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Review

Insecticide Resistance and Its Management in Two Invasive Cryptic Species of Bemisia tabaci in China

by
Qian Wang
,
Chen Luo
* and
Ran Wang
*
Institute of Plant Protection, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(7), 6048; https://doi.org/10.3390/ijms24076048
Submission received: 14 January 2023 / Revised: 12 March 2023 / Accepted: 13 March 2023 / Published: 23 March 2023
(This article belongs to the Special Issue Natural and Synthetic Toxins: Molecular Aspects and Development Treatment Strategy II)
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Abstract

:
The sweet potato whitefly Bemisia tabaci is a major agricultural pest with a wide host range throughout the world. The species designation for B. tabaci includes numerous distinct cryptic species or biotypes. Two invasive B. tabaci biotypes, MEAM1 (B) and MED (Q), were found in China at the end of the 20th century and at the beginning of the 21st century. MEAM1 (B) and MED (Q) show higher pesticide resistance levels than native strains, and the levels of resistance vary with changes in insecticide selection pressure. Recent studies have revealed metabolic resistance mechanisms and target site mutations in invasive B. tabaci strains that render them resistant to a range of insecticides and have uncovered the frequency of these resistance-related mutations in B. tabaci populations in China. Novel pest control agents, such as RNA-based pesticides and nano-pesticides, have achieved effective control effects in the laboratory and are expected to be applied for field control of B. tabaci in the future. In this review, we discuss the mechanisms of resistance developed by these invasive B. tabaci populations since their invasion into China. We also provide suggestions for ecologically sound and efficient B. tabaci control.

1. Introduction: The Whitefly Bemisia tabaci

The sweet potato whitefly B. tabaci is an insect pest that causes serious agricultural and economic losses throughout the world [1]. This pest damages host plants by feeding on phloem sap and secreting honeydew on leaves and fruits. It serves as a vector for more than 100 plant viruses, including causative agents of serious plant diseases, such as cotton leaf curl virus (CLCV), cassava mosaic disease (CMD), and cassava brown streak disease (CBSD). B. tabaci encompasses numerous distinct cryptic species or biotypes; biotypes B (Middle East Asia Minor 1 [MEAM1]) and Q (Mediterranean [MED]) are by far the most widespread [2].
B. tabaci has been recorded as causing damage in China since 1949 [3], but increasingly serious damage has occurred since the beginning of the 21st century. A sudden outbreak of B. tabaci in China attracted the attention of researchers, and the populations involved were identified in 2002 as the biotype MEAM1 (B). This identification was accomplished by sequencing a fragment of the mitochondrial cytochrome oxidase I gene (mtCOI) [4]. From the time of invasion to the determination of the relevant biotype, MEAM1 (B) rapidly spread to more than ten provinces in China and caused serious damage to a variety of vegetables, flowers, garden plants, and cash crops. MEAM1 (B) showed the ability to outcompete and replace non-B populations over a short period of time.
At the beginning of the 21st century, MED (Q) was first detected in Henan Province and Beijing using the same mtCOI sequencing method [5]. Since then, MED (Q) has been continually reported in different regions of China, rapidly displacing MEAM1 (B) in most locations [6]. Field biotype investigations revealed that the proportion of MED (Q) individuals in China increased tremendously from 2003 to 2014 [7]. Most field-collected populations from different cities and regions in 2011 were identified as MED (Q), but the populations in several areas were of mixed Q and B biotypes [8]. In 2018, MED (Q) was distributed across all areas of Xinjiang [9]. By 2020, MED (Q) was the predominant cryptic species in most areas of China [10].
This process involved two sequential rapid invasions of novel B. tabaci biotypes to replace local populations; MEAM1 (B) first displaced non-B populations over a short time period, then MED (Q) rapidly spread to almost all provinces and cities in China and established population dominance [8,11]. The competitive substitution between biotypes was considered to be related to several factors: fitness costs, insecticide resistance, viral vector capacity, and host plant adaptation range [12]. MEAM1 (B) has significant survival advantages compared to MED (Q), but it is often replaced by MED (Q) in the field. MED (Q) shows higher levels of resistance to insecticide than MEAM1 (B), indicating that the insecticide resistance advantage of MED (Q) can compensate for survival disadvantages in the field.

