The Scientific World JournalVolume 2012 (2012), Article ID 130136, 6 pagesdoi:10.1100/2012/130136

Research Article

Antibiotic Resistant Salmonella and Vibrio Associated with Farmed Litopenaeus vannamei

Sanjoy Banerjee,¹ Mei Chen Ooi,² Mohamed Shariff,1,2 and Helena Khatoon¹

¹Institute of Bioscience, Universiti Putra Malaysia, Selangor, 43400 Serdang, Malaysia²Faculty of Veterinary Medicine, Universiti Putra Malaysia, Selangor, 43400 Serdang, Malaysia

Received 21 November 2011; Accepted 28 December 2011

Academic Editors: J. Qiu and G. Salvat

Copyright © 2012 Sanjoy Banerjee et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Salmonella and Vibrio species were isolated and identified from Litopenaeus vannamei cultured in shrimp farms. Shrimp samples showed occurrence of 3.3% of Salmonella and 48.3% of Vibrio. The isolates were also screened for antibiotic resistance to oxolinic acid, sulphonamides, tetracycline, sulfamethoxazole/trimethoprim, norfloxacin, ampicillin, doxycycline hydrochloride, erythromycin, chloramphenicol, and nitrofurantoin. Salmonella enterica serovar Corvallis isolated from shrimp showed individual and multiple antibiotic resistance patterns. Five Vibrio species having individual and multiple antibiotic resistance were also identified. They were Vibrio cholerae (18.3%), V. mimicus (16.7%), V. parahaemolyticus (10%), V. vulnificus (6.7%), and V. alginolyticus (1.7%). Farm owners should be concerned about the presence of these pathogenic bacteria which also contributes to human health risk and should adopt best management practices for responsible aquaculture to ensure the quality of shrimp.

1. Introduction

Shrimp is an important commodity in the global fishery trade due to its increasing demand and competitive international price [1]. As a result of rising shrimp exports, traditional shrimp farming which began in Malaysia in the 1930s has given way to intensive farming system. At present, the bulk of the production consists of Litopenaeus vannamei having a production of 52,926 tonnes [2]. It has been introduced in the early 2000 due to the advantages in terms of disease management and most widely cultured in intensive system throughout Malaysia for local consumption as well as for export.

With the change to intensive culture system having high stocking density, disease problems appear frequently causing heavy economic losses to the industry. Antibiotics are normally used to prevent or treat disease outbreaks in shrimp farming [3]. However, extensive use of antibiotics in shrimp farming can cause the development of antibiotic-resistant pathogens which can infect both cultured animals as well as humans [4, 5].

Shrimp intended for export have to meet the bacteriological standards of the importing countries. Salmonella and Vibrio species are important foodborne pathogens and most importing countries do not accept them in raw frozen shrimp. Contamination of tropical shrimp with Salmonella due to growth in polluted waters has been a problem in many parts of the world and is reported to be a part of the natural population of the brackishwater cultured shrimp [6]. In the United States, most Salmonella contamination problems in seafood were in shrimp [7]. In addition, opportunistic Vibrio spp. is the most common bacterial pathogen found in shrimp which can cause lethal infections following primary infections with other pathogens, environmental stress, nutritional imbalance, and/or predisposing lesions [8]. In humans, Vibrio spp. are known to cause gastroenteritis, cholera, and septicemia [9].

Therefore, the present study was carried out in major shrimp producing areas to identify the incidence of Salmonella and Vibrio in Litopenaeus vannamei cultured in commercial shrimp farms and their resistance to some of the commonly used antibiotics in aquaculture.

2. Materials and Methods

2.1. Sampling

Clinically healthy with no external lesions or clinical signs and alive L. vannamei were collected from three farms from growout ponds (80–120 days; total 6 ponds) situated in Carey Island (2°52′0′′ N, 101°22′0′′ E) and Kuala Selangor (3°21′0′′ N, 101°15′0′′ E), Malaysia. The live shrimp were transported in oxygenated pond water filled plastic bags and put into another plastic bag filled with ice flakes and placed in styrofoam boxes. Water samples from ponds were collected in sterile bottles and transported in ice. Samples were transported to the Aquatic Animal Health Unit in Universiti Putra Malaysia and processed immediately for examination. The three farms had well laid out ponds and had characteristics as shown in Table 1.

