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Applied Biotechnology & Bioengineering

Research Article Special Issue Plant Pathogenic Klebsiella pneumoniae

Biochemical characteristics of plant pathogenic Klebsiella Pneumoniae causing root bark necrosis and wilt in pomegranate

Ajayasree TS, Borkar SG

Department of Plant Pathology and Agricultural microbiology, Mahatma Phule Agricultural University, India

Correspondence: Ajayasree TS, Department of Plant Pathology and Agricultural Microbiology, Mahatma Phule Agricultural University, Rahuri-413722, Dist-Ahmednagar (MS), India

Received: June 08, 2018 | Published: July 25, 2018

Citation: Borkar SG, Ajayasree TS. Biochemical characteristics of plant pathogenic Klebsiella pneumoniae causing root bark necrosis and wilt in pomegranate. J Appl Biotechnol Bioeng. 2018;5(4):222-225. DOI: 10.15406/jabb.2018.05.00141

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Abstract

A plant pathogenic Klebsiella pneumoniae causing root bark necrosis and wilt in pomegranate was designated as Klebsiella pneumoniae strain Borkar by NCBI (accession number: KY941097.1) on the basis of 16s rRNA partial gene sequence submitted. This strain was studied for its biochemical characteristics as it was a new bacterial pathogen causing plant disease and its biochemical characteristics was compared with the known biochemical characteristics of other Klebsiella pneumoniae sub species and Klebsiella species.

The bacterium was positive for ONPG, lysine utilization, urease, vogus paskeur reaction, methyl red test, PYR, esculin hydrolysis, sorbitol, trehalose, malabiose, salicin, mannose, sucrose, glucose utilization, malonate, arabinose, rhamnose and mannitol utilization tests; whereas it was negative for ornithine utilization, Indole, β-glucoronidase, α- galactosidase, β- xylosidase, cellobiose, maltose, Raffinose, Lactose, H2S and Adonitol.

The plant pathogenic Klebsiella pneumoniae strain Borkar differed from Klebsiella pneumoniae in respect of sugar utilization. The plant pathogenic Klebsiella pneumoniae does not utilize α-galactosidase, β-xylosidase, cellobiose, maltose, Raffinose, Lactose whereas Klebsiella pneumoniae utilizes these sugars.

Similarly Plant pathogenic Klebsiella pneumoniae strain Borkar differed from Klebsiella oxycota, Klebsiella pneumoniae subsp. pneumoniae, Klebsiella rhizoscleronatis, Klebsiella ozaenae and Klebsiella terigena in one or the other known biochemical characteristics.

This opportunistic soil borne bacteria has emerged as a new soil borne plant pathogen particularly on pomegranate crop. Barring one example of its infection on maize this bacterial species is new one to cause infection in the plant. The genus Klebsiella is not yet included as a genus of plant pathogenic bacteria. Therefore we propose to include the genus Klebsiella as a plant pathogen and its biochemical characteristics are described in this paper.

Keywords: biochemical tests, klebsiella sp, plant pathogenic klebsiella pneumoniae, pomegranate pathogen

Introduction

Biochemical characterization is an important tool to differentiate the bacterial genus into species and subspecies.1 The individual bacterial species and subspecies are specific in the utilization or non-utilization of particular chemical molecules. Klebsiella pneumoniae is generally a serious human pathogen causing respiratory tract infection, loss of breathing leading to pneumonia and death of patient.2 This bacterial pathogen is also known to cause infection in animals particularly in dogs and pre-weaned pigs3‒6 and in birds also.7‒9 Immuno deficient animals, especially those with severe immune-deficiencies or defect in immune system, develop clinical disease symptoms associated with Klebsiella infection.

In 2016 the bacterium Klebsiella pneumoniae was reported to infect maize plant in China causing bacterial top rot disease of maize in Yunnan province.10 In subsequent year, its involvement as plant pathogen causing root bark necrosis and wilt in pomegranate was detected in pomegranate orchard of Mahatma Phule Agricultural University, Rahuri, India.11 The differentiation system of plant pathogenic Klebsiella pneumoniae species from other Klebsiella pneumoniae subspp is not available in the literature, since Klebsiella pneumoniae is recently reported as a plant pathogen. It is very necessary to characterize this plant pathogenic Klebsiella pneumoniae from other Klebsiella pneumoniae subspp and species. As the differentiation of species and subspp is generally based on biochemical tests, these were used to characterize the plant pathogenic Klebsiella pneumoniae strain Borkar, so as to differentiate it from the other known Klebsiella pneumoniae and Klebsiella species.

Materials and methods

Biochemical characterization of plant pathogenic Klebsiella pneumoniae strain borkar

Rapid biochemical identification test kits of Himedia viz. KB002 (HiAssortedTM), KB001 (Hi/MViCTM), KB003 (Hi25TM) and KB016 (Hi24TM) were used for biochemical characterization of Klebsiella pneumoniae strain Borkar.