2. B. tabaci Resistance to Pesticides of Different Classes

The high level of pesticide resistance in invasive B. tabaci is considered as one of the important factors driving their rapid spread and replacement of native biotypes. Reported insect resistance mechanisms identified in B. tabaci populations in China are shown in Table 1. Single-nucleotide polymorphism (SNP) of cytochrome P450 monooxygenases (P450s) may cause an overexpression of P450-dependent monooxygenases, thus enhancing insecticide resistance [13]. However, the broad trends underlying the development of insecticide resistance and the specific resistance mechanisms used by invasive B. tabaci biotypes have remained largely unclear. Clarification of these points would allow the formulation of clear strategies to slow the development and spread of insecticide resistance and improve pesticide efficiency in the field. In Figure 1, we summarize the state of known insecticide resistance in invasive B. tabaci biotypes based on published reports from different locations throughout China.

2.1. Organophosphates (OPs) and Carbamates

Organophosphorus and carbamate insecticides were released in the 1950s. They are acetylcholinesterase inhibitors that have been applied for many years in China to control multiple pests. B. tabaci has developed a range of resistance levels to these pesticides [14]. In general, the development of insecticide resistance is closely associated with the amount and duration of insecticide application. Field MED (Q) populations in Fujian Province displayed high resistance to methamidophos and chlorpyrifos, which had been applied in the field for many years. However, in 2004, there was no apparent resistance of MED (Q) individuals in this area to phoxim, which had only been applied in the area since 2002 [15]. In 2006 and 2007, MEAM1 (B) and MED (Q) individuals in Guangzhou showed significantly higher resistance levels to acephate and methomyl than that of the local Cv population, which was collected in 2007 from the ornamental plant Codiaeum variegatum [16]. MED (Q) collected from eastern China in 2010 showed low resistance to dichlorvos and no resistance to carbosulfan, and the susceptible reference strain of B-biotype B. tabaci had high resistance; the median lethal concentrations (LC50 values) were 336 and 441 mg/L for dichlorvos and carbosulfan, respectively [14]. In comparison, these two pesticides still had high toxicities to field MED (Q) strains. Both MED (Q) and MEAM1 (B) individuals from China displayed extremely low sensitivity to chlorpyrifos [17,18]. However, China banned chlorpyrifos use on vegetables, and this insecticide has therefore not been in use in the field since 2016 [19]. Overall, MEAM1 (B) and MED (Q) have developed high resistance to most OPs and carbamate insecticides, but the resistance levels vary between populations and specific insecticides.
Target site insensitivity and detoxification enzyme activity are the major mechanisms by which B. tabaci exert resistance to OPs [14]. Esterase is the primary detoxification enzyme that participates in chlorpyrifos metabolism. A chlorpyrifos-resistant strain showed significantly higher esterase activity than a sensitive strain did, but there were no differences in acetylcholine esterase (AChE) activity [20]. An F392W mutation in Ace1, a point mutation in an ace1-type acetylcholinesterase, was shown to be responsible for OP resistance in B. tabaci in Israel [21]. However, this mutation was present in both chlorpyrifos-resistant and chlorpyrifos-susceptible strains from Nanjing and in six field-collected populations from elsewhere in China, indicating that carbamate insecticide resistance is widespread [20]. An investigation of another Ace1 mutation (F331W) that was associated with OP resistance revealed that all analyzed samples were homozygous for the mutation, indicating that the F331W mutation was fixed in wild whitefly populations across China [18].

2.2. Pyrethroids

Pyrethroid insecticides were released in the late 1960s. They were gradually but widely adopted due to their higher toxicity and lower required dosages compared to the older generation of organophosphorus insecticides. At the beginning of the MEAM1 (B) invasion into China, this biotype showed high resistance to pyrethroids, with resistance levels up to 1000-fold higher compared to the local populations [22]. Most invasive biotypes showed varying degrees of resistance to pyrethroids, with the exception of cypermethrin, to which MED (Q) populations from eastern China in 2010 were susceptible [14]. Both MEAM1 (B) and MED (Q) showed higher resistance to beta-cypermethrin than the native Cv population did [16]. By 2007–2008, both invasive biotypes from different regions of China were resistant to bifenthrin and cypermethrin, with no differences between the biotypes [23]. By 2019, most field populations in China had developed bifenthrin resistance [10]. Pyrethroid resistance generally functions through target site insensitivity or increased degradation activity of enzymes such as hydrolases and mixed-function oxidases (MFOs) [15]. Two specific point mutations in the gene encoding para-type voltage-gated sodium channel (VGSC), L925I and T929V, are associated with pyrethroid resistance in B. tabaci [24].