Table 1: Characteristics of the three farms from where shrimp and water were sampled.

Farm 1
Farm 2
Farm 3

Average pond size (ha)
0.4
0.4
0.4

Stocking density (PL/m²)
80
80
80–100

Age of farm (years)
13
16
10

Number of ponds
20
14
52

Source of water
Brackish water river
Brackish water river
Brackish water sea

Use of antibiotics
No
No
No

Use of probiotics
No
Yes
Yes

Source of feed
Direct-feed miller
Direct-feed miller
Direct-feed miller

Nearby farms
No
Chicken farm
Shrimp farm

Market
Local
Local, export
Local, export

2.2. Bacterial Isolation

2.2.1. Shrimp Sample

For isolation of Salmonella, the head and exoskeleton of shrimp were removed aseptically. Muscle and intestine (10 g) were separately taken aseptically from the shrimp, placed in individual sterile test tubes, and homogenized in 3 mL autoclaved seawater using stomacher for 1 m. The homogenized sample was incubated in buffered peptone water at 37°C for 24 h for preenrichment. Selective enrichment was done using 10 mL of Rappaport and Vassiliadis (RVS) broth (Merck, Germany) inoculated with 1 mL culture from buffered peptone water and incubated at 42°C for 24–48 h. A loopful of sample from RVS was then streaked on selective media xylose-lysine-tergitol 4 (XLT-4) (Merck, Germany) and brilliant-green phenol-red lactose sucrose (BPLS) agar (Merck, Germany) and incubated at 37°C for 24–48 h. Subculture on XLT-4 and BPLS was done to obtain pure culture. Salmonella spp. colonies appear black or black-centered on XLT-4 and red centered pink on BPLS.

For isolation of Vibrio from shrimp, one loopful of haemolymph was taken from hepatopancreas and cultured in thiosulphate citrate bile salt sucrose (TCBS) agar (Merck, Germany) with 3% sodium chloride (NaCl) (Merck, Germany). The culture was incubated at 25°C for 18 to 24 h. Yellow and green single colonies were subcultured on TCBS and tryptic soy agar (TSA) (Merck, Germany) with 3% NaCl at 25°C for 24 h to obtain pure culture.

2.2.2. Water Sample

Pond water (10 mL) was diluted with 90 mL buffered peptone water and processed according to shrimp samples for isolation of Salmonella. In the case of Vibrios, pond water was plated on TCBS agar using the spread plate technique and processed according to shrimp samples.

2.3. Bacterial Identification

Different biochemical tests such as triple sugar iron (TSI), urease test, lysine iron agar (LIA), sulfide indole motility (SIM), slide agglutination test, and Salmonella serotyping were performed for identification of Salmonella spp.

Vibrio species identification was done using API 20E (bioMérieux, France) identification system. Escherichia coli (ATCC 25922) was used as control. Gram staining was also done from single pure culture colony.

2.4. Antibiotic Sensitivity Test

Antibiotic susceptibility test was conducted using disc diffusion method on Mueller Hinton agar at 37°C for 24 h. Procedure was based on the standardized disc agar diffusion method of the National Committee for Clinical Laboratory Standards for antimicrobial susceptibility tests [10]. After incubation, the diameter of the zone of inhibition was measured and compared with BBL zone interpretative chart to determine the sensitivity of the isolates to the antibiotics. The BBL zone interpretative chart was used in the absence of standard interpretative scheme for environmental isolates or for shrimp pathogens. The antimicrobials oxolinic acid 2 μg (OA 2), compound sulphonamides 300 μg (S3 300), tetracycline 30 μg (TE 30), sulfamethoxazole 23.75 μg/trimethoprim 1.25 μg (SXT 25), norfloxacin 10 μg (NOR 10), ampicillin 10 μg (AMP 10), doxycycline hydrochloride 30 μg (DO 30), and erythromycin 15 μg (E 15) were selected as they are veterinary important antimicrobials. Chloramphenicol 30 μg (C 30) and nitrofurantoin 300 μg (F 300) were also included since they were in use few years ago. The antimicrobials were from Oxoid, UK.

