Review Article - (2021) Volume 12, Issue 12
Application of the Lectin and Non-lectin Genes in Transgenic Crops
Suliman Khan1*,
Zou Xiaobo1,
Khalilur Rahman2,
Rahim Dost Khan2,
Muhammad Irfan3 and
Mariam Jamiel3
1Department of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013, China
2Department of Biotechnology, Abdul Wali Khan University Mardan, Mardan-23200, Pakistan
3Industrial Biotechnology Division, National Institute for Biotechnology and Genetic Engineering, Constituent College of Pakistan Institute of Engineering and Applied Sciences, PO Box 577, Jhang Road, Faisalabad, Pakistan
*Correspondence:
Suliman Khan, Department of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013,
China,
Tel: +251 912870382,
Email:
Received: 03-Oct-2021
Published:
30-Dec-2021
Abstract
Agricultural and horticultural crops are attacked by a number of pests, the most common of which are insect
mites and nematodes, which cause damage to the plants both directly and indirectly via the fungal, bacterial, or
viral infections they spread. Traditionally, agrochemicals (pesticides) were used to protect crops from pests, which
had negative effects on crop yield as well as contaminating our air, affecting plant, animal, and human health.
Transgenic crops that are resistant to major insect pests were one of the first achievements of plant biotechnology
as a result of insects' ability to develop resistance to single insecticidal gene products. Plant with single insecticide Bacillus thuringiensis and lectin genes with resistance to major pests of rice, Maize, Tobacco, and Cotton, made up the
first generation of products. The objective of this review was to discuss the application, potential, and limitation of
different insect-resistant genes in transgenic crops.
Keywords
Bacillus thuringiensis; Lectin; Pest; Transgenic plant
Introduction
One of the most common and controversial biotechnology
applications is transgenic crops [1,2]. To decrease dependency
on insect killer sprays, researchers genetically engineered cotton
and corn plants to manufacture insect killer proteins determined
by genes from the communal bacterium Bacillus thuringiensis (Bt)
[3]. These Bt proteins kill some of the world's most deadly insect
pests while causing minimal maltreatment to other animals, as well
as humans. 4.5 out of 10 Bt crops have many benefits, including
decreased pesticide use, pest control, defense of advantageous
natural competitors, improved yield, and higher agronomist
income [4,5]. Bt crops have been cultivated on more than 420M
hectares worldwide, up from 1.1M hectares in 1996 to 66 million
hectares in 2011. Bt corn reported for 67% of corn planted in the
US in 2012. Biotech Crops, Bt cotton reported for 79–95% of
cotton planted in US, India, China and Australia between 2010
and 2012. The notable capability of insects to respond to pesticides
and other control measures confirms the supposition that pest
adaptation poses the greatest risk to the success of Bt crops [6-9].
Pollutants resultant from bacterium, Bt Berliner are present in
all insect resistant transgenic crops currently on the market [10],
but transgenic crops expressing plant-derived proteins, Snowdrop
lectins Galanthus nivalis agglutinin (GNA) are currently being studied. GNA is à lectin that binds alpha-D-mannose specifically
and is toxic to a variety of insect pests from various orders, including
Homoptera, Coleoptera, and Lepidoptera [11]. Potato, tobacco,
wheat, rice, and sugarcane are among the crop species for which
transgenic lines expressing GNA have been created. According to
reports, most lectin genes have different levels of gene expression
to cop various abiotic pressures, such as cold, heat, drought,
and salinity [12]. Both lectin genes encoded by the rice, soybean
and Arabidopsis genomes were recognized and characterized
[13]. However, there is no comprehensive review article that has
summarized combine the application, limitation and potential of
the lectins and Bt genes in different transgenic plant.
Literature Review
Lectins application in transgenic crops
Plant lectins have also been effectively used to protect crops from
pest vermin [14,15]. Coleoptera, Lepidoptera, and Diptera have
also been found to be toxic to lectins [15]. Used Plant lectins
to fight sap-feeding insects going to the Hemiptera direction,
which contains around the world's record dangerous vermin.