2.3. Insect Growth Regulators (IGRs)

Buprofezin and pyriproxyfen are IGRs that have long been used for B. tabaci control. Buprofezin is a chitin biosynthesis inhibitor, whereas pyriproxyfen is an analog of juvenile whitefly hormone. Invasive B. tabaci in China has developed a range of resistance levels to pyriproxyfen. MEAM1 (B) sampled from Xinjiang in 2004–2005 showed a pyriproxyfen resistance factor (RF) of 22–37 (LC50 = 0.022–0.037 mg/L), although this pesticide had not been in routine use in Chinese agriculture at that time [22]. Pyriproxyfen had an LC50 value of 1461 mg/L in lab-raised MEAM1 (B) adults descended from individuals collected in Beijing in 2000; the LC50 value was 8832 mg/L for lab-raised MED (Q) adults descended from individuals collected in Beijing in 2009, demonstrating a significant increase in resistance [25]. Furthermore, adults were significantly more pyriproxyfen-resistant than eggs and larvae in both populations, whereas eggs and adults showed significantly higher buprofezin resistance than larvae [25]. MED (Q) larvae collected from multiple Chinese provinces in 2013–2014 showed low to moderate levels of pyriproxyfen resistance, but the resistance levels markedly increased in 2014 [7]. From 2015 to 2018, MEAM1 (B) and MED (Q) individuals collected from regions throughout China showed low to high pyriproxyfen resistance, and resistance was dependent on developmental stage [19,26].

