Citation: Mozumder, A.B.; Chanda,
K.; Chorei, R.; Prasad, H.K. An
Evaluation of Aluminum Tolerant
Pseudomonas aeruginosa A7 for In Vivo
Suppression of Fusarium Wilt of
Chickpea Caused by Fusarium
oxysporum f. sp. ciceris and Growth
Promotion of Chickpea.
Microorganisms 2022, 10, 568.
https://doi.org/10.3390/
microorganisms10030568
Academic Editor: Tim J. Dumonceaux
Received: 31 December 2021
Accepted: 7 February 2022
Published: 5 March 2022
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microorganisms
Article
An Evaluation of Aluminum Tolerant Pseudomonas aeruginosa
A7 for In Vivo Suppression of Fusarium Wilt of Chickpea
Caused by Fusarium oxysporum f. sp. ciceris and Growth
Promotion of Chickpea
Atifa Begum Mozumder , Kakoli Chanda, Ringhoilal Chorei and Himanshu Kishore Prasad *
Department of Life Science and Bioinformatics, Assam University, Silchar 788011, India;
atifamozumder@gmail.com (A.B.M.); kakolimic@gmail.com (K.C.); choreiringhoilal@gmail.com (R.C.)
* Correspondence: himanshu.k.prasad@aus.ac.in or himanshukprasad@gmail.com
Abstract: Chickpea wilt, caused by Fusarium oxysporum f. sp. ciceris, is a disease that decreases
chickpea productivity and quality and can reduce its yield by as much as 15%. A newly isolated,
moss rhizoid-associated Pseudomonas aeruginosa strain A7, demonstrated strong inhibition of Fusarium
oxysporum f. sp. ciceris growth. An in vitro antimicrobial assay revealed A7 to suppress the growth of
several fungal and bacterial plant pathogens by secreting secondary metabolites and by producing
volatile compounds. In an in vivo pot experiment with Fusarium wilt infection in chickpea, the
antagonist A7 exhibited a disease reduction by 77 ± 1.5%, and significantly reduced the disease
incidence and severity indexes. Furthermore, A7 promoted chickpea growth in terms of root and
shoot length and dry biomass during pot assay. The strain exhibited several traits associated with
plant growth promotion, extracellular enzymatic production, and stress tolerance. Under aluminum
stress conditions, in vitro growth of chickpea plants by A7 resulted in a significant increase in root
length and plant biomass production. Additionally, hallmark genes for antibiotics production were
identified in A7. The methanol extract of strain A7 demonstrated antimicrobial activity, leading to
the identification of various antimicrobial compounds based on retention time and molecular weight.
These findings strongly suggest that the strain’s significant biocontrol potential and plant growth
enhancement could be a potential environmentally friendly process in agricultural crop production.
Keywords: Fusarium oxysporum f. sp. ciceris; aluminum; biocontrol; chickpea; PGPR; Pseudomonas
aeruginosa A7
1. Introduction
Chickpeas (Cicer arietinum L.) are considered to be one of the oldest legumes known
from ancient times. Most likely, it originated in southeastern Turkey and Syria’s adjacent
areas [1]. Globally, it is a valuable crop and about 2.3 million tons enter the world market
annually [2]. The major chickpea legume grain-producing regions are in southern and
South-Eastern Asia, Africa, and Australia [2].
It is estimated that India produces 9.075 million tons of chickpeas annually, accounting
for 65% of the total production of chickpeas. The remarkable growth of chickpea pulse has
been documented in India, comprising the most significant production (47%; 10.90 MT)
among all pulse crops in 2019–2020 [2]. Chickpeas are sustainable legumes with nutritional
value for human and animal consumption as well as soil fertility. Chickpeas seeds and
leaves are an excellent source of carbohydrates, vitamins, fibers, and proteins. Chickpeas
play a leading role in food safety in the world by supplying the protein deficit of daily food
rations [3]. Chickpeas-based diets are recommended to combat lifestyle disease since they
contain several essential minerals such as calcium, phosphorus, iron, and zinc among other
substances, including phenolics and oligosaccharides [3]. There are numerous living and
Microorganisms 2022, 10, 568. https://doi.org/10.3390/microorganisms10030568 https://www.mdpi.com/journal/microorganisms