Lectins allow nutrient interest to be blocked or midgut cells to be
impaired by facilitating phagocytosis and potentially other lethal metabolites found in the hindgut. Other non-Bt genes and Plant
lectins have been shown to be effective against sucking insect pests
in transgenic crops (Figure1a-d). Plant-derived RNA interference
(RNAi) technology has occurred as a new prospect in the fight
against insects, particularly in the fight against resistance in
targeted insect pests, as an alternative to conventional methods of
attaining resistance, such as the use of lectins, poisonous proteins
or inhibitors [16]. RNAi was first discovered in Caenorhabditis
elegant [17] and has since proved to be an effective gene silencing
mechanism in a number of organisms [18].
Toxicity of plant lectins towards mammals
Many plant lectins are present in a wide range of vegetables/crops
(e.g. tomato, potato, pea, bean, garlic, leek, lentil, soybean, peanut,
rice, corn, wheat) and fruits (e.g. banana, mulberry, breadfruit),
and are consumed by humans and animals on a regular base.
Since many of these plants are eaten raw, these plant lectins are
considered to be non-toxic for humans and mammals in general.
However, some legume lectins e.g. Concanavalin A (ConA) and
Phytohaemagglutinin (PHA) are known to be toxic for mammals
[19]. For example, PHA was shown to be toxic for humans
especially when kidney beans were not sufficiently cooked before
consumption. The acute symptoms of PHA poisoning are nausea,
vomiting or diarrhea and are most likely due to the ability of PHA
to bind to the epithelial cells from the digestive tract which can
cause changes in cellular morphology and metabolism. It should be
noted that several lectins will survive digestion by gastrointestinal
enzymes. Consequently, the interaction of these plant lectins with
glycoproteins in the digestive tract was reported to result in both
local and systemic reactions [19]. Although toxicity was clearly
shown for the broad bean (P. vulgaris) lectin considerable variation
in lectin activity was observed for different beans [20]. Interestingly,
the bioactivity of some plant lectins against mammalian tissues and
cells could also be exploited for other applications, e.g. the use of
plant lectins as potential anticancer drugs [20]. Other well-known
examples of plant lectins with a severe toxicity towards mammals are
ricin and abrin present in castor beans (R. communis) and the seeds
of Abrus precatorius (jequirity bean), respectively [21]. However, it
should be mentioned that not all ricin-B lectins are equally toxic as
ricin and abrin. It has been clearly shown that ricin-B lectins from
elderberry (Sambucus sp.) can be considered as virtually non-toxic
compared to ricin [22]. Lectins related to the snowdrop lectin GNA
have been studied in detail for their activity on insects. One of the major reasons for this large interest in GNA-related lectins is that
several of these lectins are found in edible plants (e.g. leek, garlic),
which will reduce the problems related to consumer acceptability
whenever these lectins would be used in crop plants. A report by
Fenton B, et al. [23] reported the binding of the snowdrop lectin to
human white cells. However, these data are contradicted by other
studies reporting very low if any mitogenic and immunogenic
activity of GNA [24,25]. Since the proliferative response of the
GNA-related lectin from daffodil was shown to be age-related
with weak mitogenicity observed for adult human lymphocytes
but more than sevenfold increased effects on lymphocytes from
umbilical cord blood, it is important to check different age groups
when testing the response of lectins on cells [26]. Obviously, health
safety assessment for each lectin is necessary before plant lectins
could be introduced into crop plants for commercial purposes.
In a 90-day feeding study with rats designed to assess the safety of
genetically modified rice expressing the kidney bean lectin PHA-E,
clear abnormalities were observed in rats after PHA-E ingestion
[27]. In contrast, a similar 90- day feeding study using transgenic
rice expressing GNA revealed no adverse effects on rats after
continuous dietary GNA uptake [28].
Worldwide Bt crops to pest resistance
Recent biotechnology breakthroughs have had a significant effect
on agricultural crops improvement by integrating genes from
different origins to establish insect pest resistance [28]. Pest vermin
and pathogens, as previously said, are significant intimidations to
crops, causation a 37% loss of productivity, with 13% of that loss
due solely to pest vermin [29]. Since 1996, protected transgenic
crops from pests, also recognized as Bt crops, have been cultivated
all over the world, proving to be effective at managing pest
vermin and dropping the use of toxic pesticides [30,31] (Figure 1 and Table 1).
Insecticidal proteins produced by Bt bacteria are identified as Cry
toxins because they form mineral presences. Based on primary
sequence similarities, Cry toxins are grouped into fifty-four types
(Cry1–Cry54) and various subtypes (e.g., Cry1Ba and Cry1Aa).