2.4. Neonicotinoids

Neonicotinoids have played a key role in B. tabaci control in the field for many years. This class of pesticides can be divided into four categories based on their chemical structure: chloronicotinyls, thianicotinyls, nitroguanidines, and sulfoximines (Figure 2). Neonicotinoids are nicotinic acetylcholine receptor (nAChR) competitive modulators, of which four generations have been released over time. At the beginning of the MEAM1 (B) invasion, this biotype showed moderate resistance to the first and second generations of neonicotinoid pesticides. The LC50 values for imidacloprid were five- to seven-fold higher in MEAM1 (B) and MED (Q) than in the local Cv populations [16]. In a lab-reared population of MEAM1 (B), thiamethoxam resistance developed slowly prior to the 17th generation and then rapidly increased. Thiamethoxam resistance in B. tabaci has high fitness costs, as demonstrated by the lower intrinsic rate of increase, gross reproductive rate, and net reproductive rate [27]. Field MED (Q) populations have consistently shown much higher resistance levels to imidacloprid, thiamethoxam, and acetamiprid than MEAM1 (B) populations [28]. In 2019, most MED (Q) populations in Xinjiang were susceptible to thiamethoxam, but were moderate to high resistant to imidacloprid [9]. MED (Q) from eastern China showed low to high resistance to the first- and second-generation neonicotinoids, but no resistance to third-generation neonicotinoids from 2013 to 2014 [29]. Flupyradifurone is a butenolide insecticide that has only been applied for a short time in China, but some field populations have already shown low to moderate levels of resistance; however, this resistance is associated with significant fitness costs [30].
Detoxification enzyme activity is a major mechanism of resistance to neonicotinoids. P450 monooxygenase plays a key role in the regulation of resistance; it shows significantly higher activity in neonicotinoid-resistant strains and is overexpressed in response to neonicotinoid stimulation [31,32]. Of the numerous P450 genes, several have been confirmed as being involved in the regulation of neonicotinoid resistance. These include cytochrome P450 (CYP) genes, such as CYP6CM1, CYP4C64, and CYP6CX4, and the glutathione-S-transferase (GST) s2 and d7 proteins (GSTs2 and GSTd7) [8,28,33,34,35,36]. CYP6CM1 expression levels are closely related to the resistance factors of B. tabaci populations to imidacloprid, thiamethoxam, acetamiprid, and pymetrozine [8,28]. CYP6CM1 is most closely associated with the regulation of imidacloprid resistance. A simulated binding model of CYP6CM1vQ with imidacloprid shows a relatively stable interaction, with two stable N-H···N H-bonds and a strong cation–π interaction between Arg225 and imidacloprid; in contrast, the interaction of CYP6CM1vQ with dinotefuran is weak [33]. Reducing CYP6CM1 mRNA levels is sufficient to decrease the resistance of an imidacloprid-tolerant strain to imidacloprid. The basic leucine zipper (bZIP) transcription factor, cAMP-response element-binding protein (CREB), directly regulates CYP6CM1 expression, and the extracellular signal-related kinase (ERK) and p38 mitogen-activated protein kinase (MAPK) signaling pathways activate CREB transcription [35]. The relative expression levels of CYP6CX4 and GSTs2 in a flupyradifurone-tolerant B. tabaci strain were markedly higher than those in a susceptible strain, and decreases in CYP6CX4 and GSTs2 expression resulted in a significant increase in mortality rate in response to flupyradifurone treatment [34]. CYP4C64 was strongly overexpressed in thiamethoxam-resistant strains, and knocking down CYP4C64 significantly reduced B. tabaci resistance to thiamethoxam. A T206A mutation in the 5′ untranslated region (UTR) enhanced CYP4C64 expression in thiamethoxam-resistant strains [37]. The expression levels of several other P450 genes are correlated with neonicotinoid treatment; for example, CYP4CS3, CYP6CX5, and CYP6DW2 were significantly up-regulated in imidacloprid- and acetamiprid-tolerant B. tabaci strains [32]. Activities of carboxylesterase (CarE) and GST were also reportedly related to thiamethoxam resistance [38,39], indicating that B. tabaci resistance to neonicotinoid insecticides may be a combined result of the activities of multiple detoxification enzymes rather than a single enzyme.

2.5. Biogenic Insecticide

Avermectins are a class of antibiotic insecticides produced as specialized metabolites by Streptomyces; the avermectin compound abamectin is widely used across China and remains an effective pesticide for B. tabaci control in most regions [19]. For many years, abamectin displayed high toxicity to B. tabaci MEAM1 (B) and MED (Q). Continuous selection in the laboratory revealed that the development of abamectin resistance in B. tabaci was relatively slow [40]. Until 2018, nearly all tested field strains displayed no resistance to abamectin [12,14,23,25]. However, in 2016–2017, MEAM1 (B) and MED (Q) collected from Shandong Province displayed moderate resistance to abamectin, suggesting that some populations may have an increased chance of developing resistance [19]. Furthermore, the eggs and larvae of laboratory strains showed higher resistance to abamectin than adults [25]. A new semi-synthetic antibiotic insecticide, emamectin benzoate, is highly effective, with increased efficiency and decreased toxicity compared to avermectin. Field strains from Fujian Province showed low resistance to emamectin benzoate [15]. Field strains from multiple regions in China showed minimal or no resistance to another new biogenic insecticide, spinosad, or its derivative, spinetoram [12,15,41]. In general, biological insecticides show promise as efficient insecticides for the control of field populations of B. tabaci in China. However, although abamectin resistance development is slow, the risk of increased resistance should still be addressed. Another new biogenic insecticide, afidopyropen, is a semi-synthetic derivative of pyripyropene A, a fermentation product of Aspergillus fumigatus Fresenius (Eurotiales: Trichocomaceae). Because it is an insecticide that has been used for a relatively short time in China, afidopyropen has been proven to have high toxicity against B. tabaci MEAM1 (B) and MED (Q) in all field populations tested [42]. Resistance selection experiments showed that resistance to afidopyropen in one strain was stably increased from the second to the sixth generation. Additionally, this resistance was subsequently stabilized between the seventh and tenth generations [43]. Thus, in contrast to abamectin, B. tabaci is expected to rapidly develop resistance to afidopyropen when exposed to this insecticide within several generations.
The enhanced metabolic detoxification systems found in insects may be the main reason for the observed resistance of B. tabaci to these insecticides. In an abamectin-resistant MEAM1 (B) strain, the oxidase inhibitor piperonyl butoxide (PBO) and the GST inhibitor diethyl maleate (DEM) produce significant synergistic effects on abamectin, indicating that enhanced metabolism mediated by P450 monooxygenase and GST activity, but not esterase activity, may be involved in abamectin resistance [40]. In an afidopyropen-resistant strain, PBO also showed significant synergism with afidopyropen, suggesting that oxidative metabolism may be one mechanism that results in afidopyropen resistance [43].

