An isolate of Vibrio campbellii carrying the pir^VP gene causes acute hepatopancreatic necrosis disease

Abstract

Emerging Microbes & Infections (2017) 6, e2; doi:10.1038/emi.2016.131; published online 4 January 2017

Dear Editor,

In recent years, acute hepatopancreatic necrosis disease (AHPND) has rapidly spread in Asian countries and Mexico, causing severe mortality (up to 100%) and decreasing shrimp production.^{1, 2, 3, 4, 5, 6, 7, 8, 9} AHPND was originally shown to be caused by a specific virulent strain of Vibrio parahaemolyticus, namely the AHPND-causing V. parahaemolyticus (VP_AHPND).^{1, 5, 6} V. parahaemolyticus becomes virulent VP_AHPND after acquiring a plasmid (pVA1) expressing the deadly toxin Pir^VP, which consists of two subunits, PirA and PirB, and is homologous to the Pir (Photorhabdus insect-related) binary toxin.⁷ The plasmid pVA1 also carries a cluster of genes related to conjugative transfer; hence, this plasmid may potentially be able to transfer not only among V. parahaemolyticus strains but also to different bacterial species.^{7, 10} So far, there have been no published reports directly demonstrating that Vibrio campbellii can harbor pir^VP and cause AHPND in shrimp. In this paper, we challenged Litopenaeus vannamei with a strain of V. campbellii (20130629003S01) carrying pir^VP isolated from a L. vannamei farm and demonstrated that V. campbellii is a causative agent of AHPND.

In this paper, strain 20130629003S01 was isolated in June of 2013 from diseased L. vannamei in Guangxi, China. PCR and RT-PCR amplifications were performed using VpPirA and VpPirB primers specific to pir^VP genes (pirA and pirB).¹¹ The electrophoresis of PCR products showed that both pirA (284 bp) and pirB (392 bp) were detected in the strain (Figure 1A). A partial sequence of 16S rRNA was obtained by sequencing the PCR products obtained with primers 27F (5′-AGA GTT TGA TCC TGG CTC AG-3′) and 1492R (5′-TAC GGC TAC CTT GTT ACG ACT T-3′).¹² We found that strain 20130629003S01 belongs to the Vibrio core group, and its closest relatives are V. campbellii (99.72%) and V. rotiferianus (99.66%), according to the EzTaxon server (www.eztaxon-e.ezbiocloud.net). Partial sequences of σ⁷⁰ factor (rpoD), replication initiator protein (rctB) and toxin transcriptional activator (toxR) were amplified as described by Pascual et al.¹³ After alignment of sequences for 16S rRNA and the rpoD, rctB and toxR genes, the phylogenetic tree was constructed with concatenated sequences by using neighbor-joining analysis in MEGA 5 (Tempe, AZ, USA). The multilocus sequence analysis clearly identified strain 20130629003S01 as being the closest to V. campbellii (Figure 1B).

short-legendFigure 1.

Significantly, pir^VP genes were successfully amplified by using plasmid DNA extracted from the V. campbellii isolate (20130629003S01). In addition, next-generation sequencing of strain 20130629003S01 demonstrated that it also contains a pVA1-like plasmid containing pir^VP (unpublished data). Protein profiles of the crude protein fractions of strain 20130629003S01 were analyzed as described by Sirikharin et al.¹⁴ Analysis by SDS–polyacrylamide gel electrophoresis revealed two target bands at marker levels of ~17 kDa (PirA) and 50 kDa (PirB; Figure 1C). Mass spectrometry analysis followed by the MASCOT analysis revealed that the two proteins had similarity to the published protein sequences of PirA (gi|922664586) and PirB (gi|922664588) of V. parahaemolyticus M0605.

The pathogenicity of strain 20130629003S01 was examined in healthy L. vannamei shrimps weighing ∼1 g, which were reared in 90 l artificial seawater at salinity 30 in plastic tanks (density 15 shrimps/tank) at 27±2 °C. An immersion challenge was used to follow the bioassay protocol described by Tran et al.⁵ All experimental groups were assayed in triplicate. Shrimp immersed with the bacterial suspension began to develop typical gross signs of AHPND within 12 h, massive mortalities occurred from 12 h post challenge, and cumulative mortalities reached 100% within 36 h. Gross signs of challenged L. vannamei included an empty stomach and gastrointestinal tract as well as pale and atrophied hepatopancreas (Figure 1D). A histopathological examination of moribund shrimp revealed the presence of AHPND lesions (Figure 1E) characterized by the acute sloughing of hepatopancreatic tubule epithelial cells, some of which displayed intact organelles, such as nuclei and cytoplasmic vesicles (Figure 1E). To our knowledge, our study is the first to demonstrate that a V. campbellii strain carrying pir^VP causes AHPND. Therefore, AHPND caused by non-V. parahaemolyticus should be further investigated.

The shrimp farming industry is one of the important economic industries for countries in Asia and Latin America. AHPND is characterized by the acute and massive mortality in shrimp farms, causing severe production collapses and heavy economic losses. Ignoring the biosecurity of shrimp hatcheries and farms provides possibilities for the spread of VP_AHPND. The existence of pir^VP in non-V. parahaemolyticus isolates has been reported in a Vibrio harveyi-like stain from Vietnam¹⁵ and a Vibrio owensii-like from China.¹⁰ The present results may provide evidence for the horizontal transfer of the pir^VP gene or pVA1 plasmid between different bacterial species, thereby potentially increasing the complexity of causative agents of AHPND and aggravating the threat to the shrimp industry. On the basis of our finding that a V. campbellii carrying pir^VP causes AHPND, effective biosecurity measures should be considered to prevent the spread of AHPND in the future.

Acknowledgments

This work was supported by projects under the China Agriculture Research System (CARS-47), the Special Scientific Research Funds for Central Non-Profit Institutes, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences (Grant No: 20603022016012), the Construction Programme for ‘Taishan Scholarship’ of Shandong Province of China (S41201203) and the Project of the Aoshan Science and Technology Innovation Program of Qingdao National Laboratory for Marine Science and Technology (Grant No: 2015ASKJ02).