They are particularly specialized in which they solitary affect a few
insects, including lepidopteron, coleopterans, and dipterans, as
well as nematodes [32,33]. Although here are other families of Cry
proteins that are not 3D-Cry, the three domain (3D)-Cry family
is a wide group of Cry-toxins with members that are similar in
sequence and structure. Contempt the high amount of Cry toxins,
only a few hundred are commercially available as sprays or in Bt crops (Cry1Ac, Cry1Ab, Cry1Aa, Cry1F, Cry1E, Cry1D, Cry1C,
Cry3B, Cry3A, Cry2Ab, Cry2Aa, and Cry34/Cry35/33) (Table 2).
Figure 1: Transformation steps to generate potential transgenic maize plantlets. a) Germinating immature maize embryos after co-cultivation with
Agrobacterium harboring pCAMBIA-UASAL recombinant plasmid, b) Maize transformants growing in test tubes, c) Hardening of transformed maize
plantlets in soil pots and later in greenhouse and d) Hardening of transformed maize plantlets in soil pots and later in greenhouse.
Crops |
Gene |
Application |
Method |
References |
Cotton |
Bt Vip3Aa |
Against major insects |
Agrobacterium-mediated genetic alteration |
50 |
Bamboo |
Dirigent-jacalin |
Resistance to biotic and
abiotic stresses |
Agrobacterium-mediated genetic alteration |
51 |
Rice |
GNA |
Against the insect |
Agrobacterium-mediated genetic alteration |
52 |
Rice |
ASAL |
Sap-feeding insects |
Agrobacterium-mediated genetic alteration |
53 |
Tobacco |
ASAL |
Homopteran insects |
Agrobacterium-mediated genetic alteration |
54 |
Maize |
GNA |
Aphids |
Agrobacterium-mediated genetic alteration |
55 |
Wheat |
Pap |
Wheat Aphids |
Biolistic alteration |
56 |
Tobacco |
lec-s |
Pathogens and pests |
Agrobacterium-mediated genetic alteration |
57 |
Tobacco |
ASAL, ASAII |
Cotton leaf worm |
Agrobacterium-mediated genetic alteration |
58 |
Wheat |
GNA |
Aphid Sitobion avenae |
Biolistic alteration |
59 |
Potato |
GNA |
Aphids |
Agrobacterium-derived genetic alteration |
49 |
Maize |
ASAL |
Sap-feeding insects |
Agrobacterium-derived genetic alteration |
60 |
Onion |
GNA |
Aphid Colonization |
Agrobacterium-derived genetic alteration |
61 |
Potato |
ConA |
Peach-potato aphid |
Agrobacterium- derived genetic alteration |
62 |
Wheat |
GNA |
Grain aphid |
Biolistic |
59 |
Maize |
GNA |
Corn leaf aphid |
Agrobacterium-derived genetic alteration |
54 |
Chickpea |
ASAL |
Cowpea aphid |
Agrobacterium- derived genetic alteration |
63 |
Cotton |
ACA |
Cotton aphid |
Agrobacterium- derived genetic alteration |
64 |
Cotton |
ASAL |
Jassid and whitefly |
Agrobacterium-derived genetic alteration |
65 |
Indian mustard |
ASAL |
ACA (Amaranthus caudatus agglutinin) ACA-ASAL |
Agrobacterium- derived genetic alteration |
66 |
Indian mustard |
(ACA-SAL) |
Giving resistance against mustard aphid by reducing survival and fecundity |
Agrobacterium-mediated genetic transformation of the apical meristem |
60 |
Table 1: Plant lectins have been used in a number of ways to cultivate insect-resistant crops. Pests that have been addressed as well as transition methods are explored. White backed plant hopper (WBPH), Brown plant hopper (BPH), small brown plant hopper (SBPH) and green leaf hoppers (GLH) are the four types of plant hoppers.