2.6. Other Insecticides

Cyantraniliprole is a second-generation anthranilic diamide product that provides cross-spectrum control of chewing and sucking insect pests. From 2012 to 2016, field populations collected from several regions in China showed little to no cyantraniliprole resistance [7,25]. However, since 2018, populations in some regions have begun to develop high resistance [10,18,44]. In one cyantraniliprole-resistant strain, P450 activity was markedly higher than that in susceptible strains, although esterase and GST activities were not significantly different between the two strains [44]. Fipronil is a phenylpyrazole insecticide, to which field populations in China have shown low to moderate resistance [12,15]. The major inhibitory neurotransmitter in insects is γ-aminobutyric acid (GABA); fipronil blocks a GABA-activated chloride channel, causing hyperexcitation and convulsions. Pymetrozine is a pyridine azomethine derivative, and resistance to this insecticide varies from low to high depending on the field populations sampled [11,18,19,28]. In the laboratory, pymetrozine resistance slowly increased from the first to the tenth generation, then rapidly increased from the eleventh to the eighteenth generation [45]. Long-term application of pymetrozine would, therefore, be expected to lead to rapid development of resistance in both MEAM1 (B) and MED (Q) populations. CYP6CM1 expression is closely related to pymetrozine resistance factors across B. tabaci populations [28].

2.7. Cross-Resistance

As mentioned above, insecticide resistance occurs via two distinct mechanisms: target-site point mutations and increased detoxification effects [33]. Insecticides that share target sites are more likely to form cross-resistance, but increased metabolic resistance may cause cross-resistance between different types of pesticides. An abamectin-tolerant B. tabaci strain showed obvious cross-resistance to the abamectin analogue, emamectin benzoate, and to imidacloprid, but not to fipronil [40]. Elevated metabolic detoxification is likely responsible for this cross-resistance because abamectin does not share target sites with imidacloprid. Cross-resistance to neonicotinoid insecticides is common. A thiamethoxam-resistant strain showed varying levels of cross-resistance to imidacloprid, acetamiprid, and nitenpyram, but not to abamectin or bifenthrin [38,39]. An imidacloprid-resistant strain showed high levels of cross-resistance to neonicotinoids, but not to cypermethrin or abamectin [31]. However, some neonicotinoid-resistant strains have displayed varying degrees of cross-resistance to other pesticides (such as abamectin and carbosulfan), which may be caused by elevated metabolic detoxification [38]. A flupyradifurone-resistant strain showed high cross-resistance to imidacloprid but no cross-resistance to thiamethoxam, acetamiprid, nitenpyram, or sulfoxaflor [34]. This suggests that the regulatory mechanisms used to resist damage caused by neonicotinoid insecticides are slightly different. A cyantraniliprole-resistant strain had no cross-resistance to imidacloprid, thiamethoxam, abamectin, sulfoxaflor, or bifenthrin [46]. A pymetrozine-resistant strain displayed low levels of cross-resistance to acetamiprid, imidacloprid, nitenpyram, and thiamethoxam, but no cross-resistance to abamectin or chlorpyrifos [45]. There was no cross-resistance between afidopyropen and pymetrozine in B. tabaci, even though these pesticides target the transient receptor potential vanilloid (TRPV) channel of insects, suggesting that afidopyropen may more effectively target the TRPV channel [42]. Furthermore, afidopyropen-resistant MED (Q) individuals showed significant cross-resistance to sulfoxaflor, but little cross-resistance to cyantraniliprole, flupyradifurone, imidacloprid, or thiamethoxam [43].
Table
Table 1. Reported insecticide resistance mechanisms of invasive Bemisia tabaci biotypes in China.
Table 1. Reported insecticide resistance mechanisms of invasive Bemisia tabaci biotypes in China.
InsecticideResistance
Mechanism		Associated GeneReferences
Organophosphates (ops)
Methamidophos
Phoxim
Chlorpyrifos
Profenofos
Acephate
Malathion		Target resistanceAcetylcholinesterase ace1 gene[14,18,20,21]
Pyrethroids
Bifenthrin
Cypermethrin		Target resistancePara-type voltage-gated sodium channel gene[14,18]
Neonicotinoids
Dinotefuran
Imidacloprid
Thiamethoxam
Acetamiprid
Sulfoxaflor
Flupyradifurone
Acetamiprid		Metabolic resistanceCytochrome P450 gene; glutathione-S-transferase gene (GST); nicotinic acetylcholine receptor β1 subunit gene (Btβ1); and ATP-binding cassette subfamily G member 3 gene (ABCG3)[8,9,18,28,29,32,33,34,35,39,47]
Biogenic insecticides
Abamectin
Afidopyropen		Metabolic resistanceCytochrome P450 gene and glutathione-S-transferase gene (GST)[40,48]
Other insecticides
Pymetrozine
Cyantraniliprole		Metabolic resistanceCytochrome P450 gene[28]