3. Results

3.1. Bacterial Isolation and Identification

3.1.1. Shrimp and Water Samples

One Salmonella and five Vibrio spp. were isolated and identified from shrimp and water samples. Salmonella enterica serovar Corvallis was isolated from water sample in Farm 1 and shrimp samples from Farm 2 and 3. However, five Vibrio spp., namely, V. alginolyticus, V. cholera, V. mimicus, V. parahaemolyticus, and V. vulnificus were isolated from both shrimp and water samples from all the three farms (Table 2). Farm 1 and 3 had low occurrence of Vibrio spp., while Farm 2 had moderate to high occurrence. The overall occurrence of Salmonella and Vibrio in shrimp was 3.33% and 48.3%, respectively.

Table 2: Percentage (%) of Salmonella and Vibrio spp. in three farms isolated from shrimp and water.

Isolated bacteria
Farm 1
Farm 2
Farm 3

Shrimp
Water
Shrimp
Water
Shrimp
Water

Salmonella enterica Serovar Corvallis
0
Yes
10

3.3

Vibrio mimicus
15
Yes
40
Yes
10

Vibrio vulnificus
5

20

3.3
Yes

Vibrio cholera
0
Yes
60
Yes
16.67
Yes

Vibrio parahaemolyticus
0

0

20
Yes

Vibrio alginolyticus
0

0

3.3

Isolates from water did not state percentage as only one sample was taken per pond to determine if the bacteria isolated came from water.

3.2. Antibiotic Sensitivity Test

The Salmonella enterica serovar Corvallis isolates from water in Farm 1 and shrimp in Farm 3 were found to be resistant to erythromycin only. However, the two S. enterica serovar Corvallis isolates from shrimp in Farm 2 were found to be resistant to all antibiotics except for nitrofurantoin and norfloxacin (Table 3).

Table 3: Susceptibility (zone of inhibition in mm) of Salmonella and Vibrio species isolated from different shrimp farms to antibiotics.