S.No |
Crop |
Toxin |
Country |
Y. marketed |
Dose |
Insects |
References |
1 |
Corn |
Cry1Ab |
S.africa |
1998 |
Low |
B. fusca |
67, 68 |
2 |
Corn |
Cry1Ab |
USA |
1996 |
Low |
H. zea |
69, 70 |
3 |
cotton |
Cry2Ab |
India |
2006 |
Low |
P. gossypiella |
71 |
4 |
Corn |
Cry1A105 |
Argentina |
2010 |
Low |
D. saccaharalis |
72, 73 |
5 |
Corn |
Cry1F |
USA |
2003 |
Low |
S. prugiperda |
74, 75 |
6 |
Corn |
Cry1A.105 |
USA |
2010 |
Low |
H. zea |
76 |
7 |
Corn |
Cry3Bb |
USA |
2003 |
Low |
D. v. virgifera |
77, 78 |
8 |
Corn |
Cry1F |
Brazil |
2009 |
Low |
S. prugiperda |
79, 80 |
9 |
Cotton |
Cry2Ab |
USA |
2003 |
Low |
H. zea |
69, 81 |
10 |
Corn |
eCry3.Ab |
USA |
2014 |
Low |
D. v. virgipera |
82, 83 |
11 |
Cotton |
Cry1Ac |
USA |
1996 |
Low |
H. zea |
69, 70 |
12 |
Corn |
Cry1Ab |
Brazil |
2008 |
Low |
S. prugiperda |
84 |
13 |
Corn |
Cry34/35Ab |
USA |
2006 |
Low |
D. v. virgipera |
78, 85 |
14 |
Cotton |
Cry1Ac |
India |
2002 |
Low |
P. gossypiella |
86, 87 |
15 |
Corn |
mCry3A |
USA |
2007 |
Low |
D. v. virgipera |
78, 88 |
16 |
Corn |
Cry1Fa |
USA |
2003 |
Low |
S. albicosta |
89, 90 |
17 |
Cotton |
Cry2Ab |
Australia |
2004 |
High |
H. armigera |
91, 92 |
19 |
Cotton |
Cry1Ac |
Brazil |
2013 |
Low |
C. includes |
93, 94 |
20 |
Cotton |
Cry1Ac |
USA |
1996 |
High |
H. virescens |
70, 95 |
21 |
Corn |
Cr1Ab |
Spain |
1998 |
High |
S. nonagroides |
96 |
22 |
Cotton |
Cry1Ac |
China |
2000 |
High |
P. gossypiella |
97 |
23 |
Corn |
Cry1Ac |
USA |
1999 |
Low |
D. grandiosella |
98, 99 |
24 |
Corn |
Cry1Ab |
Spain |
1998 |
Low |
O. nubilalis |
99, 100 |
25 |
Cotton |
Cry1Ac |
Australia |
1996 |
Low |
H. armigera |
101, 102 |
26 |
Cotton |
Cry1Ab |
USA |
2003 |
High |
P. gossypiella |
103, 104 |
27 |
Cotton |
Cry1Ac |
China |
2000 |
High |
O. nubilalis |
105, 106 |
28 |
Cotton |
Cry1Ab |
Australia |
2004 |
High |
H. armigera |
91, 92 |
29 |
Cotton |
Cry1Ac |
Mexico |
1196 |
Low |
H. virescens |
95 |
30 |
Cotton |
Cry1Ac |
USA |
1996 |
High |
P. gossypiella |
104 |
31 |
Cotton |
Cry1Ac |
Australia |
1996 |
Low |
H. punctigera |
104 |
32 |
Corn |
Cry1Fa |
USA |
2003 |
Low |
O. nubilalis |
105, 106 |
33 |
Corn |
Vi3pA |
Brazil |
2010 |
High |
S. frugiperda |
107 |
34 |
Corn |
Cry1Ab |
USA |
1196 |
Low |
O. nubilali |
108, 109 |
Table 2: Practical resistant Bt crops.
Limitation and risk of insect’s resistance transgenic crops
Plant biotechnology has made significant progress in recent years, posing both prospects and threats. Transgenic and non-transgenic
crops are grown in close vicinity. Insect movement from scattered
arenas to transgenic crops may occur, and the increased pest weight
that results can perimeter the benefits of transgenic crops. For
several years, Bt toxins have been commonly used as “natural”
pesticides, with no evidence of insect species developing resistance
of their own [34]. Though, with the rapid rise in the prevalence
of Bt toxins in the environment (due to transgenic crops), insect
species could be under more strain to develop resistant biotypes.