A total 35 biochemical tests included in these identification test kit were used. These tests were ONPG, lysine utilization, ornithine utilization, urease, phenyl alanine deamination, Voges proskauer, Methyl red, indole, PVR, β-glucoronidase, α-galactosidase, β-xylosidase, esculin hydrolysis, sucrose, sorbitol, trehalose, glucose, cellobiose, melibiose, salicin, mannose, raffinose, lactose, TDA, nitrate reduction, H2S, citrate utilization, malonate, arabinose, xylose, adonitol, rhamnose, saccharose and mannitol. Each biochemical test kit is a standardized colorimetric identification system utilizing conventional biochemical test and carbohydrate utilization tests. The tests are based on the principle of pH change and substrate utilization. On inoculation with the bacterial culture in test kit media and incubation, the test media undergoes changes, due to metabolic activity of bacteria, which are indicated by a colour change in the media that are interpreted visually or after addition of the respective test reagent after incubation period.

The test kit was opened aseptically by peeling off the sealing tape. Each well of the test kit was inoculated with a loop of 24hour old bacterial culture by stab inoculation method and covered with peel off sealing tape. The kits were incubated at 35-37°C temperature for 24hours. The results were interpreted as per the standards given in the result interpretation chart. Addition of reagents wherever necessary was done to obtain the test results after the incubation period. The results are presented in the tabular form.

Results

Metabolic activity and utilization of different substrates by plant pathogenic Klebsiella pneumoniae strain Borkar

The bacterium was positive for ONPG, lysine utilization, urease, vogus paskeur reaction, methyl red test, PYR, esculin hydrolysis, nitrate reduction, citrate utilization and utilization of sucrose, sorbitol, trehalose, malatiose, salicin, mannose, glucose, malonate, arabinose, rhamnose and manitol as carbohydrate sugar, while it was negative for ornithine utilization, indole, H2S, β-glucoronidase, α-galactosidase, and β-xylosidase and did not utilize cellobiose, maltose, raffinose, lactose and adonitol as carbohydrate sugar (Table 1). This plant pathogenic Klebsiella pneumoniae strain Borkar was different in some of the biochemical characters to other Klebsiella pneumoniae and its subspecies (Table 2A‒2f).

Sr. No.

Metabolic activity/ utilization of substrate

Reaction of Klebsiella pneumoniae strain Borkar

1

ONPG

+

2

Lysine utilization

+

3

Ornithine utilization

4

Urease

+

5

Phenyl alanine deamination

v/─

6

VP

+

7

MR

+

8

Indole

9

PYR

+

10

β-glucoronidase

11

α-galactosidase

12

β-xylosidase

13

Esculin hydrolysis

+

14

Sucrose

+

15

Sorbitol

+

16

Trehalose

+

17

Glucose

+

18

Cellobiose

19

Melibiose

+

20

Salicin

+

21

Mannose

+

22

Maltose

23

Raffinose

24

Lactose

25

Nitrate reduction

+

26

H2S

27

Citrate utilization

+

28

Malonate

+

29

Arabinose

+

30

Adanitol

31

Rhamnose

+

32

Mannitol

+

Table 1 Metabolic activity and utilization of different substrates by plant pathogenic Klebsiell pneumoniae strain Borkar

+ = Positive, V = 11-89% positive, ─ = negative

Sr. No.

Metabolic activity/ utilization of substrate

Klebsiella pneumoniae

Klebsiella pneumoniae strain borkar

1

MR

V

+

2

Maltose

+

3

Raffinose

+

4

Lactose

+

Table 2 Variable characteristics of Klebsiella pneumoniae strain Borkar with comparison to other Klebsiella species

  1. Variation in biochemical characteristics of Klebsiella pneumoniae strain Borkar with Klebsiella pneumoniae

Sr No.

Metabolic activity/ utilization of substrate

Klebsiella oxycota

Klebsiella pneumoniae strain Borkar

1

Indole

+

2

α-galactosidase

+

3

β- Xylosidase

+

4

Cellobiose

+

5

Maltose

+

6

Raffinose

+

7

Lactose

+

8

Adonitol

+

  1. Variation in biochemical characteristics of Klebsiella pneumoniae strain Borkar with Klebsiella oxycota

Sr. No.

Metabolic activity/ utilization of substrate

Klebsiella ozaenae

Klebsiella pneumoniae strain Borkar

1

Lysine utilization

V/─

+

2

Urease

+

3

VP

+

4

α-galactosidase

+

5

β- Xylosidase

V

6

Sucrose

+

7

Sorbitol

V

+

8

Cellobiose

+

9

Maltose

+

10

Lactose

V

11

Nitrate reduction

V

+

12

Citrate utilization

V

+

13

Adonitol

+

  1. Variation in biochemical characteristics of Klebsiella pneumoniae strain Borkar with Klebsiella ozaenae

Sr. No.

