The bacterium
Natranaerobius thermophilus
is an extremely halophilic alkalithermophile that can thrive under conditions of high salinity (3.3–3.9 M Na
+
), alkaline pH (9.5), and elevated temperature (53°C). To understand the molecular mechanisms of salt adaptation in
N. thermophilus
, it is essential to investigate the protein, mRNA, and key metabolite levels on a molecular basis. Based on proteome profiling of
N. thermophilus
under 3.1, 3.7, and 4.3 M Na
+
conditions compared to 2.5 M Na
+
condition, we discovered that a hybrid strategy, combining the “compatible solute” and “salt-in” mechanisms, was utilized for osmotic adjustment dur ing the long-term salinity adaptation of
N. thermophilus
. The mRNA level of key proteins and the intracellular content of compatible solutes and K
+
support this conclusion. Specifically,
N. thermophilus
employs the glycine betaine ABC transporters (Opu and ProU families), Na
+
/solute symporters (SSS family), and glutamate and proline synthesis pathways to adapt to high salinity. The intracellular content of compatible solutes, including glycine betaine, glutamate, and proline, increases with rising salinity levels in
N. thermophilus
. Additionally, the upregulation of Na
+
/ K
+
/ H
+
transporters facilitates the maintenance of intracellular K
+
concentration, ensuring cellular ion homeostasis under varying salinities. Furthermore,
N. thermophilus
exhibits cytoplasmic acidification in response to high Na
+
concentrations. The median isoelectric points of the upregulated proteins decrease with increasing salinity. Amino acid metabolism, carbohydrate and energy metabolism, membrane transport, and bacterial chemotaxis activities contribute to the adaptability of
N. thermophilus
under high salt stress. This study provides new data that support further elucidating the complex adaptation mechanisms of
N. thermophilus
under multiple extremes.
IMPORTANCE
This study represents the first report of simultaneous utilization of two salt adaptation mechanisms within the
Clostridia
class in response to long-term salinity stress.