3. Management of B. tabaci Resistance

3.1. Insecticide Rotation

Rotating insecticides is the most effective method to delay the evolution of insecticide resistance and to regain pest susceptibility as part of an insecticide resistance management (IRM) program. Under pesticide selection pressure, B. tabaci resistance increases at different rates, depending on the pesticide. In the absence of a pesticide, resistance declines rapidly [30,43]. Selection of the most appropriate chemical insecticide for a given situation should take into consideration the available officially registered products and various parameters, such as crop stage, post-harvest interval, presence of beneficial insects or pollinators, pest infestation level, presence of other coexisting pests, and pesticide resistance history. The B. tabaci generation time ranges from 24 to 30 d; insecticides with different modes of action must, therefore, be rotated for field application every 30 d. All applications should strictly follow the relevant product label with regard to the rate, target pest, and the application method and frequency.

3.2. Improvement in Insecticide Efficiency

The development of insecticide resistance in pests is closely related to long-term and large-scale pesticide application [1,11]. The duration of use of a single insecticide can be interrupted by insecticide rotation, thus slowing the rate of resistance development [25,26]. Reducing the dosage of pesticide application can also decrease the development of resistance; to this end, some methods can be used to improve pesticide efficiency, such as the addition of synergists. The insecticide mixture approach has been thoroughly investigated in numerous pest systems, but it remains controversial. Therefore, the efficacy of mixing pesticides should continue to be assessed based on relevant research.

3.3. Synergists

Enzyme inhibitors may improve pesticide sensitivity in B. tabaci field populations to varying degrees [15]. Three common inhibitors have significant synergistic effects on pesticides: PBO, DEM, and the esterase inhibitor triphenyl phosphate (TPP). AChE activity is strongly inhibited by PBO, but not by TPP or DEM. In both laboratory and field strains of B. tabaci, GST activity is significantly inhibited in vivo by DEM [38]. Rational use of synergists can effectively improve the efficiency of some metabolizable insecticides; the effects of various synergists are closely related to pesticide metabolic mechanisms. PBO can play a synergistic role with numerous pesticides, such as thiamethoxam, imidacloprid, acetamiprid, cyantraniliprole, flupyradifurone, and afidopyropen [31,32,34,38,43,44]. This indicates that oxidases have a key role in the metabolism of many pesticides. Furthermore, TPP has significant synergism with thiamethoxam and chlorpyrifos, confirming that enhanced esterase activity is at least partially responsible for resistance to these pesticides [20,38].