Isolates
NOR 10
DO 30
E 15
SXT 25
F 300
S3 300
AMP 10
OA 2
C 30
TE 30

Farm 1

Shrimp
V. mimicus (S1)
S-31
S-24
MS-18
S-26
S-25
S-20
R-6.5
S-29.5
S-31
S-23.5

V. mimicus (S2)
S-31
S-23
MS-19
S-24.5
S-23
S-30
R-6
S-28
S-32
S-22

V. mimicus (S3)
S-28
S-17
MS-20
S-22
S-22
S-28
MS-16
S-22.5
S-29
MS-18

V. vulnificus
S-18
S-21
MS-18.5
S-23.5
S-23
S-30
R-7
S-28
S-30
S-24

Water
Salmonella
S-40
S-21
R-12
S-18
S-24
S-30
S-24
S-26
S-26
MS-17

V. cholerae (S1)
S-31
S-18.5
MS-20
S-24
S-23
S-24
R-6
S-30
S-31
S-20

V. cholerae (S2)
S-26
S-22
MS-16
S-25
S-27.5
S-26
R-6
S-29
S-32
S-23

V. mimicus
S-29.5
S-17
MS-20.5
R-6
S-23
R-6
R-7.5
S-25.5
S-29.5
R-13

Farm 2

Shrimp
Salmonella (S1)
S-26
R-6
R-6
R-6
S-20
R-6
R-6
R-6
R-6
R-6

Salmonella (S2)
S-28.5
R-8
R-6
R-6
S-21
R-6
R-6
R-6
R-6
R-6

V. cholerae (S1)
S-29
R-9
MS-18
S-24
S-23.5
S-28
R-6
S-27
S-30
R-14

V. cholerae (S2)
S-29
R-10
MS-16
S-23.5
S-21
S-22
MS-13.5
S-28.5
S-28
R-11.5

V. cholerae (S3)
S-32
R-10.5
MS-18
S-27
S-24
S-25
R-6
S-30.5
S-31.5
R-10.5

V. cholerae (S4)
S-29
S-20
MS-19.5
S-22.5
S-22
MS-15
R-7.5
S-27.5
S-31
S-19

V. cholerae (S5)
S-26.5
MS-14
MS-17.5
S-22.5
S-21.5
S-27
R-7
S-24.5
S-32
MS-16

V. cholerae (S6)
S-24
S-18
MS-16.5
S-20.5
S-20
S-27
R-6
S-24
S-29
MS-16

V. mimicus (S1)
S-29
S-23
MS-18
S-24
S-24
S-22
R-6
S-29.5
S-35
S-25

V. mimicus (S2)
S-28
S-22
MS-20
S-22
S-24.5
S-28
R-6
S-27
S-32
S-24

V. mimicus (S3)
S-27.5
S-18.5
MS-20
S-25
S-24
S-31
R-13
S-29
S-31
S-21.5

V. mimicus (S4)
S-26
S-21
MS-18.5
S-23
S-23.5
S-30
R-6
S-25
S-30
S-22

V. vulnificus (S1)
S-28
MS-14
MS-19
S-24
S-22
S-28
R-8
S-25
S-30
MS-18

V. vulnificus (S2)
S-26
S-20
MS-18.5
S-23
S-21.5
S-26
R-7.5
S-29
S-31
S-23

Water
V. cholerae
S-30
S-21
MS-20
S-26
S-23
S-22
R-8
S-28.5
S-30
S-19.5

V. mimicus
S-27
S-16.5
MS-19.5
S-22.5
S-22.5
MS-14
R-6
S-24
S-29.5
S-20.5

Farm 3

Shrimp
Salmonella (S1)
S-42
MS-15
R-10
S-25
S-23
S-20
S-26
S-28
S-25
S-20

Salmonella (S2)
S-41
MS-13
R-10
S-27
S-21.5
S-20
S-26
S-27.5
S-25
MS-17

V. alginolyticus
S-23
S-24
MS-17
S-20.5
S-23
S-17
R-6
S-22
S-32
S-24

V. cholerae (S1)
S-25
S-24
MS-20
S-24
S-25
S-26
R-6
S-22
S-31
S-25

V. cholerae (S2)
S-24
S-22.5
MS-19
S-22.5
S-24
S-25
R-6
S-19
S-30.5
S-25

V. cholerae (S3)
S-21
MS-13
MS-16
S-22
S-22
S-27
R-7.5
S-27
S-26.5
R-14

V. cholerae (S4)
S-24
S-19.5
MS-17.5
S-24
S-21
S-25
R-6
S-27.5
S-27
S-20.5

V. cholerae (S5)
S-25
S-18
MS-15.5
S-23.5
S-19
S-24
R-6
S-27
S-26.5
S-21

V. mimicus (S1)
S-27
S-22
MS-17
S-25
S-21.5
S-21
R-9
S-26.5
S-30
S-23

V. mimicus (S2)
S-26
S-20
MS-17.5
MS-15
S-22
S-19.5
R-8
S-26.5
S-25
S-20

V. mimicus (S3)
S-25
S-20
MS-16
S-18
S-18
S-25
R-10
S-24
S-28
S-21.5

Water
V. parahaemolyticus (S1)
S-28
S-23.5
MS-19
S-25
S-22
S-23.5
R-6
S-28
S-31
S-24.5

