# HilE mediates motility thermoregulation in typhoidal Salmonella serovars at elevated physiological temperatures

## TL;DR

Typhoidal Salmonella strains reduce their movement at high body temperatures, and this is controlled by a protein called HilE, which may help prevent the spread of infection.

## Contribution

HilE is identified as a novel temperature-sensitive regulator of motility in typhoidal Salmonella, influencing host-pathogen interactions during fever.

## Key findings

- Typhoidal Salmonella represses motility at 39–40°C via HilE, unlike nontyphoidal strains.
- HilE regulates motility in a HilD-dependent manner, affecting flagellar gene expression.
- HilE absence increases uptake of S. Paratyphi A by human macrophages at high temperatures.

## Abstract

Salmonella enterica is a diverse bacterial pathogen consisting of both typhoidal and nontyphoidal clinically distinct serovars. While typhoidal serovars cause in humans a systemic life-threatening enteric fever, nontyphoidal Salmonella (NTS) usually provoke a localized self-limiting gastroenteritis. Factors responsible for the different diseases caused by distinct Salmonella serovars are still poorly understood. Here, we show that at elevated physiological temperature, manifested during enteric fever (39–40°C), the transcription of the flagellar regulon, its protein translation, and flagella-mediated motility are all repressed in the typhoidal serovar, S. Paratyphi A. In contrast, the NTS representative serovar, S. Typhimurium, maintains similar or even higher levels of flagellar genes transcription, translation, and motility at 40°C relative to 37°C. By using a temperature-responsive chromogenic reporter system in conjunction with a dense transposon mutagenesis screen we found that under elevated temperature, HilE negatively regulates S. Paratyphi A motility in a HilD-dependent manner. Because HilD is required for the transcriptional activation of flhDC, encoding the master regulator of the Salmonella flagellar-chemotaxis regulon, null deletion of hilE leads to motility upregulation at elevated temperature and the loss of motility thermoregulation in S. Paratyphi A. Moreover, we show that a HilE-mediated motility thermoregulation is common to other typhoidal serovars, including S. Typhi and S. Sendai, but not to S. Paratyphi B, nor to various NTS serovars. Interestingly, the absence of HilE also leads to a hyper-uptake of S. Paratyphi A by THP-1 human macrophages at 40°C, but not at 37°C. Based on these results, we propose that HilE plays a unique role in motility thermoregulation in typhoidal Salmonella in a way that may restrain systemic dissemination of the pathogen via professional phagocytes, during the acute phase of enteric fever.

Despite high genetic similarity, typhoidal and nontyphoidal Salmonella (NTS) strains of the single species Salmonella enterica cause in humans different diseases manifested as life-threatening enteric fever and short-term gastroenteritis, respectively. Currently, we are still ignorant about bacterial factors shaping the different lifestyles of typhoidal vs. NTS strains. Here we characterized differences in the regulation of Salmonella motility, which is an important virulence-associated phenotype, in response to changes in temperature, between typhoidal and NTS. We found that at elevated temperature, equivalent to the body temperature during enteric fever (39–40°C), the motility of typhoidal Salmonella, but not that of NTS is strongly repressed, by the negative regulator HilE in a HilD-dependent manner. Moreover, we demonstrate that HilE plays a previously unknown role in the interaction of S. Paratyphi A with phagocytic cells, as the absence of HilE caused enhanced uptake of this pathogen by human macrophages at elevated physiological temperature, but not at 37°C. Because motility thermoregulation by HilE was found in three different typhoidal serovars, but not in NTS, we hypothesize that motility regulation affects the interactions of Salmonella with its host and differences in its regulation contribute to the distinct pathogenicity of typhoidal vs. NTS strains.