3.4. Bacteriostatic and Insecticidal Compounds

Symbionts are ubiquitous in insects. Some participate in the synthesis of essential amino acids, forming a stable symbiotic relationship with the host [49]. The symbionts of various insects are known to improve host insecticide resistance through direct degradation or indirect regulatory mechanisms [50,51,52,53]. B. tabaci harbors the primary (P-) endosymbiont, Candidatus Portiera aleyrodidarum (Oceanospirillales), in bacteriocytes. Seven S-endosymbionts have also been identified to date, namely Hamiltonella (Enterobacteriaceae), Arsenophonus (Enterobacteriaceae), Wolbachia (Rickettsiales), Rickettsia (Rickettsiales), Cardinium (Bacteroidetes), Fritschea (Chlamydiales), and Hemipteriphilus (Proteobacteria) [54]. Several endosymbionts are reported to be associated with insecticide resistance in B. tabaci; however, the relevance of endosymbionts to pesticide resistance appears to vary between B. tabaci populations and to be dependent on the insecticide used [55,56]. Although the mechanism by which B. tabaci endosymbionts participate in the regulation of host pesticide resistance remains unclear, studies of similar systems have revealed relevant mechanisms in Riptortus pedestris [50], Bactrocera dorsalis [51], and Nilaparvata lugens [52]. Future research may uncover effective measures of decreasing B. tabaci insecticide resistance by regulating symbiotic bacteria, thereby providing novel strategies for managing B. tabaci resistance.

3.5. New Prevention and Control Technology

In recent years, pest control strategies based on RNA interference (RNAi) have been rapidly developed. RNA molecules used to control pests are called RNA-based pesticides; such RNAi agents can be used to inhibit or control agricultural pests by silencing the expression of important pest genes. RNA-based pesticides are single- or double-stranded polynucleotide segments that bind specific mRNAs corresponding to the target genes within a pest, causing transcript degradation or translation inhibition [57]. This interferes with normal growth of the target organism to minimize damage to the host plant. Compared with traditional small-molecule pesticides, RNA-based pesticides have several distinct advantages, including a strong target specificity, a lack of toxic residues (i.e., relative environmental safety), and a low development cost [58]. This method has been tested for B. tabaci control; RNAi of BtTPS1 and BtTPS2 significantly increased mortality and influenced the expression of target genes involved in energy metabolism and chitin biosynthesis in adults [59]. Nuclear receptors (NRs) play essential roles in diverse biological processes, such as insect metamorphosis. RNAi of some NRs causes malformation phenotypes in B. tabaci MED (Q), and several other NRs are potential targets for this pest control method due to their important roles in insect development [60]. Additionally, RNAi of genes related to pesticide resistance could promote pesticide sensitivity, thereby improving insecticide efficiency. For example, RNAi of CYP6CM1 is sufficient to increase imidacloprid sensitivity in a resistant strain [35]. Furthermore, RNAi of Inactive (Iav) together with Nanchung (Nan), a component of TRPV channel, increases MED (Q) sensitivity to afidopyropen [61]. Although RNAi technology is in development for commercial pest control, obstacles to its large-scale application remain. These include low efficiency of RNA delivery to target cells, low efficiency of target gene silencing, dose-limiting toxicity, insufficient interference efficiency, and low RNA molecule stability [62]. Despite these challenges, RNAi has tremendous potential for application in agricultural pest control.
At present, most pesticides in China are emulsifiable concentrates and wettable powders that have poor water dispersion, low biological activity, and low effective utilization [63]. The poor water solubility of most effective pesticide components is one of the most important factors inhibiting the improvement of effective pesticide utilization. Nano-pesticides are small in size but have large surface areas, and they can therefore improve water dispersibility and expand the contact area between pesticides and target pests, thereby increasing pesticide bioavailability. However, the small size, surface modifiability, and other desirable characteristics of nano-pesticides can also promote absorption and transport of these pesticides by plants; specifically, hydrophobic nano-pesticides may be absorbed during water uptake [64]. Leaf surfaces generally exhibit some hydrophobicity, which makes it difficult for pesticides to adhere; they tend to slide or wash off, minimizing pesticide application efficiency. Adding specific groups or changing the charge properties of nano-pesticides that have surface modifiability can enhance leaf adhesion [64]. Compared to traditional pesticides, nano-pesticides are, therefore, easier to keep in contact with plant leaves and stems, which prolongs the effective period and improves utilization. Furthermore, nanocarriers can effectively improve the environmental stability of active ingredients. They can also be used to build a controlled release system that responds to external pH, redox reactions, enzyme activity, light, temperature, or other factors, which can reduce the required dosage and frequency of pesticide application and increase the utilization rate. Although the safety of nano-pesticides for the environment and non-target organisms is unclear, they still represent a promising research area for pest control.