V. parahaemolyticus (S2)
S-23
S-20.5
MS-17
S-21.5
S-20
S-25
R-8
S-25
S-30
S-21

V. parahaemolyticus (S3)
S-24
S-22
MS-17
S-24
S-21
S-20
R-7.5
S-25
S-29
S-21.5

V. parahaemolyticus (S4)
S-24
S-20.5
MS-16.5
S-21
S-20
S-19
R-9
S-24.5
S-30
S-20

V. parahaemolyticus (S5)
S-22.5
S-18
MS-16.5
S-23
S-20
S-26
R-8.5
S-22
S-26.5
S-20

V. parahaemolyticus (S6)
S-23
S-17.5
MS-18
S-20.5
S-19.5
S-25
R-12.5
S-23
S-28.5
S-20

V. vulnificus (S1)
S-22.5
S-21
MS-17.5
S-22
S-24
S-22.5
R-6
S-22.5
S-28
S-21.5

V. vulnificus (S2)
S-26
S-18.5
MS-16.5
S-16
S-22
S-26.5
R-9
S-27
S-28
S-20

V. cholerae
S-30
S-26
S-24
S-27.5
S-30
S-28
R-7
S-25.5
S-33
S-28

V. parahaemolyticus (S1)
S-29
S-23
MS-19.5
S-25
S-24
S-23.5
R-6
S-28
S-30
S-24

V. parahaemolyticus (S2)
S-26
S-20
S-27.5
S-22.5
S-21
S-17
R-9
S-25
S-30
S-20.5

V. vulnificus
S-34
S-30
S-24
S-36
S-32
S-40
R-10
S-30
S-40
S-34

NOR 10: norfloxacin 10 μg; DO 30: doxycycline hydrochloride 30 μg; E 15: erythromycin 15 μg; SXT 25: sulfamethoxazole 23.75 μg/trimethoprim 1.25 μg; F 300: nitrofurantoin 300 μg; S3 300: compound sulphonamides 300 μg; AMP 10: ampicillin 10 μg; OA 2: oxolinic acid 2 μg; C 30: chloramphenicol 30 μg; TE 30: tetracycline 30 μg; S: susceptible; MS: moderately susceptible; R: resistant.

In Farm 1, V. vulnificus and V. mimicus (S1, S2) isolated from shrimp were resistant to AMP 10. On the other hand, V. mimicus (S1, S2) isolated from water was resistant to SXT 25, S 300, and AMP 10, whereas V. cholerae (S1, S2) was resistant to AMP 10 only.

In case of Farm 2, V. cholerae (S1, S3) isolated from shrimp were resistant to DO 30, AMP 10, and TE 30, V. cholerae (S2) to DO 30 and TE 30, whereas V. cholerae (S4, S5, S6) were resistant to AMP 10. V. cholerae isolated from water was resistant to AMP 10 only. Besides, V. mimicus isolated from shrimp and water, and V. vulnificus isolated from shrimp were found to be resistant to AMP 10 also. In Farm 3, all the vibrios isolated from shrimp and water were resistant to AMP 10 (Table 3).

All Vibrio isolates except for two were resistant to ampicillin. Tetracycline was the second highest and doxycycline was the third highest that the Vibrio spp. were resistant to (Table 3). Farm 1 and 2 were found to have more antibiotic-resistant patterns (one to four antibiotics) than Farm 3 (one to two antibiotics). Out of the five Vibrio species, V. cholerae showed the most antibiotic-resistant pattern.

4. Discussion

Results of this survey showed that Salmonella and Vibrio isolated and identified from the three shrimp farms are a serious cause for concern since they are of public health significance. Salmonella is facultative anaerobes and belongs to the family Enterobacteriaceae, and more than 2500 serovars of Salmonella are considered potential pathogens in animal and human. Many Vibrio spp. are pathogenic to humans and have been implicated in foodborne disease.

Several studies have been done on prevalence of Salmonella in the tropics [11–13]. In the present study, Salmonella was found in water samples from Farm 1 and shrimp samples from Farm 2 and 3. This is in accordance with the studies where Salmonella have been reported from shrimp pond water [1, 12, 14] and shrimp [11, 12, 15]. Studies by Iyer and Varma [16], Bhaskar et al. [11], and Wan Norhana et al. [12] emphasized that Salmonella is natural part of the microflora of the shrimp culture practice. However, the absence of Salmonella from water and shrimp samples in some farms leading to a low occurrence in the present study could mean that Salmonella is not a common normal flora in shrimp culture environment. This is in accordance with a study done in Thailand by Dalsgaard et al. [17] who reported the absence of Salmonella from shrimp, sediment, water, and pelleted feed. Study by Koonse et al. [14] also showed that Salmonella is not part of the natural flora of the shrimp culture environment or naturally present in shrimp growout ponds. It is related to the concentration of fecal bacteria in the source of water supply to the growout pond water. In the present survey, the water source for two of the shrimp farms were from Langat River. The Langat River is one of the principal rivers draining a densely populated and developed area of Selangor. The major pollution sources affecting Langat River are sewage treatment plants, manufacturing industries not equipped with proper effluent treatment facilities, livestock, and pig farms [18]. Therefore, farmers should treat the water properly before introducing into the culture ponds.