The indication on these problems is still unsatisfying, and careful
monitoring is needed before large-scale transgenic crop deployment
under subsistence farming conditions. One strategy for addressing
these issues is to create a new group of transgenic with improved
genes and to use gene groupings to slow down the emergence of
resistance in insect inhabitants.
(1) Concert limits
(2) Secondary pest complications
(3) Insect compassion
(4) Progress of evolution and resistance of new biotypes
(5) Ecological effects on gene expression
(6) Gene leak into the atmosphere
(7) Possessions on non-target organisms and
(8) Bio-safety of food from transgenic crops are all issues that
bound the utility of transgenic crops for pest control [34].
Plant genetic transformation Procedure, methods and
their limitation
Plant genetic transformation Procedure, methods and their
limitation: Indirect and direct transformation are the two most
popular approaches for genetic transformation [35]. Indirect
methods, which use bacteria, are discussed to as biological, whereas
direct approaches, which depend on the dispersion of the cellular
wall, are referred to as physical. Even though indirect approaches
are still more common for plant alteration than direct approaches,
physical approaches have lately become more popular. Indirect
transition strategies use bacteria skilled of passing genes to higher
plant species to insert plasmids, which are isolated circular DNA
molecules present in bacteria that are distinct from the chromosome
of bacteria into the target cell. Agrobacterium rhizogenes and
Agrobacterium tumefaciens, two soil innate bacteria, are the most
commonly used microorganisms [36-40] and [41,42]. A plasmid used for transformation can be somewhere between 5 and 12 kb
pairs in size [43]. Plasmids contain several genes, pretend similarly
to bacterial chromosomes, and are self-replicating means that they
can reproduce independently inside the host. A single cell may
contain up to fifty plasmids. Agrobacterium (Ag) can transmit an
oncogene plasmid to its host and promote tumor growth [43-50].
This stuff (plasmid) has been used as a biotic path for genetic plant
transformation, but the oncogene has been deleted (deactivated)
from existing vectors, so they are no longer capable of inducing
tumors. Despite its problems with regeneration of certain plants,
Ag has been common in the industry [51-65] since the first active
gene supplement in the 1980s [66-77]. It is broadly used for a
variety of applications, but it is incomplete by the low competence
of Ag transformation, mainly in monocot such as mueslis [78- 85]. Furthermore, Ag can familiarize vector sequences that aren't
needed for transformation but may have unintended consequences
in the plant [85-109].
Conclusion
In this study, the applications, limitations and potentials of the
lectins and non lectins genes worldwide in transgenic plants were
discussed. Traditional plant breeding played an important role in
crop improvement in previous decades, but the introduction of
genetic engineering technology revolutionized breeding methods by
breaking down hybridization barriers between species and genera.
The 36th anniversary of transgenic technologies for the production
of genetically engineered plants is approaching. Insect pests have
had a major impact on the production of farm crops all over the
world. In terms of crop production and economic benefits to
farmers, the commercialization of insect-resistant crops expressing
Bt and lectin genes has been excellent. It's worth noting that almost
all commercially available insect-resistant crops carry Bt genes. In
light of the increased production of insect resistance, it is critical to
look at other causes of pest resistance in addition to implementing
resistance-delaying strategies.
Significance Statement
This manuscript thoroughly covers the applications and
importance of the lectins, the genes associated with these proteins
and as discussed as prospective biocontrol gene targets in the
efforts to make transgenic plants. Different variants of the lectins
are produced/synthesized by the plants in different organs most
specifically seeds, roots and leaves which are primary targets of the
different insects and pathogens. Recombinant DNA technology could be employed to produce transgenic plants which will not
only protect plants but also be helpful to minimize the toxic effects
of agrochemicals on soil and environment.
Conflicts of Interest
There are no conflicts of interest declared by the writers.
Contribution of author
Conceptualization and Writing of the original draft S.K, Revision
and editing of the final version K.U.R, R.D.K, Z.Z, M.I, M.J and
M.I, supervision, Z.X. All authors have read and agreed to the
published version of the manuscript.
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Citation: Khan S, Xiaobo Z, Rahman K, Dost Khan R, Irfan M, Jamiel M, et al. (2021) Application of the Lectin and Non-lectin Genes in Transgenic Crops. J Plant Pathol Microbiol. 12:590.
Copyright: © 2021 Khan S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.