4. Conclusions

Two invasive B. tabaci biotypes, MEAM1 (B) and MED (Q), have rapidly spread in China. The speed of their spread is considered to be closely related to fitness costs, insecticide resistance, viral vector capacity, and host plant adaptation range. Chemical insecticides have served as the main method for controlling B. tabaci populations for many years, and they will likely remain so in the near future. Controlling the development and spread of pesticide resistance and improving insecticide efficiency will, therefore, be critical aspects of B. tabaci control in the future. MEAM1 (B) and MED (Q) populations had varying degrees of resistance to numerous traditional insecticides at the onset of their invasion of China. They have gradually developed additional resistance to new pesticides as such compounds are made available and applied in the field. Research into the resistance mechanisms used by B. tabaci in China has revealed several mutation sites related to OP and pyrethroid resistance. These mutation sites are now widely found throughout B. tabaci populations in China. Increases in detoxification enzyme activity have been established as key factors underlying most insecticide resistance, such as resistance to neonicotinoids. Insecticide rotation is a critical strategy to manage pesticide resistance. The continuous application of similar insecticides inevitably leads to rapid increases in insecticide resistance; conversely, reducing insecticide selection pressure will rapidly decrease resistance development. Rational use of synergists can also effectively improve pesticide efficiency and reduce the dosage required. Other pest control strategies, such as inhibiting resistance-promoting endosymbionts or using novel pesticides such as RNAi or nano-pesticides, are promising approaches currently in development for effective pest control.

Author Contributions

Conceptualization, Q.W., C.L. and R.W.; writing—original draft preparation, Q.W.; writing—review and editing, C.L. and R.W.; supervision, C.L. and R.W.; project administration, C.L. and R.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Natural Science Foundation of China (32172438, 31972266, 32272522) and the Outstanding Youth Foundation of the Beijing Academy of Agriculture and Forestry Sciences (YXQN202301).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All relevant data are available from the corresponding author on request ([email protected]).

Acknowledgments

We greatly appreciate Honglin Feng (Boyce Thompson Institute, Ithaca, NY, USA) for the critical instructions, and thank the anonymous reviewers and the editor for this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Recorded insecticide resistance cases among invasive Bemisia tabaci biotypes in China: (A) reported insecticide resistance cases by insecticide category, and (B) reported resistance cases in China over time.
Figure 1. Recorded insecticide resistance cases among invasive Bemisia tabaci biotypes in China: (A) reported insecticide resistance cases by insecticide category, and (B) reported resistance cases in China over time.
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Figure 2. Chemical structure of neonicotinoid insecticides applied in China: (A) chloronicotinyls; (B) thianicotinyls; (C) nitroguanidines; and (D) sulfoximines.
Figure 2. Chemical structure of neonicotinoid insecticides applied in China: (A) chloronicotinyls; (B) thianicotinyls; (C) nitroguanidines; and (D) sulfoximines.
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Wang, Q.; Luo, C.; Wang, R. Insecticide Resistance and Its Management in Two Invasive Cryptic Species of Bemisia tabaci in China. Int. J. Mol. Sci. 2023, 24, 6048. https://doi.org/10.3390/ijms24076048

AMA Style

Wang Q, Luo C, Wang R. Insecticide Resistance and Its Management in Two Invasive Cryptic Species of Bemisia tabaci in China. International Journal of Molecular Sciences. 2023; 24(7):6048. https://doi.org/10.3390/ijms24076048

Chicago/Turabian Style

Wang, Qian, Chen Luo, and Ran Wang. 2023. "Insecticide Resistance and Its Management in Two Invasive Cryptic Species of Bemisia tabaci in China" International Journal of Molecular Sciences 24, no. 7: 6048. https://doi.org/10.3390/ijms24076048

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