In the present study, all S. enterica serovar Corvallis isolated from shrimp and water showed resistance to erythromycin. This is in agreement with the study done by Wan Norhana et al. [12] where S. enterica serovar Weltevreden, S. enterica serovar Hvittingfoss, S. enterica serovar Litchfield, S. enterica serovar Agona, S. enterica serovar Paratyphi, S. enterica serovar Benin, and S. enterica serovar Java isolated from shrimp were resistant to erythromycin. However, Salmonella isolated from Farm 2 showed multiple antibiotic resistances (eight antibiotics) compared to Farm 1 and 3 which were resistant to one antibiotic only. The occurrence of multiple antibiotic resistances could be due to the presence of chicken farm nearby that maybe using different types of antibiotics. Antibiotic is used in poultry as therapeutic as well as growth promotant. According to Singer and Hofacre [19], antibiotics and their metabolites as well as bacteria can spread from poultry farms into waterways. In addition, poultry litter can also help in their dissemination onto open field. Petersen et al. [20] have reported that integrated broiler chicken-fish farm contributed to antimicrobial-resistant bacteria in a pond environment. The antibiotic residues from the nearby chicken farm could have led to multiple antibiotic resistance observed in the present survey.

The natural occurrence of vibrios in marine and estuarine environment has been reported by Varnam and Evans [21]. Incidence of vibrios in marine-caught seafoods including shrimp has been reported by Adeleye et al. [22], while Boinapally and Jiang [23] showed that vibrios are also found in pond-reared shrimp.

In general, the incidence of bacteria resistance to shrimp samples was higher than those in water samples from the same location. In the present survey, differences in antibiotic resistance patterns in a species of Vibrio could be due to presence of different strains. Bacteria resistance to AMP10 was the highest followed by TE30. Ampicillin is not commonly used in shrimp culture. So there is a possibility that these vibrios could have acquired resistance from other places. The widespread use of tetracycline because of its low toxicity and broad-spectrum antibiotic activity against a wide range of Gram-positive and Gram-negative bacteria [24] and also as a successful prophylaxis and therapy against Vibrio [25, 26] could have led to high resistance.

In the present survey, although the managers of the farms stated that they did not use any antibiotics, the possibility of the presence of antibiotic-resistant bacteria in shrimp could be from postlarvae. Yasuda and Kitao [27] reported that Vibrio spp. were the dominant genera in the digestive tract of the zoea of Penaeus japonicus. According to Baticados and Paclibare [28], a variety of drugs are used in shrimp hatcheries. The use of these drugs leads to resistance to certain antimicrobials during the rearing of postlarvae in the hatchery which remain in the shrimp gut when transferred to the growout ponds [29].

The other possibility of the presence of antibiotic resistant bacteria could be the use of probiotics. According to Mathur and Singh [30], there are reports that commensal bacteria including lactic acid bacteria may act as reservoirs of antibiotic resistant genes that can be transferred to pathogenic bacteria. Therefore, the use of probiotics in the surveyed farms may have led to the incidence of multidrug resistant bacteria.

Four out of five Vibrio spp. isolated in the present study were similar to the findings of Bhaskar and Setty [31] who reported the presence of V. alginolyticus as the most common followed by V. cholerae, V. parahemolyticus, and V. vulnificus in P. monodon culture system. Farm 3 had two Vibrio species more than Farm 1 and 2 that had three species each. This could be because of the different source of postlarvae or different source of water. Farm 1 and 2 obtained postlarvae from the same hatchery and had the same source of water.

The result of this survey reveals the presence of multidrug resistant Salmonella and Vibrio in shrimp farms. Antibiotic resistance is a legitimate concern which may affect future therapy of shrimp and human disease. Farm owners should be concerned about the presence of these pathogenic bacteria which also contributes to human health risk and should adopt best management practices for responsible aquaculture to ensure the quality of shrimp.

Acknowledgment

The authors would like to thank the managers of the shrimp farms who have made the sampling possible.

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