioassays with Arthropods (2nd edition). CRC Press, 224 pp. Google Scholar


Rockland, L.B. (1960) Saturated salt solutions for static control of relative humidity between 5° and 40°C. Analytical Chemistry , 32(10), 1375–1376.  Google Scholar


Scholte, E.J., Njiru, B.N., Smallegange, R.C., Takken, W. & Knols, B.G. (2003) Infection of malaria (Anopheles gambiae ss) and filariasis (Culex quinquefasciatus) vectors with the entomopathogenic fungus Metarhizium anisopliae. Malaria Journal , 2(1), 1–8. Google Scholar


Seiedy, M., Saboori, A., Allahyari, H., Talaei-Hassanloui, R. & Tork, M. (2010) Laboratory investigation on the virulence of two isolates of the entomopathogenic fungus Beauveria bassiana against the twospotted spider mite Tetranychus urticae (Acari: Tetranychidae). International Journal of Acarology , 36(6), 527–532.  Google Scholar


Shi, W.B. & Feng, M.G. (2006) Field efficacy of application of Beauveria bassiana formulation and low rate pyridaben for sustainable control of citrus red mite Panonychus citri (Acari: Tetranychidae) in orchards. Biological Control , 39(2), 210–217.  Google Scholar


Shi, W.B. & Feng, M.G. (2009) Effect of fungal infection on reproductive potential and survival time of Tetranychus urticae (Acari: Tetranychidae). Experimental and Applied Acarology , 48(3), 229–237.  Google Scholar


Shipp, J.L., Zhang, Y., Hunt, D.W.A. & Ferguson, G. (2003) Influence of humidity and greenhouse microclimate on the efficacy of Beauveria bassiana (Balsamo) for control of greenhouse arthropod pests. Environmental Entomology , 32(5), 1154–1163.  Google Scholar


Tahmina, M., Basak, R., Arafat, Y., Sharmin, D., Jahan, M. & Ullah, M.S. (2020) Comparative efficacy of chemicals, entomopathogenic fungus and botanical for the management of red spider mite Tetranychus macfarlanei. Journal of South Pacific Agriculture , 23, 1–7. Google Scholar


Tamai, M.A., Alves, S.B., Almeida, J.D. & Faion, M. (2002) Avaliação de fungos entomopatogênicos para o controle de Tetranychus urticae Koch (Acari: Tetranychidae). Arquivos do Instituto Biológico , 69(3), 7–84. Google Scholar


Tamai, M.A., Alves, S.B. & Neves, P.J. (1999) Pathogenicity of Beauveria bassiana (Bals.) Vuill. against Tetranychus urticae Koch. Scientia Agricola , 56, 285–288.  Google Scholar


Toledo, A.V., Alippi, A.M. & de Remes Lenicov, A.M.M. (2011) Growth inhibition of Beauveria bassiana by bacteria isolated from the cuticular surface of the corn leafhopper, Dalbulus maidis and the planthopper, Delphacodes kuscheli, two important vectors of maize pathogens. Journal of Insect Science , 11(1), 29.  Google Scholar


Ullah, M.S. & Gotoh, T. (2013) Laboratory-based toxicity of some acaricides to Tetranychus macfarlanei and Tetranychus truncatus (Acari: Tetranychidae). International Journal of Acarology , 39(3), 244–251.  Google Scholar


Ullah, M.S. & Lim, U.T. (2015) Laboratory bioassay of Beauveria bassiana against Tetranychus urticae (Acari: Tetranychidae) on leaf discs and potted bean plants. Experimental and Applied Acarology , 65(3), 307–318.  Google Scholar


Ullah, M.S. & Lim, U.T. (2017) Laboratory evaluation of the effect of Beauveria bassiana on the predatory mite Phytoseiulus persimilis (Acari: Phytoseiidae). Journal of Invertebrate Pathology , 148, 102–109.  Google Scholar


Ullah, M.S., Gotoh, T. & Lim, U.T. (2014) Life history parameters of the phytophagous spider mites, Tetranychus piercei, T. truncatus and T. bambusae (Acari: Tetranychidae). Journal of Asia-Pacific Entomology , 17, 767–773.  Google Scholar


Ullah, M.S., Haque, M.A., Nachman, G. & Gotoh, T. (2012) Temperature dependent development and reproductive traits of Tetranychus macfarlanei (Acari: Tetranychidae). Experimental and Applied Acarology , 56, 327–344.  Google Scholar


Ullah, M.S., Hossain, M.A., Jahan, M., Sarker, M.A. & Hamim, I. (2021) A Field Guide of Major Insect Pests and Diseases of Different Crops in Bangladesh. Bangladesh Agricultural University Extension Centre (BAUEC), 500 pp. Google Scholar


Van Leeuwen, T., Vontas, J., Tsagkarakou, A. & Tirry, L. (2009) Mechanisms of acaricide resistance in the two-spotted spider mite Tetranychus urticae. In : Ishaaya, I. & Horowitz, A.R. (Eds.), Biorational Control of Arthropod Pests. Dordrecht, Springer, pp. 347–393. Google Scholar


Whalon, M.E., Mota-Sanchez, D., Hollingworth, R.M. & Duynslager, L. (2021) Arthropod pesticide resistance database [Internet]. Available from 2022 March 6). Google Scholar


Wu, S., Sarkar, S.C., Lv, J., Xu, X. & Lei, Z. (2019) Poor infectivity of Beauveria bassiana to eggs and immatures causes the failure of suppression on Tetranychus urticae population. BioControl , 65(1), 81–90.  Google Scholar


Wu, S., Xie, H., Li, M., Xu, X. & Lei, Z. (2016) Highly virulent Beauveria bassiana strains against the twospotted spider mite, Tetranychus urticae, show no pathogenicity against five phytoseiid mite species. Experimental and Applied Acarology , 70(4), 421–435.  Google Scholar


Zimmermann, G. (2007) Review on safety of the entomopathogenic fungi Beauveria bassiana and Beauveria brongniartii. Biocontrol Science and Technology , 17, 553–596.  Google Scholar
MD. Nahian-Al Sabri, Mahbuba Jahan, Tetsuo Gotoh, İsmail Döker, and Mohammad Shaef Ullah "Effect of relative humidity on the efficacy of entomopathogen Beauveria bassiana-based mycopesticide against red spider mite Tetranychus macfarlanei," Systematic and Applied Acarology 27(12), 2414-2425, (28 November 2022).
Received: 8 April 2022; Accepted: 29 September 2022; Published: 28 November 2022

abiotic factors
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