Metabolic activity/ utilization of substrate

Klebsiella pneumoniae subsp. pneumoniae

Klebsiella pneumoniae strain Borkar

1

MR

V

+

2

α-galactosidase

+

3

β- Xylosidase

+

4

Cellobiose

+

5

Maltose

+

6

Raffinose

+

7

Lactose

+

8

Adonitol

+

  1. Variation in biochemical characteristics of Klebsiella pneumoniae strain Borkar with Klebsiella pneumoniae subsp. pneumoniae

Sr. No.

Metabolic activity/ utilization of substrate

Klebsiella rhizoscleronatis

Klebsiella pneumoniae strain Borkar

1

ONPG

+

2

Lysine utilization

+

3

Urease

+

4

VP

+

5

β- Xylosidase

V

6

Esculin hydrolysis

V

+

7

Sucrose

V

+

8

Cellobiose

+/V

9

Maltose

+

10

Raffinose

+

11

Citrate utilization

+

12

Adonitol

+

  1. Variation in biochemical characteristics of Klebsiella pneumoniae strain Borkar with Klebsiella rhizoscleronatis

Sr. No.

Metabolic activity/ utilization of substrate

Klebsiella terigena

Klebsiella pneumoniae strain Borkar

1

Ornithine utilization

V

2

Urease

+

3

MR

V

+

4

Raffinose

+

5

Lactose

+

  1. Variation in biochemical characteristics of Klebsiella pneumoniae strain Borkar with Klebsiella terigena

Discussion

The biochemical characteristics in bacteria are an important tool in their identification. Klebsiella pneumoniae, is a known important human pathogen causing pneumonia, nosocomical infection, urinary tract infection and infection of respiratory tract2 and fatal to human being.12 Klebsiella pneumoniae infection is also reported in animals and birds leading to severe enteritis, septicaemia and death.3,7 The strain of Klebsiella pneumoniae is also reported to infect maize plant in Yunnan province, China10 and recently in India on pomegranate crop causing wilt.11 The known biochemical characteristics of Klebsiella pneumoniae subspp and Klebsiella species was compared with plant pathogenic Klebsiella pneumoniae strain Borkar for its biochemical characteristics.

The plant pathogenic Klebsiella pneumoniae strain Borkar was positive for ONPG, lysine utilization, urease, VP, MR, PYR, esculin hydrolysis, nitrate reduction, citrate utilization and utilization of sucrose, sorbitol, trehalose, malatiose, salicin, mannose, glucose, malonate, arabinose, rhamnose and manitol as carbohydrate sources, while it was negative for ornithine utilization, Indole, H2S, β-glucoronidase, α-galactocidase, β-xylosidase and did not utilize cellobiose, maltose, raffinose, lactose and adonitol.

Plant pathogenic Klebsiella pneumoniae strain Borkar was different from previously reported Klebsiella pneumoniae in utilization of at least three sugars viz, maltose, raffinose and lactose. Plant pathogenic Klebsiella pneumoniae strain Borkar did not utilized these sugars whereas Klebsiella pneumoniae utilizes these.

Klebsiella pneumoniae is also reported to be associated with plant root system, probably as nitrogen fixer in maize, poa and wheat,13,14 but not yet reported as soil borne plant pathogen. Though Huang et al.10 reported Klebsiella pneumoniae causing bacterial top rot disease of maize; it was not described as soil borne plant pathogen. Klebsiella pneumoniae strain Borkar, is a soil borne plant pathogen infecting pomegranate plant by causing root bark necrosis and wilt in the plant. This pathogen under our experimentation did not infect the maize plant causing top rot and therefore, seems to be different strain of Klebsiella pneumoniae reported from China. Thus plant pathogenic Klebsiella pneumoniae strain Borkar is different Klebsiella species and not reported earlier. The biochemical characteristics of this strain certainly differentiate it from other Klebsiella pneumoniae sub spp.

Conclusion

Plant pathogenic Klebsiella pneumoniae strain Borkar can be differentiated from other known Klebsiella pneumoniae species on the basis of various biochemical tests. This opportunistic soil borne bacteria has emerged as a new soil borne plant pathogen particularly on pomegranate crop. Barring one example of its infection on maize this bacterial species is new one to cause infection in the plant. The genus Klebsiella is not yet included as a genus of plant pathogenic bacteria. Therefore we propose to include the genus Klebsiella as a plant pathogen and its biochemical characteristics are described in this paper.

Acknowledgments

None.

Conflict of interest

The author declares that there is no conflict of interest

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